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        <title>Breast Cancer Research and Treatment via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Breast Cancer Research and Treatment' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Breast+Cancer+Research+and+Treatment&t=Breast+Cancer+Research+and+Treatment&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 08 Feb 2012 08:41:17 +0100</lastBuildDate>
        <item>
            <title>Recommendations for the aesthetic evaluation of breast cancer conservative treatment</title>
            <link>http://www.medworm.com/index.php?rid=5666761&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw03442500hw62834%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;During the Turning Subjective Into Objective seminar held in Lisbon in May 2011, experts in the topic gathered to discuss
 the unsolved problems of aesthetic evaluation of breast-conserving treatment (BCT). The purpose of this study is to review
 the main methodological issues related to the aesthetic evaluation of BCT, to discuss currently used methods of evaluation
 and the lack of a gold standard, and to write a set of recommendations that can be used as guidance for the aesthetic evaluation
 of BCT.
 
 
	Content Type Journal ArticleCategory ReviewPages 1-9DOI 10.1007/s10549-012-1978-8Authors
		Maria João Cardoso, Breast Unit, Champalimaud Cancer Centre, Lisbon, PortugalJaime Santos Cardoso, INESC Porto Breast Research Group, Faculdade de Engenharia, Universidade do...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5666761</comments>
            <pubDate>Fri, 03 Feb 2012 17:52:07 +0100</pubDate>
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        <item>
            <title>Efficacy of zoledronic acid in postmenopausal Japanese women with early breast cancer receiving adjuvant letrozole: 12-month results</title>
            <link>http://www.medworm.com/index.php?rid=5666762&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl7q813q2854198p3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Aromatase inhibitor-associated bone loss has not been proved in the Japanese or Asian women. The aim of this study was to
 evaluate an upfront or delayed strategy of bone protection therapy with zoledronic acid administered at 4&amp;nbsp;mg every 6&amp;nbsp;months
 in postmenopausal Japanese women with early breast cancer to compare with results of the Z-FAST and ZO-FAST studies in western
 countries. Postmenopausal women with hormone receptor positive early breast cancer receiving adjuvant letrozole were randomly
 assigned to receive either upfront or delayed-start zoledronic acid (4&amp;nbsp;mg intravenously every 6&amp;nbsp;months). The delayed group
 received zoledronic acid when lumbar spine (L2–L4) bone mineral density (BMD) decreased to less than young adult mean −2.0SD or w...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5666762</comments>
            <pubDate>Fri, 03 Feb 2012 17:52:05 +0100</pubDate>
            <guid isPermaLink="false">5666762</guid>        </item>
        <item>
            <title>Favorable outcome associated with an IGF-1 ligand signature in breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5659404&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe9u268432063l220%2F</link>
            <description>In conclusion, a breast tumor-derived signature of high IGF-1 ligand is associated with favorable outcome, in contrast
 to a previously reported IGF-IR activation signature. The prognostic value of the IGF-I ligand signature is validated in three
 independent datasets. These signatures should be applied in study of IGF1-R targeted therapy.
 
 
	Content Type Journal ArticleCategory EpidemiologyPages 1-11DOI 10.1007/s10549-012-1952-5Authors
		Lina Mu, Department of Epidemiology and Public Health, Yale University School of Medicine, New Haven, CT 06520-8034, USADavid Tuck, Department of Pathology, Yale University School of Medicine, New Haven, CT 06520-8034, USADionyssios Katsaros, Gynecologic Oncology and Breast Cancer Unit, Department of Obstetrics and Gynecology, University of Turin, Turin...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5659404</comments>
            <pubDate>Wed, 01 Feb 2012 17:12:05 +0100</pubDate>
            <guid isPermaLink="false">5659404</guid>        </item>
        <item>
            <title>MUTYH gene variants and breast cancer in a Dutch case–control study</title>
            <link>http://www.medworm.com/index.php?rid=5659403&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn37868g5wk348352%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The MUTYH gene is involved in base excision repair. MUTYH mutations predispose to recessively inherited colorectal polyposis and cancer. Here, we evaluate an association with breast
 cancer (BC), following up our previous finding of an elevated BC frequency among Dutch bi-allelic MUTYH mutation carriers. A case–control study was performed comparing 1,469 incident BC patients (ORIGO cohort), 471 individuals
 displaying features suggesting a genetic predisposition for BC, but without a detectable BRCA1 or BRCA2 mutation (BRCAx cohort), and 1,666 controls. First, for 303 consecutive patients diagnosed before age 55&amp;nbsp;years and/or with
 multiple primary breast tumors, the MUTYH coding region and flanking introns were sequenced. The remaining subjects were genotyped for...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5659403</comments>
            <pubDate>Wed, 01 Feb 2012 17:12:05 +0100</pubDate>
            <guid isPermaLink="false">5659403</guid>        </item>
        <item>
            <title>Estimation of tamoxifen metabolite concentrations in the blood of breast cancer patients through CYP2D6 genotype activity score</title>
            <link>http://www.medworm.com/index.php?rid=5659406&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa73435r280207mh4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Tamoxifen, a prodrug used for adjuvant breast cancer therapy, requires conversion to the active metabolite endoxifen through
 CYP 2D6. We aimed to construct an algorithm to predict endoxifen concentrations based on a patient’s CYP 2D6 genotype, demographic
 factors, and co-medication use. Eighty-eight women enrolled in the UCSF TamGen II study and 81 women enrolled in a prospective
 study at Dana-Farber Cancer Institute were included in this analysis. All the women had been on tamoxifen for at least 3&amp;nbsp;months
 before blood collection. Demographic information included the patient’s age, race/ethnicity, body mass index (where available),
 and self-reported and measured medications and herbals that affect 2D6 activity. DNA was extracted and genotyped for 2D6 (Ampli...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5659406</comments>
            <pubDate>Tue, 31 Jan 2012 16:48:05 +0100</pubDate>
            <guid isPermaLink="false">5659406</guid>        </item>
        <item>
            <title>The miRNA-200 family and miRNA-9 exhibit differential expression in primary versus corresponding metastatic tissue in breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5659405&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fjgnr3k5616386174%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Metastases are the major cause of cancer-related deaths, but the mechanisms of the metastatic process remain poorly understood.
 In recent years, the involvement of microRNAs (miRNAs) in cancer has become apparent, and the objective of this study was
 to identify miRNAs associated with breast cancer progression. Global miRNA expression profiling was performed on 47 tumor
 samples from 14 patients with paired samples from primary breast tumors and corresponding lymph node and distant metastases
 using LNA-enhanced miRNA microarrays. The identified miRNA expression alterations were validated by real-time PCR, and tissue
 distribution of the miRNAs was visualized by in situ hybridization. The patients, in which the miRNA profile of the primary
 tumor and corresponding dist...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5659405</comments>
            <pubDate>Tue, 31 Jan 2012 16:48:05 +0100</pubDate>
            <guid isPermaLink="false">5659405</guid>        </item>
        <item>
            <title>Inactivation of GPR30 reduces growth of triple-negative breast cancer cells: possible application in targeted therapy</title>
            <link>http://www.medworm.com/index.php?rid=5647044&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9245m2v6r4494344%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Triple-negative breast cancers lack estrogen receptor α (ERα), progesterone receptor, and do not overexpress human epidermal
 growth factor receptor 2 (Her-2). They are neither susceptible to endocrine therapy nor to a therapy using the anti-Her-2
 antibody, trastuzumab. Therefore, an efficient targeted therapy is warranted. Triple-negative breast tumors frequently express
 membrane bound estrogen receptor G-protein coupled receptor (GPR30). As proof of principle, we analyzed the consequences of
 a knock-down of GPR30 expression on the growth regulation of triple-negative breast cancer cell lines. Cells of triple-negative
 breast cancer cell lines were transfected with siRNA against GPR30 or control siRNA, and cell growth was stimulated either
 with 10−9 M 17β-estr...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5647044</comments>
            <pubDate>Mon, 30 Jan 2012 16:07:44 +0100</pubDate>
            <guid isPermaLink="false">5647044</guid>        </item>
        <item>
            <title>Upper limb progressive resistance training and stretching exercises following surgery for early breast cancer: a randomized controlled trial</title>
            <link>http://www.medworm.com/index.php?rid=5647045&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F43n7v7r15367287k%2F</link>
            <description>In conclusion, a supervised exercise program provided some, albeit small, additional benefit
 at 6&amp;nbsp;months post-intervention to women who had been provided with written information and reminders to use their arm. Both
 the groups reported few impairments including swelling immediately following the intervention and 6&amp;nbsp;months post-intervention.
 Notably, resistance training in the post-operative period did not precipitate lymphedema.
 
 
	Content Type Journal ArticleCategory Clinical TrialPages 1-10DOI 10.1007/s10549-012-1964-1Authors
		Sharon L. Kilbreath, Faculty of Health Sciences, University of Sydney, P.O. Box 170, Lidcombe, Sydney, NSW 1825, AustraliaKathryn M. Refshauge, Faculty of Health Sciences, University of Sydney, P.O. Box 170, Lidcombe, Sydney, NSW 1825, AustraliaJane ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5647045</comments>
            <pubDate>Sat, 28 Jan 2012 16:51:29 +0100</pubDate>
            <guid isPermaLink="false">5647045</guid>        </item>
        <item>
            <title>Cyclooxygenase-2 expression in proliferative Ki-67-positive breast cancers is associated with poor outcomes</title>
            <link>http://www.medworm.com/index.php?rid=5647046&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu481345014g55642%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In order to investigate the implications of cyclooxygenase-2 (COX-2) expression in combination with Ki-67 on breast cancer
 outcomes, the COX-2 and Ki-67 expression levels and other clinicopathologic parameters were investigated in 861 breast cancers.
 Clinicopathological parameters and survival were investigated in association with the expression levels of both COX-2 and
 Ki-67 using univariate and multivariate analyses. COX-2 expression was positive in 493 (57.3%) of invasive tumors. COX-2 was
 associated with favorable markers, but was not related to survival outcome by itself. However, COX-2 in proliferative tumors
 [COX-2(+)/Ki-67(+)] were significantly associated with unfavorable factors and the worst survival, but COX-2 in non-proliferative
 tumors [COX-2(+)/Ki-6...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5647046</comments>
            <pubDate>Sat, 28 Jan 2012 06:42:12 +0100</pubDate>
            <guid isPermaLink="false">5647046</guid>        </item>
        <item>
            <title>Dose-dependent change in biomarkers during neoadjuvant endocrine therapy with fulvestrant: results from NEWEST, a randomized Phase II study</title>
            <link>http://www.medworm.com/index.php?rid=5647047&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Frwn23l411q13766l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;NEWEST (Neoadjuvant Endocrine Therapy for Women with Estrogen-Sensitive Tumors) is the first study to compare biological and
 clinical activity of fulvestrant 500 versus 250&amp;nbsp;mg in the neoadjuvant breast cancer setting. We hypothesized that fulvestrant
 500&amp;nbsp;mg may be superior to 250&amp;nbsp;mg in blocking estrogen receptor (ER) signaling and growth. A multicenter, randomized, open-label,
 Phase II study was performed to compare fulvestrant 500&amp;nbsp;mg (500&amp;nbsp;mg/month plus 500&amp;nbsp;mg on day 14 of month 1) versus fulvestrant
 250&amp;nbsp;mg/month for 16&amp;nbsp;weeks prior to surgery in postmenopausal women with ER+ locally advanced breast cancer. Core biopsies
 at baseline, week 4, and surgery were assessed for biomarker changes. Primary endpoint: change in Ki67 labe...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5647047</comments>
            <pubDate>Fri, 27 Jan 2012 17:55:30 +0100</pubDate>
            <guid isPermaLink="false">5647047</guid>        </item>
        <item>
            <title>Adherence and discontinuation of adjuvant hormonal therapy in breast cancer patients: a population-based study</title>
            <link>http://www.medworm.com/index.php?rid=5647048&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fgp6334425368v823%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Adherence to long-term pharmacological treatment for chronic conditions is often less than optimal. Till date, a limited number
 of population-based studies have assessed adherence to adjuvant hormonal therapy in breast cancer, a therapy with proven benefits
 in terms of reductions of recurrence and mortality. We aimed to examine rates of adherence and early discontinuation in Sweden
 where prescribed medications are subsidized for all residents and made available at reduced out-of-pocket costs. Individual-level
 data were obtained from Regional Clinical Quality Breast Cancer Registers, the Swedish Prescribed Drug Register, and several
 other population-based registers. Multivariate logistic regression was used to analyze factors associated with adherence to
 prescribed...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5647048</comments>
            <pubDate>Fri, 27 Jan 2012 17:55:29 +0100</pubDate>
            <guid isPermaLink="false">5647048</guid>        </item>
        <item>
            <title>Black–white differences in receipt and completion of adjuvant chemotherapy among breast cancer patients in a rural region of the US</title>
            <link>http://www.medworm.com/index.php?rid=5647049&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7802gk1lwm74457n%2F</link>
            <description>This article presents the first focused evaluation of black–white differences in receipt and
 completion of chemotherapy for breast cancer in a primarily rural region of the United States. We performed chart abstraction
 on initial therapy received by 868 women diagnosed with Stages I, IIA, IIB, or IIIA breast cancer in 2001–2003 in southwest
 Georgia (SWGA). For chemotherapy, information collected included treatment plan, dates of delivery, concordance between therapy
 planned and received, and date and reasons for end of treatment. The patient’s age at diagnosis, race, marital status, insurance
 coverage, hormone receptor status, comorbidities, socioeconomic status, urban/rural status, treatment site, and distance to
 the site were also collected. Following univariate analyses, we ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5647049</comments>
            <pubDate>Wed, 25 Jan 2012 18:04:45 +0100</pubDate>
            <guid isPermaLink="false">5647049</guid>        </item>
        <item>
            <title>Are viruses associated with human breast cancer? Scrutinizing the molecular evidence</title>
            <link>http://www.medworm.com/index.php?rid=5638087&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Flt837m7370271446%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The three viruses most studied as possible causes of human breast cancer are mouse mammary tumor virus-like sequences (MMTV-LS),
 Epstein-Barr virus (EBV), and oncogenic (high risk) types of human papilloma virus (HPV). The first step in fulfilling traditional
 criteria for inferring that a cancer is caused by a virus is to demonstrate the virus in the affected tissue. Molecular techniques,
 compared to host antibody assessment and immunohistochemistry, are the most definitive in establishing viral presence. Results
 of 85 original molecular research investigations to detect one or more of the three viruses have been extremely divergent
 with no consensus reached. We evaluated the methodology of these studies for the following: type of molecular assay, DNA/RNA
 quality ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638087</comments>
            <pubDate>Tue, 24 Jan 2012 18:09:20 +0100</pubDate>
            <guid isPermaLink="false">5638087</guid>        </item>
        <item>
            <title>Structural/organizational characteristics of health services partly explain racial variation in timeliness of radiation therapy among elderly breast cancer patients</title>
            <link>http://www.medworm.com/index.php?rid=5638088&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0t76238402435066%2F</link>
            <description>We examined the role of surgical facility characteristics and distance to care in
 explaining racial/ethnic variation in timing of initiation of guideline-recommended radiation therapy (RT) after breast conserving
 surgery (BCS). We used Surveillance Epidemiology and End Results-Medicare data to identify women ages 65 and older diagnosed
 with stages I–III breast cancer and treated with BCS in 1994–2002. We used stepwise multivariate logistic regression to examine
 the interactive effects of race/ethnicity and facility profit status, teaching status, size, and institutional affiliations,
 and distance to nearest RT on timing of RT initiation, controlling for known covariates. Among 38,574 eligible women who received
 BCS, 39% received RT within 2&amp;nbsp;months, 52% received RT within 6&amp;n...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638088</comments>
            <pubDate>Tue, 24 Jan 2012 07:35:09 +0100</pubDate>
            <guid isPermaLink="false">5638088</guid>        </item>
        <item>
            <title>Overexpression of a novel cell cycle regulator ecdysoneless in breast cancer: a marker of poor prognosis in HER2/neu-overexpressing breast cancer patients</title>
            <link>http://www.medworm.com/index.php?rid=5638091&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx875067w28067748%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Uncontrolled proliferation is one of the hallmarks of breast cancer. We have previously identified the human Ecd protein (human
 ortholog of Drosophila Ecdysoneless, hereafter called Ecd) as a novel promoter of mammalian cell cycle progression, a function related to its ability to remove
 the repressive effects of Rb-family tumor suppressors on E2F transcription factors. Given the frequent dysregulation of cell
 cycle regulatory components in human cancer, we used immunohistochemistry of paraffin-embedded tissues to examine Ecd expression
 in normal breast tissue versus tissues representing increasing breast cancer progression. Initial studies of a smaller cohort
 without outcomes information showed that Ecd expression was barely detectable in normal breast tissue and i...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638091</comments>
            <pubDate>Tue, 24 Jan 2012 07:35:08 +0100</pubDate>
            <guid isPermaLink="false">5638091</guid>        </item>
        <item>
            <title>Prognostic impact of placenta growth factor and vascular endothelial growth factor A in patients with breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5638090&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ffk07458834rr1545%2F</link>
            <description>In conclusion, our results
 support the mutual relationship between PlGF and VEGF-A and encourage further investigations as prognostic markers in breast
 cancer patients.
 
 
	Content Type Journal ArticleCategory Clinical TrialPages 1-9DOI 10.1007/s10549-012-1957-0Authors
		Else Maae, Department of Oncology, Vejle Hospital, Kabbeltoft 25, 7100 Vejle, DenmarkDorte Aalund Olsen, Department of Clinical Biochemistry, Vejle Hospital, Kabbeltoft 25, 7100 Vejle, DenmarkKarina Dahl Steffensen, Department of Oncology, Vejle Hospital, Kabbeltoft 25, 7100 Vejle, DenmarkErik Hugger Jakobsen, Department of Oncology, Vejle Hospital, Kabbeltoft 25, 7100 Vejle, DenmarkIvan Brandslund, Department of Clinical Biochemistry, Vejle Hospital, Kabbeltoft 25, 7100 Vejle, DenmarkFlemming Brandt Sørensen, Departme...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638090</comments>
            <pubDate>Tue, 24 Jan 2012 07:35:08 +0100</pubDate>
            <guid isPermaLink="false">5638090</guid>        </item>
        <item>
            <title>Prospective study of breast tomosynthesis as a triage to assessment in screening</title>
            <link>http://www.medworm.com/index.php?rid=5638089&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fpn275611n2757806%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;There is limited evidence on the role of 3D mammography with tomosynthesis in breast screening, although early studies suggest
 that it may improve specificity. We prospectively evaluated the effect of integrating 3D mammography as a triage to assessment
 in 158 consecutive recalls to assessment (recalled in standard 2D-mammographic screening) in asymptomatic subjects. Radiologists
 provided 3D mammography-based opinion as to whether recall/assessment was warranted or unnecessary, and all subjects proceeded
 to assessment. 3D triage was positive (confirmed the need for assessment) in all 21 subjects with breast cancer (there were
 no false negatives), and would have avoided recall in 102 of 137 (74.4%) subjects with a negative/benign final outcome in whom 3D triage did ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638089</comments>
            <pubDate>Tue, 24 Jan 2012 07:35:08 +0100</pubDate>
            <guid isPermaLink="false">5638089</guid>        </item>
        <item>
            <title>Stromal–epithelial interactions modulate cross-talk between prolactin receptor and HER2/Neu in breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5638092&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fnp126n71025802m4%2F</link>
            <description>In conclusion, CAFs play
 a critical role in bridging the cross-talk between PRL and HER2/Neu in both mouse and human models of breast cancer. The inhibitory
 effects of G129R on p-Neu and on tumor growth are dependent upon interactions of tumor epithelial cells with CAFs.
 
 
	Content Type Journal ArticleCategory Preclinical studyPages 1-13DOI 10.1007/s10549-012-1954-3Authors
		Cong Xu, Department of Biological Sciences, Clemson University, Clemson, SC 29634, USAJohn F. Langenheim, Department of Biological Sciences, Clemson University, Clemson, SC 29634, USAWen Y. Chen, Department of Biological Sciences, Clemson University, Clemson, SC 29634, USA
	

	
		Journal Breast Cancer Research and TreatmentOnline ISSN 1573-7217Print ISSN 0167-6806 (Source: Breast Cancer Research and Treatment)</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638092</comments>
            <pubDate>Tue, 24 Jan 2012 07:35:07 +0100</pubDate>
            <guid isPermaLink="false">5638092</guid>        </item>
        <item>
            <title>Autologous microsurgical breast reconstruction and coronary artery bypass grafting: an anatomical study and clinical implications</title>
            <link>http://www.medworm.com/index.php?rid=5638093&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6433572544511574%2F</link>
            <description>Conclusion We outline five methods of preserving the IMA for future CABG: (1) lowering the level of DIEP flaps to the fourth- and fifth-intercostals
 spaces, (2) using the DIEP pedicle as an intermediary for CABG, (3) using IMA perforators to spare the IMA proper, (4) using
 and end-to-side anastomosis between the DIEP pedicle and IMA and (5) anastomosis of DIEP flaps using retrograde flow from
 the distal IMA. With careful patient selection, we hypothesize using the IMA for autologous breast reconstruction need not
 be an absolute contraindication for future CABG.
 
 
	Content Type Journal ArticleCategory Preclinical StudyPages 1-18DOI 10.1007/s10549-011-1948-6Authors
		Warren M. Rozen, Jack Brockhoff Reconstructive Plastic Surgery Research Unit, Department of Anatomy and Cell Biology, Un...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638093</comments>
            <pubDate>Tue, 24 Jan 2012 07:35:05 +0100</pubDate>
            <guid isPermaLink="false">5638093</guid>        </item>
        <item>
            <title>Incidence of reduced chemotherapy relative dose intensity among women with early stage breast cancer in US clinical practice</title>
            <link>http://www.medworm.com/index.php?rid=5638096&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl038nq22r8v64453%2F</link>
            <description>This study employed a retrospective cohort design and electronic medical records from &amp;gt;65 community oncology/hematology
 clinics in &amp;gt;35 states (2004–2010). The study population comprised adult women who received myelosuppressive chemotherapy for
 ESBC (stages I–IIIA). For each such woman, each unique cycle of chemotherapy within their first observed course was identified.
 Incidence of chemotherapy dose delays (≥7&amp;nbsp;days for any drug in ≥1 cycles), chemotherapy dose reductions (≥15% for any drug
 in ≥1 cycles), and low chemotherapy relative dose intensity (RDI &amp;lt;85% over the course) relative to published reference standards
 were descriptively analyzed for the seven most-frequently planned regimens in the study database. A total of 2,228 women (70%
 of the subjects w...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638096</comments>
            <pubDate>Tue, 24 Jan 2012 07:35:04 +0100</pubDate>
            <guid isPermaLink="false">5638096</guid>        </item>
        <item>
            <title>Small node-negative (T1b-cN0) invasive hormone receptor-positive breast cancers: Is there a subpopulation that might have benefit from adjuvant chemotherapy?</title>
            <link>http://www.medworm.com/index.php?rid=5638095&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fvk42248503k7xt41%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aims of the study were to identify a subpopulation more likely to be at greater risk of recurrence in small T1b-c node-negative
 hormone receptor (HR)-positive breast cancer, and which would benefit from adjuvant chemotherapy. Clinico-pathologic characteristics
 and clinical outcomes of 538 postoperative HR-positive T1b-cN0 breast cancer patients were retrospectively analyzed. High
 Ki67 index and a young age (&amp;lt;35&amp;nbsp;years) were identified as independent risk factors for relapse (p&amp;nbsp;&amp;lt;&amp;nbsp;0.0001 and 0.015, respectively). A nomogram based on Cox-regression model showed an area under the curve (AUC) of 0.73
 in the training set. The validation set showed a good discrimination with an AUC of 0.65. In patients with high nomogram scores
 (≥100, n&amp;nbsp;=&amp;nb...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638095</comments>
            <pubDate>Tue, 24 Jan 2012 07:35:04 +0100</pubDate>
            <guid isPermaLink="false">5638095</guid>        </item>
        <item>
            <title>Assessing the added value of breast tumor markers in genetic risk prediction model BRCAPRO</title>
            <link>http://www.medworm.com/index.php?rid=5638094&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd406728324842206%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp; The BRCAPRO model estimates carrier probabilities for the BRCA1 and BRCA2 genes, and was recently enhanced to use estrogen
 receptor (ER) and progesterone receptor (PR) status of breast cancer. No independent assessment of the added value of these
 markers exists. Moreover, earlier versions of BRCAPRO did not use human epidermal growth factor receptor 2 (Her-2/neu) status
 of breast cancer. Here, we incorporate Her-2/neu in BRCAPRO and validate all the markers. We trained the enhanced model on
 406 germline tested individuals, and validated on a separate clinical cohort of 796 individuals for whom test results and
 family history are available. For model-building, we estimated joint probabilities of ER, PR, and Her-2/neu status for carriers
 and non-carriers of BRCA1/2...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638094</comments>
            <pubDate>Tue, 24 Jan 2012 07:35:04 +0100</pubDate>
            <guid isPermaLink="false">5638094</guid>        </item>
        <item>
            <title>Ipsilateral hemodialysis access after axillary dissection for breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5638097&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk8k1461u1k61l125%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Breast cancer survivors who have had axillary lymph node dissection (ALND) and who later develop end-stage renal failure may
 eventually require hemodialysis access. If veins available for access in the contralateral arm have been exhausted, especially
 after chemotherapy, the ipsilateral arm will have to be considered for access construction. There are no evidence-based guidelines
 for lymphedema prevention, but there are sweeping recommendations to avoid physical injury to the ipsilateral limb, including
 needle puncture, after ALND with or without radiotherapy. Three studies have shown little or no effect of hand surgery in
 producing or exacerbating lymphedema after ALND. Dialysis access guidelines recommend the use of autogenous accesses over
 synthetic grafts when...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638097</comments>
            <pubDate>Tue, 24 Jan 2012 07:35:03 +0100</pubDate>
            <guid isPermaLink="false">5638097</guid>        </item>
        <item>
            <title>Docetaxel-containing adjuvant chemotherapy in patients with early stage breast cancer. Consistency of effect independent of nodal and biomarker status: a meta-analysis of 14 randomized clinical trials</title>
            <link>http://www.medworm.com/index.php?rid=5638098&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbu57h47164013270%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The benefit of taxanes in the adjuvant setting for node-negative (N0) early breast cancer (EBC) has not yet been established.
 We conducted a meta-analysis of randomized adjuvant trials comparing docetaxel-containing versus non-taxane-containing regimens.
 The purpose of this study was to determine whether the incorporation of docetaxel improves disease-free survival (DFS) and
 overall survival (OS) in early stage breast cancer. Studies were retrieved by searching major databases and the proceedings
 of leading breast cancer conferences. We extracted hazard ratios (HRs) and 95% confidence intervals (CIs) for DFS and OS and
 obtained pooled estimates using an inverse-variance model. Fourteen randomized phase III studies were included (25,067 patients).
 The pooled HR est...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638098</comments>
            <pubDate>Tue, 24 Jan 2012 07:35:02 +0100</pubDate>
            <guid isPermaLink="false">5638098</guid>        </item>
        <item>
            <title>Mechanistic analysis of the antitumor efficacy of human natural killer cells against breast cancer cells</title>
            <link>http://www.medworm.com/index.php?rid=5619692&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv04275p79710v7m7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We investigated the role of human natural killer (NK) cells in the peripheral blood (PB) and liver in controlling breast cancer.
 The proportion of NK cells among liver mononuclear cells was significantly higher than among PB mononuclear cells. Liver NK
 cells inductively expressed higher levels of tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) than PB NK cells
 in response to interleukin-2 (IL-2). Liver NK cells displayed higher cytotoxicity against various breast cancer cell lines
 (MDA-MB231, MDA-MB453, MDA-MB468, and MCF-7) after IL-2 stimulation than did PB NK cells. Anti-HER2 monoclonal antibody (mAb)
 promoted the cytotoxicity of both the types of NK cells toward HER2-expressing cell lines. All breast cancer cell lines highly
 expressed death-ind...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5619692</comments>
            <pubDate>Fri, 20 Jan 2012 07:04:07 +0100</pubDate>
            <guid isPermaLink="false">5619692</guid>        </item>
        <item>
            <title>Phase II trial of temsirolimus in patients with metastatic breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5596960&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Frm656m8773014558%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Preclinical models suggested that activating mutations of the PIK3CA gene are associated with sensitivity to inhibitors of the mammalian target of rapamycin (mTOR). In breast cancers, PIK3CA mutations are associated with estrogen receptor (ER) positivity. We therefore performed an open-label single arm phase II
 study of the rapamycin analog, temsirolimus, at a dose of 25&amp;nbsp;mg weekly, in women with pretreated breast cancers that were
 positive for ER, PR, or HER2. Archived formalin-fixed paraffin embedded tumor was collected for immunohistochemical evaluation
 of components of the PI3K/Akt/mTOR pathway and PIK3CA mutation analysis. Thirty-one patients were enrolled. There were no major objective responses; however, three patients had
 stable disease for over 24&amp;nbsp;...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5596960</comments>
            <pubDate>Fri, 13 Jan 2012 16:57:39 +0100</pubDate>
            <guid isPermaLink="false">5596960</guid>        </item>
        <item>
            <title>Long-term follow-up of Jewish women with a BRCA1 and BRCA2 mutation who underwent population genetic screening</title>
            <link>http://www.medworm.com/index.php?rid=5596961&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk3t2341958131w5m%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;There are two mutations in BRCA1 and one in BRCA2, which are present in up to 2.5% of Jewish women. Population genetic testing
 for Jewish women has been proposed; however, it is unclear how this would impact the uptake of cancer prevention options and
 psychosocial functioning in women with a positive result. Two thousand and eighty unselected Jewish women were tested for
 the Jewish BRCA mutations, and 1.1% were positive. Cancer-related distress was measured before testing, and at 1 and 2&amp;nbsp;years
 post-testing. Information on uptake of cancer risk reduction options was collected at 2&amp;nbsp;years. Breast and ovarian cancer risks
 were estimated using BRCAPRO. Within 2&amp;nbsp;years of receiving a positive result, 11.1% of women had prophylactic mastectomy, and
 89.5% ha...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5596961</comments>
            <pubDate>Thu, 12 Jan 2012 16:49:06 +0100</pubDate>
            <guid isPermaLink="false">5596961</guid>        </item>
        <item>
            <title>Melatonin suppresses aromatase expression and activity in breast cancer associated fibroblasts</title>
            <link>http://www.medworm.com/index.php?rid=5596962&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe67024068703686h%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The main biological active substance secreted by the pineal gland, melatonin (MLT), counteracts the effects of estrogens in
 breast cancer via exerting a number of its own oncostatic properties. Recent studies of postmenopausal women have identified
 that the major metabolite of MLT is statistically significantly associated with a lower risk of developing breast cancer.
 While MLT production decreases with age, breast cancer risk, however, increases with age and obesity. We hypothesize that
 MLT inhibits estrogen production in breast adipose fibroblasts (BAFs), the main local source of estrogen in breast tumors
 of postmenopausal women, by inhibiting transcription of the CYP19A1 gene that encodes the key enzyme aromatase. Normal BAFs were cultured from women undergoing ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5596962</comments>
            <pubDate>Wed, 11 Jan 2012 17:56:47 +0100</pubDate>
            <guid isPermaLink="false">5596962</guid>        </item>
        <item>
            <title>Health-related quality of life, psychological distress, and adverse events in postmenopausal women with breast cancer who receive tamoxifen, exemestane, or anastrozole as adjuvant endocrine therapy: National Surgical Adjuvant Study of Breast Cancer 04 (N-SAS BC 04)</title>
            <link>http://www.medworm.com/index.php?rid=5596964&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F72n6435042104m8k%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Health-related quality of life (HRQOL), symptoms of depression, and adverse events (AEs) were compared between Japanese postmenopausal
 patients with hormone-sensitive breast cancer (BC) who received adjuvant tamoxifen, exemestane, or anastrozole in an open-labeled,
 randomized, multicenter trial designated as the National Surgical Adjuvant Study of Breast Cancer (N-SAS BC) 04 substudy of
 the Tamoxifen Exemestane Adjuvant Multinational (TEAM) trial. During the first year of treatment, HRQOL and symptoms of depression
 were analyzed using the Functional Assessment of Cancer Therapy-Breast (FACT-B) and its Endocrine Symptom Subscale (ES), and
 the Center for Epidemiologic Studies Depression Scale (CES-D), respectively. In addition, predefined AEs were analyzed. A
 total ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5596964</comments>
            <pubDate>Tue, 10 Jan 2012 16:49:30 +0100</pubDate>
            <guid isPermaLink="false">5596964</guid>        </item>
        <item>
            <title>Molecular insights on basal-like breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5596963&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7q80334311kj9hx2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Molecular classification of breast cancer (BC) identified diverse subgroups that encompass distinct biological behavior and
 clinical implications, in particular in relation to prognosis, spread, and incidence of recurrence. Basal-like breast cancers
 (BLBC) compose up to 15% of BC and are characterized by lack of estrogen receptor (ER), progesterone receptor (PR), and HER-2
 amplification with expression of basal cytokeratins 5/6, 14, 17, epidermal growth factor receptor (EGFR), and/or c-KIT. There
 is an overlap in definition between triple-negative BC and BLBC due to the triple-negative profile of BLBC. Also, most BRCA1-associated
 BCs are BLBC, triple negative, and express basal cytokeratins (5/6, 14, 17) and EGFR. There is a link between sporadic BLBC
 (occurring i...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5596963</comments>
            <pubDate>Tue, 10 Jan 2012 16:49:30 +0100</pubDate>
            <guid isPermaLink="false">5596963</guid>        </item>
        <item>
            <title>Higher expression of androgen receptor is a significant predictor for better endocrine-responsiveness in estrogen receptor-positive breast cancers</title>
            <link>http://www.medworm.com/index.php?rid=5596965&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr63p6g7567982614%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim was to investigate the implications of androgen receptor (AR) expression levels on outcomes for estrogen receptor
 (ER)-positive tumors. Immunohistochemically AR levels were determined from tissue microarrays of 614 ER-positive patients
 who received adjuvant endocrine with or without chemotherapy between November 1999 and August 2005. Characteristics and survival
 were analyzed using a Chi-square test, Kaplan–Meier methods, and Cox’s models. AR levels were categorized into 3 subgroups
 as follows: low, AR&amp;nbsp;&amp;lt;&amp;nbsp;10%; intermediate, 10%&amp;nbsp;≤&amp;nbsp;AR&amp;nbsp;&amp;lt;&amp;nbsp;50%; high, AR&amp;nbsp;≥&amp;nbsp;50%. Low, intermediate, and high AR levels were observed
 in 29.0, 44.0, and 27.0% of patients, respectively. High AR was associated with smaller size, nodal ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5596965</comments>
            <pubDate>Mon, 09 Jan 2012 19:38:26 +0100</pubDate>
            <guid isPermaLink="false">5596965</guid>        </item>
        <item>
            <title>Molecular and clinical characterization of an in frame deletion of uncertain clinical significance in the BRCA2 gene</title>
            <link>http://www.medworm.com/index.php?rid=5581005&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6240jl2128333m20%2F</link>
            <description>In this study, we analyzed a “variant of uncertain significance” (VUS) located in exon 23 of the BRCA2 gene exhibited by six members of five distinct families with hereditary breast cancer (BC). The variant was identified by
 DNA sequencing, and cDNA analysis revealed its co-expression with wild-type mRNA. We analyzed co-occurrence with other pathological
 mutations in BRCA1/2, performed a case–control study, looked for evolutionary data and used in-silico analyses to predict its potential clinical
 significance. Sequencing revealed an in frame deletion of 126 nucleotides in exon 23, leading to a deletion of 42 amino acids
 (c.9203_9328del126, p.Pro2992_Thr3033del). All of the VUS-carriers suffered from either BC or ovarian/pancreatic cancer. No
 other definite pathologic mutation of...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5581005</comments>
            <pubDate>Sat, 07 Jan 2012 16:51:25 +0100</pubDate>
            <guid isPermaLink="false">5581005</guid>        </item>
        <item>
            <title>Methylation of O6-methylguanine-DNA methyltransferase (MGMT) promoter gene in triple-negative breast cancer patients</title>
            <link>http://www.medworm.com/index.php?rid=5581004&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fek8361mx12477650%2F</link>
            <description>In conclusion, our data suggest that in TNBC
 with wild-type BRCA1, the direct DNA repair system may be frequently (63.6%) silenced by MGMT methylation. The evaluation
 of the MGMT status could offer a new adjunct in predicting tumor response to alkylating drugs in TNBC patients.
 
 
	Content Type Journal ArticleCategory Preclinical StudyPages 1-7DOI 10.1007/s10549-011-1945-9Authors
		Caterina Fumagalli, Division of Pathology, European Institute of Oncology, Via Ripamonti 435, 20141 Milan, ItalyGiancarlo Pruneri, Division of Pathology, European Institute of Oncology, Via Ripamonti 435, 20141 Milan, ItalyPaola Possanzini, Division of Pathology, European Institute of Oncology, Via Ripamonti 435, 20141 Milan, ItalyMichela Manzotti, Division of Pathology, European Institute of Oncology, Via Ri...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5581004</comments>
            <pubDate>Sat, 07 Jan 2012 16:51:25 +0100</pubDate>
            <guid isPermaLink="false">5581004</guid>        </item>
        <item>
            <title>Zosuquidar and an albumin-binding prodrug of zosuquidar reverse multidrug resistance in breast cancer cells of doxorubicin and an albumin-binding prodrug of doxorubicin</title>
            <link>http://www.medworm.com/index.php?rid=5581006&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2p5u73m52r22r464%2F</link>
            <description>In this study, we consequently developed an acid-sensitive albumin-binding
 prodrug of the P-gp inhibitor zosuquidar (LY335979) in a two-step synthesis using a maleimide hydrazone linker system established
 in our laboratory that first introduces acetylbenzoic acid at the HO-group of zosuquidar followed by derivatization with 6-maleimidocaproyl
 hydrazide to form the acid-sensitive hydrazone bond. The maleimide group enables the prodrug to bind rapidly and selectively
 to the cysteine-34 position of endogenous albumin after intravenous administration. HPLC analysis demonstrated rapid albumin
 binding of the zosuquidar prodrug as well as the quantitative release of the acetylbenzoic ester derivative of zosuquidar
 at pH 5.0. Subsequently, its ability to circumvent MDR was tested in two doxo...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5581006</comments>
            <pubDate>Sat, 07 Jan 2012 06:44:09 +0100</pubDate>
            <guid isPermaLink="false">5581006</guid>        </item>
        <item>
            <title>Mammographic density, parity and age at first birth, and risk of breast cancer: an analysis of four case–control studies</title>
            <link>http://www.medworm.com/index.php?rid=5581007&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc44t535p130t644u%2F</link>
            <description>In conclusion, this study did not support the hypothesis that parity modifies the breast cancer risk attributed to mammographic
 density. Even though an effect modification was found in Hawaiian women, no such thing was found in women from the other three
 locations.
 
 
	Content Type Journal ArticleCategory EpidemiologyPages 1-9DOI 10.1007/s10549-011-1929-9Authors
		Christy G. Woolcott, Departments of Obstetrics &amp; Gynaecology and Pediatrics, Dalhousie University, Halifax, NS, CanadaKarin Koga, University of Hawaii Cancer Center, Honolulu, HI, USAShannon M. Conroy, University of Hawaii Cancer Center, Honolulu, HI, USACelia Byrne, Georgetown Lombardi Comprehensive Cancer Center, Washington, DC, USAChisato Nagata, Gifu University Graduate School of Medicine, Gifu, JapanGiske Ursin, Universit...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5581007</comments>
            <pubDate>Thu, 05 Jan 2012 17:05:06 +0100</pubDate>
            <guid isPermaLink="false">5581007</guid>        </item>
        <item>
            <title>A dietary pattern derived to correlate with estrogens and risk of postmenopausal breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5581008&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd62vj21w26x2w345%2F</link>
            <description>In conclusion, diet pattern
 appeared to only have modest association with estrogens, and was not associated with postmenopausal breast cancer risk. Although
 these results were null, it should be repeated in other populations as differences in food intake may yield a dietary pattern
 with stronger association with estrogens.
 
 
	Content Type Journal ArticleCategory EpidemiologyPages 1-6DOI 10.1007/s10549-011-1942-zAuthors
		Teresa T. Fung, Department of Nutrition, Simmons College, 300 The Fenway, Boston, MA 02115, USAMatthias B. Schulze, Department of Molecular Epidemiology, German Institute of Nutrition, Potsdam, Arthur-Scheunert-Allee 114-116, 14558 Nuthetal, GermanyFrank B. Hu, Department of Nutrition, Harvard School of Public Health, 677 Huntington Ave, Boston, MA 02115, USASusan E. ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5581008</comments>
            <pubDate>Thu, 05 Jan 2012 06:51:44 +0100</pubDate>
            <guid isPermaLink="false">5581008</guid>        </item>
        <item>
            <title>US follow-up protocol in concordant benign result after US-guided 14-gauge core needle breast biopsy</title>
            <link>http://www.medworm.com/index.php?rid=5571963&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1w6001611x042484%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To determine the time when follow-up ultrasound (US) should begin for concordant benign lesions after US-guided 14-gauge core
 needle breast biopsy (CNB). This was an IRB–approved retrospective study, with a waiver of informed consent. Among 3,888 consecutive
 US-guided CNBs performed between August 2005 and March 2008, 1,492 breast masses in 1,309 women with concordant benign results
 and follow-up US after CNB were included. Their medical records were reviewed. Statistical comparisons for the result of first
 follow-up US and malignant rates among 6-month, 12-month, and long-term intervals were performed by using Fisher exact test.
 Results dichotomized for symptom, lesion size (10&amp;nbsp;mm), and CNB result (specific or not), were also analyzed. In 1,492 masses,
 sev...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5571963</comments>
            <pubDate>Wed, 04 Jan 2012 17:02:24 +0100</pubDate>
            <guid isPermaLink="false">5571963</guid>        </item>
        <item>
            <title>Gamma-ray-induced mutagen sensitivity and risk of sporadic breast cancer in young women: a case–control study</title>
            <link>http://www.medworm.com/index.php?rid=5571964&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq518458471071m7m%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Hypersensitivity to radiation exposure has been suggested to be a risk factor for the development of breast cancer. In this
 case–control study of 515 young women (≤55&amp;nbsp;years) with newly diagnosed sporadic breast cancer and 402 cancer-free controls,
 we examined the radiosensitivity as measured by the frequency of chromatid breaks induced by gamma-radiation exposure in the
 G2 phase of phytohemagglutinin-stimulated and short-term cultured fresh lymphocytes. We found that the average chromatid breaks
 per cell from 50 well-spread metaphases were statistically significantly higher in 403 non-Hispanic White breast cancer patients
 (0.52&amp;nbsp;±&amp;nbsp;0.22) than that in 281 non-Hispanic White controls (0.44&amp;nbsp;±&amp;nbsp;0.16) (P value&amp;nbsp;&amp;lt;&amp;nbsp;0.001), and in 60...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5571964</comments>
            <pubDate>Wed, 04 Jan 2012 17:02:23 +0100</pubDate>
            <guid isPermaLink="false">5571964</guid>        </item>
        <item>
            <title>Obstetric history and mammographic density: a population-based cross-sectional study in Spain (DDM-Spain)</title>
            <link>http://www.medworm.com/index.php?rid=5571966&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk6871118706461uv%2F</link>
            <description>This study
 investigates the influence of obstetric factors on MD among pre- and post-menopausal women. We enrolled 3,574 women aged 45–68&amp;nbsp;years
 who were participating in breast cancer screening programmes in seven screening centers. To measure MD, blind anonymous readings
 were taken by an experienced radiologist, using craniocaudal mammography and Boyd’s semiquantitative scale. Demographic and
 reproductive data were directly surveyed by purpose-trained staff at the date of screening. The association between MD and
 obstetric variables was quantified by ordinal logistic regression, with screening centre introduced as a random effect term.
 We adjusted for age, number of children and body mass index, and stratified by menopausal status. Parity was inversely associated
 with dens...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5571966</comments>
            <pubDate>Wed, 04 Jan 2012 06:46:38 +0100</pubDate>
            <guid isPermaLink="false">5571966</guid>        </item>
        <item>
            <title>Fruit and vegetables consumption and breast cancer risk: the EPIC Italy study</title>
            <link>http://www.medworm.com/index.php?rid=5571965&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu5t18610064r8789%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The role of fruit and vegetables in breast cancer (BC) development has long been debated. A large variety of vegetables and
 fruit are consumed by Mediterranean populations, a favourable setting for evaluating the effects of these foods. The association
 between vegetables and fruit consumption, overall and by specific types, and BC risk was studied in the Italian section of
 the European Prospective Investigation into Cancer and Nutrition study. Over 31,000 women, aged 36-64&amp;nbsp;years, recruited in
 five Italian centers between 1993 and 1998, were available for analyses with dietary and lifestyle information and anthropometric
 measurements. After a median follow-up of 11.25&amp;nbsp;years, 1,072 invasive and in situ incident BC cases were identified. Cox proportional
 ha...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5571965</comments>
            <pubDate>Wed, 04 Jan 2012 06:46:38 +0100</pubDate>
            <guid isPermaLink="false">5571965</guid>        </item>
        <item>
            <title>The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriers</title>
            <link>http://www.medworm.com/index.php?rid=5571967&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6tr4w243q1vkhj02%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 Klotho (KL) is a putative tumor suppressor gene in breast and pancreatic cancers located at chromosome 13q12. A functional sequence
 variant of Klotho (KL-VS) was previously reported to modify breast cancer risk in Jewish BRCA1 mutation carriers. The effect of this variant on breast and ovarian cancer risks in non-Jewish BRCA1/BRCA2 mutation carriers has not been reported. The KL-VS variant was genotyped in women of European ancestry carrying a BRCA mutation: 5,741 BRCA1 mutation carriers (2,997 with breast cancer, 705 with ovarian cancer, and 2,039 cancer free women) and 3,339 BRCA2 mutation carriers (1,846 with breast cancer, 207 with ovarian cancer, and 1,286 cancer free women) from 16 centers. Genotyping
 was accomplished using TaqMan® allelic discrimination or m...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5571967</comments>
            <pubDate>Mon, 02 Jan 2012 16:49:44 +0100</pubDate>
            <guid isPermaLink="false">5571967</guid>        </item>
        <item>
            <title>SLC22A5/OCTN2 expression in breast cancer is induced by estrogen via a novel intronic estrogen-response element (ERE)</title>
            <link>http://www.medworm.com/index.php?rid=5571968&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw1881n71832ur0j7%2F</link>
            <description>In this study,
 we found that estrogen stimulates SLC22A5 expression robustly in an estrogen receptor (ER)-dependent manner and that SLC22A5
 expression is associated with ER status in breast cancer cell lines and tissue specimens. Although the SLC22A5 proximal promoter
 is not responsive to estrogen, a downstream intronic enhancer confers estrogen inducibility. This intronic enhancer contains
 a newly identified estrogen-responsive element (ERE) (GGTCA-CTG-TGACT) and other transcription factor binding sites, such
 as a half ERE and a nuclear receptor related 1 (NR4A2/Nurr1) site. Estrogen induction of the luciferase reporter was dependent
 upon both the ERE and the NR4A2 site within the intronic enhancer. Small interfering RNA against either ER or Nurr1 inhibited
 estrogen induction of SL...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5571968</comments>
            <pubDate>Mon, 02 Jan 2012 16:49:43 +0100</pubDate>
            <guid isPermaLink="false">5571968</guid>        </item>
        <item>
            <title>Primary and secondary angiosarcomas of the breast: a single institution experience</title>
            <link>http://www.medworm.com/index.php?rid=5559438&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F163nkh477377hp0n%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Angiosarcomas of the breast (ASB) are rare, representing &amp;lt;1% of breast malignancies. They can develop as a primary or secondary
 malignancy, also called post-radiation angiosarcoma. The aim of the this study is to discuss diagnosis, treatment, and outcome
 of primary and secondary ASB patients, diagnosed and treated in a single institution, over a 10-year period and to further
 compare the two conditions. We retrieved 28 consecutive cases of ASB, diagnosed from 1999 to 2009 at the European Institute
 of Oncology. Clinical and pathologic findings and survival analyses were performed. Of the 28 cases (27 women and 1 man),
 eight were primary breast angiosarcomas (PBA) and 20 were secondary breast angiosarcomas (SBA). Median follow-up was 23&amp;nbsp;months
 (range 1–112&amp;...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5559438</comments>
            <pubDate>Fri, 30 Dec 2011 07:08:45 +0100</pubDate>
            <guid isPermaLink="false">5559438</guid>        </item>
        <item>
            <title>Clinical and biomarker predictors of side effects from tamoxifen</title>
            <link>http://www.medworm.com/index.php?rid=5559439&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg8qq677xt234p621%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Tamoxifen decreases breast cancer recurrence, mortality, and breast cancer risk in high-risk women. Despite these proven benefits,
 tamoxifen use is often limited due to side effects. We identified predictors of tamoxifen-induced side effects based on clinical
 variables and serum tamoxifen metabolite biomarkers in a cross-sectional study of patients taking tamoxifen. We enrolled 241
 women and collected data on demographics, tamoxifen use and side effects, as well as potential clinical and serum predictors.
 We used logistic regression models and adjusted for age, body mass index, ethnicity, education, prior post-menopausal hormone
 therapy (HT), tamoxifen duration, and endoxifen levels to identify factors associated with side effects. Common tamoxifen
 attributed side...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5559439</comments>
            <pubDate>Fri, 30 Dec 2011 07:08:44 +0100</pubDate>
            <guid isPermaLink="false">5559439</guid>        </item>
        <item>
            <title>Global and focal brain volume in long-term breast cancer survivors exposed to adjuvant chemotherapy</title>
            <link>http://www.medworm.com/index.php?rid=5552035&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv00451777l542722%2F</link>
            <description>This study shows that adjuvant chemotherapy for breast cancer is associated with long-term reductions
 in TBV and overall gray matter volume in the absence of focal reductions. The observed smaller gray matter volume in chemotherapy-exposed
 survivors was comparable to the effect of almost 4&amp;nbsp;years of age on gray matter volume reduction. These volume differences
 might be associated with the slightly worse cognitive performance that we observed previously in this group of breast cancer
 survivors.
 
 
	Content Type Journal ArticleCategory EpidemiologyPages 1-8DOI 10.1007/s10549-011-1888-1Authors
		Vincent Koppelmans, Department of Epidemiology, Erasmus MC University Medical Center, Rotterdam, The NetherlandsMichiel B. de Ruiter, Department of Psychosocial Research and Epidemiology, Net...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552035</comments>
            <pubDate>Wed, 28 Dec 2011 16:51:15 +0100</pubDate>
            <guid isPermaLink="false">5552035</guid>        </item>
        <item>
            <title>Triple-negative breast cancer: the impact of guideline-adherent adjuvant treatment on survival—a retrospective multi-centre cohort study</title>
            <link>http://www.medworm.com/index.php?rid=5552034&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd5650451w4284p20%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Triple-negative breast cancer (TNBC) (ER−/PGR−/erb-2−) constitutes an aggressive subtype in breast cancer because it is accompanied
 by a significant decrease in overall survival (OAS) and recurrence-free survival (RFS) compared with hormone receptor positive
 breast cancers. This retrospective cohort study investigates the following issues: (1) Is there an impact of guideline-adherent
 treatment on RFS and OAS in TNBC? (2) Which adjuvant treatment has the most important impact on RFS and OAS in TNBC? This
 German retrospective multi-centre cohort study included 3,658 patients with primary breast cancer recruited from 2000 to 2005.
 The definition of guideline adherence was based on the German national S3 guideline for diagnosis and treatment of breast
 cancer (20...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552034</comments>
            <pubDate>Wed, 28 Dec 2011 16:51:15 +0100</pubDate>
            <guid isPermaLink="false">5552034</guid>        </item>
        <item>
            <title>Parity and mortality from causes other than breast cancer in breast cancer patients</title>
            <link>http://www.medworm.com/index.php?rid=5552037&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F94x57421j32343k1%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-5DOI 10.1007/s10549-011-1924-1Authors
		Mai Kadi, Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, St. Mary’s Campus, Norfolk Place, Paddington, London W2 1PG, UKPetra A. Wark, Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, St. Mary’s Campus, Norfolk Place, Paddington, London W2 1PG, UKMarc J. Gunter, Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, St. Mary’s Campus, Norfolk Place, Paddington, London W2 1PG, UKElio Riboli, Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, St. Mary’s Campus, Norfolk Place, Paddington, London W2 1P...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552037</comments>
            <pubDate>Tue, 27 Dec 2011 17:03:25 +0100</pubDate>
            <guid isPermaLink="false">5552037</guid>        </item>
        <item>
            <title>Biologically effective dose and breast cancer conservative treatment: is duration of radiation therapy really important?</title>
            <link>http://www.medworm.com/index.php?rid=5552036&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh52674141j203725%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To evaluate if biologically effective dose (BED), and in particular the duration of radiation treatment, has an effect on
 local relapse risk. Between January 2000 and December 2008 a total of 762 patients with T1-2 N0/+ breast cancer was treated
 with breast-conserving surgery and radiotherapy, with and without hormone therapy and chemotherapy. Adjuvant radiation therapy
 was administered to a total dose of 60–66&amp;nbsp;Gy in 30–33 fractions. The computed BEDs were divided in four groups: &amp;lt;43.1, 43.1–44.9,
 45.0–46.1, and &amp;gt;46.1&amp;nbsp;Gy (A–D, respectively). Kaplan–Meier method was used to calculate local relapse rates. Cox regression
 method was used to identify prognostic factors of local relapse. Evaluated variables were age, tumor histology, tumor siz...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552036</comments>
            <pubDate>Tue, 27 Dec 2011 17:03:25 +0100</pubDate>
            <guid isPermaLink="false">5552036</guid>        </item>
        <item>
            <title>Antitumor effects of cytoplasmic delivery of an innate adjuvant receptor ligand, poly(I:C), on human breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5552038&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg02m08116q7g04m1%2F</link>
            <description>In this study, we tested this possibility of using an innate adjuvant receptor ligand,
 polyinosinic–polycytidylic acid [poly(I:C)], to treat human breast cancer cell lines. Three breast cancer cell lines (MCF-7,
 MDA-MB-231, and BT-549) were used in this study. Poly(I:C) was transfected into these cancer cells to stimulate melanoma differentiation–associated
 gene (MDA) 5, which is a cytoplasmic adjuvant receptor. Poly(I:C) transfection significantly reduced the viability of all
 cell lines in a manner partially dependent on MDA5. Flow cytometeric analyses and immunoblot assays revealed that the antitumor
 effect depended on both caspase-dependent apoptosis and c-Myc- and cyclinD1-dependent growth arrest. Interestingly, poly(I:C)
 transfection was accompanied by autophagy, which is th...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552038</comments>
            <pubDate>Tue, 27 Dec 2011 17:03:23 +0100</pubDate>
            <guid isPermaLink="false">5552038</guid>        </item>
        <item>
            <title>A cost-benefit analysis of bevacizumab in combination with paclitaxel in the first-line treatment of patients with metastatic breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5552041&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8163613255857hq1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Bevacizumab in combination with chemotherapy increases progression-free survival (PFS), but not overall survival when compared
 to chemotherapy alone in the treatment of metastatic breast cancer (MBC). Recently in November, 2011 the Food and drug administration
 revoked approval of bevacizumab in combination with paclitaxel for the treatment of MBC. The European Medicines Agency, in
 contrast, maintained its approval of bevacizumab in MBC. While neither agency considers health economics in their decision-making
 process, one of the greatest challenges in oncology practice today is to reconcile hard-won small incremental clinical benefits
 with exponentially rising costs. To inform policy-makers in the US, this study aimed to assess the cost-effectiveness of bevacizumab/...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552041</comments>
            <pubDate>Mon, 26 Dec 2011 16:45:50 +0100</pubDate>
            <guid isPermaLink="false">5552041</guid>        </item>
        <item>
            <title>Phase I–II study of vorinostat plus paclitaxel and bevacizumab in metastatic breast cancer: evidence for vorinostat-induced tubulin acetylation and Hsp90 inhibition in vivo</title>
            <link>http://www.medworm.com/index.php?rid=5552040&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F951t60tw76k08162%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In preclinical models, the histone deacetylase inhibitor vorinostat sensitizes breast cancer cells to tubulin-polymerizing
 agents and to anti-vascular endothelial growth factor-directed therapies. We sought to determine the safety and efficacy of
 vorinostat plus paclitaxel and bevacizumab as first-line therapy in metastatic breast cancer (MBC), and the biological effects
 of vorinostat in vivo. For this purpose of this study, 54 patients with measurable disease and no prior chemotherapy for MBC
 received vorinostat (200 or 300&amp;nbsp;mg PO BID) on days 1–3, 8–10, and 15–17, plus paclitaxel (90&amp;nbsp;mg/m2) on days 2, 9, 16, and bevacizumab (10&amp;nbsp;mg/kg) on days 2 and 16 every 28&amp;nbsp;days. The primary objective of the phase I study
 was to determine the recommend...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552040</comments>
            <pubDate>Mon, 26 Dec 2011 16:45:50 +0100</pubDate>
            <guid isPermaLink="false">5552040</guid>        </item>
        <item>
            <title>Optimal outcomes for liver-dominant metastatic breast cancer with transarterial chemoembolization with drug-eluting beads loaded with doxorubicin</title>
            <link>http://www.medworm.com/index.php?rid=5552039&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr682837j7kg3r087%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The purpose of this study was to evaluate the efficacy of image-guided delivery of locoregional chemotherapy to breast cancer
 hepatic metastases using doxorubicin-loaded drug-eluting beads (DEBDOX). An IRB-approved multi-center, prospective, open,
 non-controlled repeat treatment registry to investigate the safety and efficacy of doxorubicin microspheres in the treatment
 of patients with unresectable liver metastasis from breast cancer was reviewed. Statistical analysis was performed with differences
 of P&amp;nbsp;&amp;lt;&amp;nbsp;0.05 considered significant. About 40 patients with metastatic breast cancer (MBC) to the liver underwent a total of 75
 image-guided procedures with hepatic arterial drug-eluting beads loaded with doxorubicin (DEBDOX). Treatment was well tolerated
 w...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5552039</comments>
            <pubDate>Mon, 26 Dec 2011 16:45:50 +0100</pubDate>
            <guid isPermaLink="false">5552039</guid>        </item>
        <item>
            <title>Genetic variants at chromosome 9p21, 10p15 and 10q22 and breast cancer susceptibility in a Chinese population</title>
            <link>http://www.medworm.com/index.php?rid=5544166&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkp408k55t42703x4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A recent genome-wide association study (GWAS) has identified a new subset of breast cancer susceptibility loci on chromosomes
 9, 10, and 11 in populations of European descent. However, because of the genetic heterogeneity, the role of these loci in
 non-European descent populations is still unclear. To evaluate the relationships between genetic variants in these regions
 identified by GWAS and breast cancer risk in Chinese women, we genotyped four common SNPs at 9p21(rs1011970 and rs10757278),
 10p15 (rs2380205), and 10q22 (rs1250009) in a two-stage case–control study with a total of 1792 breast cancer cases and 1,867
 controls. We found that rs1250009 at 10q22 was consistently associated with risk of breast cancer in stage 1 and stage 2,
 with a per-allele OR of 1.1...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544166</comments>
            <pubDate>Sat, 24 Dec 2011 16:42:13 +0100</pubDate>
            <guid isPermaLink="false">5544166</guid>        </item>
        <item>
            <title>Effect of baseline serum vitamin D levels on aromatase inhibitors induced musculoskeletal symptoms: results from the IBIS-II, chemoprevention study using anastrozole</title>
            <link>http://www.medworm.com/index.php?rid=5544167&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft2103212t7587330%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Severe deficiency of vitamin D in adults can cause musculoskeletal pain, stiffness, and joint discomfort. Musculoskeletal
 symptoms similar to those associated with vitamin D deficiency are frequently seen in breast cancer patients receiving adjuvant
 aromatase inhibitors (AIs). This is presumably due to oestrogen deficiency caused by AIs. However, no data are available on
 serum levels of vitamin D and their relation to developing musculoskeletal symptoms/arthralgia in women receiving an AI. IBIS-II
 is a multicentre randomized placebo controlled trial of the AI, anastrozole, in postmenopausal women aged 40–70&amp;nbsp;years, who
 are at increased risk of breast cancer. Serum vitamin D levels were measured for 416 participants. The samples were sent for
 assays in three ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544167</comments>
            <pubDate>Sat, 24 Dec 2011 16:42:12 +0100</pubDate>
            <guid isPermaLink="false">5544167</guid>        </item>
        <item>
            <title>Chemotherapy response and recurrence-free survival in neoadjuvant breast cancer depends on biomarker profiles: results from the I-SPY 1 TRIAL (CALGB 150007/150012; ACRIN 6657)</title>
            <link>http://www.medworm.com/index.php?rid=5544169&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh1j82416h86031k7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Neoadjuvant chemotherapy for breast cancer allows individual tumor response to be assessed depending on molecular subtype,
 and to judge the impact of response to therapy on recurrence-free survival (RFS). The multicenter I-SPY 1 TRIAL evaluated
 patients with ≥3&amp;nbsp;cm tumors by using early imaging and molecular signatures, with outcomes of pathologic complete response
 (pCR) and RFS. The current analysis was performed using data from patients who had molecular profiles and did not receive
 trastuzumab. The various molecular classifiers tested were highly correlated. Categorization of breast cancer by molecular
 signatures enhanced the ability of pCR to predict improvement in RFS compared to the population as a whole. In multivariate
 analysis, the molecular signatu...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544169</comments>
            <pubDate>Sat, 24 Dec 2011 16:42:11 +0100</pubDate>
            <guid isPermaLink="false">5544169</guid>        </item>
        <item>
            <title>Outcomes of a weight loss intervention among rural breast cancer survivors</title>
            <link>http://www.medworm.com/index.php?rid=5544168&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa8725q3x7nj6305k%2F</link>
            <description>In conclusion, the intervention produced &amp;gt;10% weight loss as well as significant improvements across multiple endpoints. The
 group phone-based treatment delivery approach may help disseminate effective weight control intervention to hard-to-reach
 breast cancer survivors.
 
 
	Content Type Journal ArticleCategory Clinical trialPages 1-9DOI 10.1007/s10549-011-1922-3Authors
		Christie A. Befort, Department of Preventive Medicine and Public Health, University of Kansas Medical Center, 3901 Rainbow Blvd, MS 1008, Kansas City, KS 66160, USAJennifer R. Klemp, Medical Oncology, Breast Cancer Prevention and Survivorship Center, University of Kansas Medical Center, Kansas City, KS, USAHeather L. Austin, Department of Preventive Medicine and Public Health, University of Kansas Medical Center, 39...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544168</comments>
            <pubDate>Sat, 24 Dec 2011 16:42:11 +0100</pubDate>
            <guid isPermaLink="false">5544168</guid>        </item>
        <item>
            <title>A phase II study of lapatinib and bevacizumab as treatment for HER2-overexpressing metastatic breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5544170&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8m46p22274m78832%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Preclinical data have demonstrated that the combination of antihuman epidermal growth factor receptor-2 (anti-HER2) and antivascular
 endothelial growth factor (anti-VEGF)—targeted agents has antitumor activity; these data indicate certain patients with HER2-overexpressing
 breast cancer may derive clinical benefit from this combination. The purpose of this single-arm phase II study was to determine
 the efficacy and safety of the dual-targeting combination of lapatinib and bevacizumab. Women with HER2-overexpressing advanced
 breast cancer received 1,500&amp;nbsp;mg oral lapatinib daily plus 10&amp;nbsp;mg/kg IV bevacizumab every 2&amp;nbsp;weeks. The primary endpoint was
 progression-free survival (PFS) at week 12; secondary endpoints included overall tumor response rate (ORR),...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544170</comments>
            <pubDate>Fri, 23 Dec 2011 16:52:50 +0100</pubDate>
            <guid isPermaLink="false">5544170</guid>        </item>
        <item>
            <title>Psoriasin (S100A7) increases the expression of ROS and VEGF and acts through RAGE to promote endothelial cell proliferation</title>
            <link>http://www.medworm.com/index.php?rid=5544172&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2jn774p781356v11%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Psoriasin (S100A7), originally identified in psoriasis, is a calcium-binding protein belonging to the multigenic S100 family.
 In high-grade ductal carcinoma in situ, psoriasin was identified as one of the most abundant transcripts. We have previously
 shown that psoriasin was induced by reactive oxygen species (ROS). Moreover, the downregulation of psoriasin by short hairpin
 RNA (shRNA) led to the reduced expression of vascular endothelial growth factor (VEGF) and inhibited tumor growth in vivo.
 The aim of the present study was to investigate whether psoriasin could have direct effects on endothelial cells. In this
 study we demonstrated that psoriasin increased VEGF expression in mammary epithelial cells. The treatment of endothelial cells
 with recombinant psoriasi...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544172</comments>
            <pubDate>Wed, 21 Dec 2011 20:04:56 +0100</pubDate>
            <guid isPermaLink="false">5544172</guid>        </item>
        <item>
            <title>Absence of ectopic epithelial inclusions in 3,904 axillary lymph nodes examined in sentinel technique</title>
            <link>http://www.medworm.com/index.php?rid=5544171&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj5229483761772vx%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Intraoperative examination of sentinel axillary lymph nodes can be done by imprint cytology, frozen section, or, most recently,
 by PCR-based amplification of a cytokeratin signal. Using this technique, benign epithelial inclusions, representing mammary
 tissue displaced along the milk line, will likely generate a positive PCR signal and lead to a false-positive diagnosis of
 metastatic disease. To better appreciate the incidence of ectopic epithelial inclusions in axillary lymph nodes, we have performed
 an autopsy study, examining on 100&amp;nbsp;μm step sections&amp;nbsp;3,904 lymph nodes obtained from 160 axillary dissections in 80 patients.
 The median number of lymph nodes per axilla was 23 (15, 6, and 1 in levels 1, 2, and 3, respectively). A total of 30,450 hematoxylin...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5544171</comments>
            <pubDate>Wed, 21 Dec 2011 20:04:56 +0100</pubDate>
            <guid isPermaLink="false">5544171</guid>        </item>
        <item>
            <title>Pre-diagnosis body mass index and survival after breast cancer in the After Breast Cancer Pooling Project</title>
            <link>http://www.medworm.com/index.php?rid=5537465&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu704m250177236q4%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Obese and underweight women who develop breast cancer may have poorer survival compared with normal-weight women. However,
 the optimal weight for best prognosis is still under study. We conducted a prospective investigation of pre-diagnosis body
 mass index (BMI) and mortality among 14,948 breast cancer patients in the After Breast Cancer Pooling Project. Breast cancer
 patients diagnosed from 1990 to 2006 with AJCC Stage I–III breast tumors were drawn from four prospective cohorts. Hazard
 ratios (HR) and 95% confidence intervals (CI) representing the associations of BMI categories (World Health Organization international
 classifications) with recurrence and mortality were estimated using delayed entry Cox proportional hazards models. Obese (30
 to &amp;lt;35&amp;nbsp;kg/m...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5537465</comments>
            <pubDate>Tue, 20 Dec 2011 16:48:15 +0100</pubDate>
            <guid isPermaLink="false">5537465</guid>        </item>
        <item>
            <title>Postoperative dose-dense sequential versus concomitant administration of epirubicin and paclitaxel in patients with node-positive breast cancer: 5-year results of the Hellenic Cooperative Oncology Group HE 10/00 phase III Trial</title>
            <link>http://www.medworm.com/index.php?rid=5537466&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F37667w63031554qg%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To explore the impact of dose intensity (DI) in the adjuvant setting of breast cancer, a randomized phase III trial was conducted
 comparing postoperative dose-dense sequential chemotherapy with epirubicin, paclitaxel, and cyclophosphamide, methotrexate
 and fluorouracil (CMF)in high-risk breast cancer patients. From Oct 2000 to June 2005, 1,121 node-positive patients were randomized
 to dose-dense sequential epirubicin 110&amp;nbsp;mg/m2 and paclitaxel (Taxol®, Bristol Myers-Squibb, Princeton, NJ) 250&amp;nbsp;mg/m2 (group A), or concurrent epirubicin 83&amp;nbsp;mg/m2 and paclitaxel 187&amp;nbsp;mg/m2 (group B), both followed by three cycles of “intensified” combination chemotherapy with CMF. By protocol design total cumulative
 dose and duration of treatment were identical in b...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5537466</comments>
            <pubDate>Tue, 20 Dec 2011 16:48:13 +0100</pubDate>
            <guid isPermaLink="false">5537466</guid>        </item>
        <item>
            <title>Early diagnostic protein biomarkers for breast cancer: how far have we come?</title>
            <link>http://www.medworm.com/index.php?rid=5515055&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe96388t8476350mp%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Many studies have used surface-enhanced laser desorption/ionization time-of-flight mass spectrometry or matrix-assisted laser
 desorption/ionization time-of-flight mass spectrometry to search for blood-based proteins that are related to the presence
 of breast cancer. We review the biomarkers discovered or targeted measured by these methods and discuss the strengths and
 weaknesses of these studies. We highlight two proteins that were most often related to breast cancer: C3a des-arginine anaphylatoxin
 (C3adesArg) (molecular weight: 8,938&amp;nbsp;Da) and fragments of inter-alpha trypsin inhibitor heavy chain H4 (ITIH4). In addition, we elaborate
 on three important methodological aspects related to these studies: protein identification, specificity of the markers, and
 dis...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5515055</comments>
            <pubDate>Fri, 16 Dec 2011 16:53:51 +0100</pubDate>
            <guid isPermaLink="false">5515055</guid>        </item>
        <item>
            <title>Risk of breast cancer in families of multiple affected women and men</title>
            <link>http://www.medworm.com/index.php?rid=5515056&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F615551371615hj65%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Family history of first and second-degree relatives is known to increase the risk for breast cancer. Less data are available
 on the risks between defined multiple affected close and distant relatives for which the reliability of data may be an issue.
 Data on affected males are sparse. These questions and the probable genetic models were addressed in this study by means of
 a nationwide Swedish Family-Cancer Database. We estimated the effect of family history of breast cancer by Poisson regression
 for women of at least 30&amp;nbsp;years of age after adjusting for age, period, region, socioeconomic status, number of children, and
 age at first birth. The results of the study showed that relative risk (RR) for breast cancer was associated with a first
 degree as well as sec...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5515056</comments>
            <pubDate>Fri, 16 Dec 2011 16:53:50 +0100</pubDate>
            <guid isPermaLink="false">5515056</guid>        </item>
        <item>
            <title>T cells sensitized with breast tumor progenitor cell vaccine have therapeutic activity against spontaneous HER2/neu tumors</title>
            <link>http://www.medworm.com/index.php?rid=5515057&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp00425t164366188%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cancer progenitor cells are critical for tumor initiation and recurrence so they are an important therapeutic target. We tested
 whether T cells could recognize tumor antigens expressed by breast cancer progenitor cells and acquire therapeutic activity
 against established metastases or delay onset of spontaneous tumors. Breast tumors were derived from HER2/neu transgenic mice and propagated in vitro under conditions that selected progenitor cells which were then used as an irradiated
 whole cell vaccine. A minor subset of recently sensitized T cells was isolated from vaccine-draining lymph nodes then activated
 in vitro to achieve numerical expansion. We show that the tumor progenitor cell vaccines reversed tolerance to a known HER2/neu epitope, otherwise inhibited by ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5515057</comments>
            <pubDate>Thu, 15 Dec 2011 16:49:07 +0100</pubDate>
            <guid isPermaLink="false">5515057</guid>        </item>
        <item>
            <title>A monoclonal antibody to the human HER3 receptor inhibits Neuregulin 1-beta binding and co-operates with Herceptin in inhibiting the growth of breast cancer derived cell lines</title>
            <link>http://www.medworm.com/index.php?rid=5515058&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl5520842h2wu467t%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The HER3 protein contributes to malignant transformation in breast and other cancer types as a consequence of elevated levels
 of expression, particularly in the presence of the HER2 protein. We show here that an antibody, called SGP1, to the extracellular
 domain of the HER3 receptor can inhibit completely Neuregulin stimulated growth of cultured breast cancer cells. Herceptin
 is a humanised monoclonal antibody to the HER2 protein which has an established role in the treatment of some patients with
 breast cancer. We demonstrate that Herceptin and SGP1 can bind simultaneously to breast cancer cells expressing both the HER2
 and HER3 proteins. In the presence of moderate levels of Herceptin, addition of the SGP1 monoclonal antibody gave a dose-dependent
 inhibition of ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5515058</comments>
            <pubDate>Wed, 14 Dec 2011 16:42:10 +0100</pubDate>
            <guid isPermaLink="false">5515058</guid>        </item>
        <item>
            <title>Integration of BRCA1-mediated miRNA and mRNA profiles reveals microRNA regulation of TRAF2 and NFκB pathway</title>
            <link>http://www.medworm.com/index.php?rid=5515059&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff225r81l61362173%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Microarray-based techniques are being useful to obtain miRNA and gene expression signatures associated with different tumors.
 BRCA1 deregulation is a frequent event in the pathogenesis of breast as well as other cancers. In addition to DNA repair functions
 of BRCA1, it is involved in a wide range of cellular processes such as cell cycle, chromatin remodeling or transcription.
 However, the molecular events underlying BRCA1-associated tumorigenesis are still largely unknown. In order to deepen our
 understanding of BRCA1-associated tumorigenesis, we integrated data from mRNA and miRNA microarray experiments on HCC1937 breast cancer cell line,
 and the isogenic HCC1937 stably expressing BRCA1, to obtain significant miRNA–mRNA relationships associated with the presence...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5515059</comments>
            <pubDate>Tue, 13 Dec 2011 17:03:38 +0100</pubDate>
            <guid isPermaLink="false">5515059</guid>        </item>
        <item>
            <title>A genetic risk predictor for breast cancer using a combination of low-penetrance polymorphisms in a Japanese population</title>
            <link>http://www.medworm.com/index.php?rid=5494612&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb371835u0v102707%2F</link>
            <description>In conclusion, we identified a genetic risk predictor of
 breast cancer in a Japanese population. Risk models which include a genetic risk score are possibly useful in distinguishing
 women at high risk of breast cancer from those at low risk, particularly in the context of targeted prevention.
 
 
	Content Type Journal ArticleCategory EpidemiologyPages 1-11DOI 10.1007/s10549-011-1904-5Authors
		Aiko Sueta, Division of Epidemiology and Prevention, Aichi Cancer Center Research Institute, 1-1, Kanokoden, Chikusa-ku, Nagoya, 464-8681 JapanHidemi Ito, Division of Epidemiology and Prevention, Aichi Cancer Center Research Institute, 1-1, Kanokoden, Chikusa-ku, Nagoya, 464-8681 JapanTakakazu Kawase, Division of Epidemiology and Prevention, Aichi Cancer Center Research Institute, 1-1, Kanokoden, C...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5494612</comments>
            <pubDate>Sat, 10 Dec 2011 16:55:14 +0100</pubDate>
            <guid isPermaLink="false">5494612</guid>        </item>
        <item>
            <title>Comparison of two nomograms to predict pathologic complete responses to neoadjuvant chemotherapy for breast cancer: evidence that HER2-positive tumors need specific predictors</title>
            <link>http://www.medworm.com/index.php?rid=5494613&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj7362h1316074370%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of this study is to compare two published nomograms, the “Institut Gustave Roussy/M.D. Anderson Cancer Center” (IGR/MDACC)
 and the Colleoni nomograms, in predicting pathologic complete responses (pCR) to preoperative chemotherapy in an independent
 cohort and to assess the impact of HER2 status. Data from 200 patients with breast carcinoma treated with preoperative chemotherapy
 were collected. We calculated pCR rate predictions with the two nomograms and compared the predictions with the outcomes.
 Sixty percent of the patients with HER2-positive tumors received trastuzumab concomitantly with taxanes. Model performances
 were quantified with respect to discrimination and calibration. In the whole population, the area under the ROC curve (AUC)
 for the IGR/...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5494613</comments>
            <pubDate>Thu, 08 Dec 2011 18:21:49 +0100</pubDate>
            <guid isPermaLink="false">5494613</guid>        </item>
        <item>
            <title>Ethanol promotes mammary tumor growth and angiogenesis: the involvement of chemoattractant factor MCP-1</title>
            <link>http://www.medworm.com/index.php?rid=5494616&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr66k771657266432%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Alcohol consumption is a risk factor for breast cancer in humans. Experimental studies indicate that alcohol exposure promotes
 malignant progression of mammary tumors. However, the underlying cellular and molecular mechanisms remain unclear. Alcohol
 induces a pro-inflammatory response by modulating the expression of cytokines and chemokines. Monocyte chemoattractant protein-1
 (MCP-1), also known as chemokine (C–C motif) ligand 2, is a pro-inflammatory chemokine implicated in breast cancer development/malignancy.
 We investigated the role of MCP-1 in alcohol-promoted mammary tumor progression. Using a xenograft model, we demonstrated
 that alcohol increased tumor angiogenesis and promoted growth/metastasis of breast cancer cells in C57BL/6 mice. Alcohol up-regulated...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5494616</comments>
            <pubDate>Thu, 08 Dec 2011 18:21:48 +0100</pubDate>
            <guid isPermaLink="false">5494616</guid>        </item>
        <item>
            <title>TIMP-1 in combination with HER2 and TOP2A for prediction of benefit from adjuvant anthracyclines in high-risk breast cancer patients</title>
            <link>http://www.medworm.com/index.php?rid=5494615&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2n477k45894r22n7%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 HER2 amplification, TOP2A aberrations, and absence of tissue inhibitor of metalloproteinase (TIMP-1) expression in breast carcinomas have been shown
 to be associated with incremental benefit from anthracycline-containing adjuvant chemotherapy, and this study was undertaken
 to validate these findings in a similar, but independent, randomized clinical trial. TIMP-1 was examined by immunohistochemistry
 in archival tumor tissue from 403 of 716 premenopausal high-risk patients with known HER2 and TOP2A status who were randomized to cyclophosphamide, epirubicin, and fluorouracil (CEF) or cyclophosphamide, methotrexate, and
 fluorouracil (CMF) in the MA.5 trial. Ninety-eight (24%) patients had no TIMP-1 staining of tumor cells, 27% were HER2 amplified, and 18% were TOP2A ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5494615</comments>
            <pubDate>Thu, 08 Dec 2011 18:21:48 +0100</pubDate>
            <guid isPermaLink="false">5494615</guid>        </item>
        <item>
            <title>Incremental increase in VEGFR1+ hematopoietic progenitor cells and VEGFR2+ endothelial progenitor cells predicts relapse and lack of tumor response in breast cancer patients</title>
            <link>http://www.medworm.com/index.php?rid=5494614&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa5513hr178425x17%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Animal models have demonstrated the critical role of bone marrow-derived VEGFR1+ hematopoietic progenitor cells (HPCs) and VEGFR2+ endothelial progenitor cells (EPCs) in metastatic progression. We explored whether these cells could predict relapse and
 response in breast cancer (BC) patients. One hundred and thirty-two patients with stages 1–4 BC were enrolled on 2 studies.
 Circulating CD45+/CD34+/VEGFR1+ HPCs and CD45dim/CD133+/VEGFR2+ EPCs were assessed from peripheral blood mononuclear cells using flow cytometry. Changes in HPCs and EPCs were analyzed in
 (1) patients without overt disease that relapsed and (2) metastatic patients according to response by RECIST. At study entry,
 102 patients were without evidence of disease and 30 patients had metastatic BC. Seve...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5494614</comments>
            <pubDate>Thu, 08 Dec 2011 18:21:48 +0100</pubDate>
            <guid isPermaLink="false">5494614</guid>        </item>
        <item>
            <title>Fingolimod potentiates the effects of sunitinib malate in a rat breast cancer model</title>
            <link>http://www.medworm.com/index.php?rid=5494618&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq37tg08m731l835k%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Most of the antiangiogenic strategies used in oncology principally target endothelial cells through the vascular endothelial
 growth factor (VEGF) pathway. Multiple kinase inhibitors can secondarily reduce mural cell stabilization of the vessels by
 blocking platelet-derived growth factor receptor (PDGFR) activity. However, sphingosine-1-phosphate (S1P), which is also implicated
 in mural cell recruitment, has yet to be targeted in clinical practice. We therefore investigated the potential of a simultaneous
 blockade of the PDGF and S1P pathways on the chemotactic responses of vascular smooth muscle cells (VSMCs) and the resulting
 effects of this blockade on breast tumor growth. Due to crosstalk between the S1P and PDGF pathways, we used AG1296 and/or
 VPC-23019 to inh...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5494618</comments>
            <pubDate>Thu, 08 Dec 2011 18:21:47 +0100</pubDate>
            <guid isPermaLink="false">5494618</guid>        </item>
        <item>
            <title>Multilevel determinants of breast cancer survival: association with geographic remoteness and area-level socioeconomic disadvantage</title>
            <link>http://www.medworm.com/index.php?rid=5494617&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq808057200112108%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A major priority for cancer control agencies is to reduce geographical inequalities in cancer outcomes. While the poorer breast
 cancer survival among socioeconomically disadvantaged women is well established, few studies have looked at the independent
 contribution that area- and individual-level factors make to breast cancer survival. Here, we examine relationships between
 geographic remoteness, area-level socioeconomic disadvantage and breast cancer survival after adjustment for patients’ socio-demographic
 characteristics and stage at diagnosis. Multilevel logistic regression and Markov chain Monte Carlo simulation were used to
 analyze 18,568 breast cancer cases extracted from the Queensland Cancer Registry for women aged 30–70&amp;nbsp;years diagnosed between
 19...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5494617</comments>
            <pubDate>Thu, 08 Dec 2011 18:21:47 +0100</pubDate>
            <guid isPermaLink="false">5494617</guid>        </item>
        <item>
            <title>Locoregional recurrence after breast cancer surgery: a systematic review by receptor phenotype</title>
            <link>http://www.medworm.com/index.php?rid=5486447&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdg4q568wk2183q68%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Molecular subtyping confirms that breast cancer comprises at least four genetically distinct entities based on the expression
 of specific genes including estrogen receptor (ER), progesterone receptor (PR), and HER2/neu receptor. The quantitative influence of subtype on ipsilateral locoregional recurrence (LRR) is unknown. The aim of this
 study was to systematically appraise the influence of breast cancer subtype on LRR following breast conserving therapy (BCT)
 and mastectomy. A comprehensive search for studies examining outcomes after BCT and/or mastectomy according to breast cancer
 subtype was performed using Medline and cross-referencing available data. Reviews of each study were conducted and data extracted
 to perform meta-analysis. Primary outcome was LRR relat...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5486447</comments>
            <pubDate>Tue, 06 Dec 2011 16:59:09 +0100</pubDate>
            <guid isPermaLink="false">5486447</guid>        </item>
        <item>
            <title>Evaluating breast cancer risk projections for Hispanic women</title>
            <link>http://www.medworm.com/index.php?rid=5486446&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm8580132741nl333%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;For Hispanic women, the Breast Cancer Risk Assessment Tool (BCRAT; “Gail Model”) combines 1990–1996 breast cancer incidence
 for Hispanic women with relative risks for breast cancer risk factors from non-Hispanic white (NHW) women. BCRAT risk projections
 have never been comprehensively evaluated for Hispanic women. We compared the relative risks and calibration of BCRAT risk
 projections for 6,353 Hispanic to 128,976 NHW postmenopausal participants aged 50 and older in the Women’s Health Initiative
 (WHI). Calibration was assessed by the ratio of the number of breast cancers observed with that expected by the BCRAT (O/E).
 We re-evaluated calibration for an updated BCRAT that combined BCRAT relative risks with 1993–2007 breast cancer incidence
 that is contem...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5486446</comments>
            <pubDate>Tue, 06 Dec 2011 16:59:09 +0100</pubDate>
            <guid isPermaLink="false">5486446</guid>        </item>
        <item>
            <title>GPER mediates the Egr-1 expression induced by 17β-estradiol and 4-hydroxitamoxifen in breast and endometrial cancer cells</title>
            <link>http://www.medworm.com/index.php?rid=5486445&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Feg10l2682346x32j%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Early growth response-1 (Egr-1) is an immediate early gene involved in relevant biological events including the proliferation
 of diverse types of cell tumors. In a microarray analysis performed in breast cancer cells, 17β-estradiol (E2) and the estrogen
 receptor antagonist 4-hydroxitamoxifen (OHT) up-regulated Egr-1 through the G protein-coupled receptor named GPR30/GPER. Hence,
 in this study, we aimed to provide evidence regarding the ability of E2, OHT and the selective GPER ligand G-1 to regulate
 Egr-1 expression and function through the GPER/EGFR/ERK transduction pathway in both Ishikawa (endometrial) and SkBr3 (breast)
 cancer cells. Interestingly, we demonstrate that Egr-1 is involved in the transcription of genes regulating cell proliferation
 like CTGF and ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5486445</comments>
            <pubDate>Tue, 06 Dec 2011 16:59:09 +0100</pubDate>
            <guid isPermaLink="false">5486445</guid>        </item>
        <item>
            <title>Melatonin pathway genes and breast cancer risk among Chinese women</title>
            <link>http://www.medworm.com/index.php?rid=5476159&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3687q65rv7787088%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Previous studies suggest that melatonin may act on cancer growth through a variety of mechanisms, most notably by direct anti-proliferative
 effects on breast cancer cells and via interactions with the estrogen pathway. Three genes are largely responsible for mediating
 the downstream effects of melatonin: melatonin receptors 1a and 1b (MTNR1a and MTNR1b), and arylalkylamine N-acetyltransferase (AANAT). It is hypothesized that genetic variation in these genes may lead to altered protein production or function. To address
 this question, we conducted a comprehensive evaluation of the association between common single nucleotide polymorphisms (SNPs)
 in the MTNR1a, MTNR1b, and AANAT genes and breast cancer risk among 2,073 cases and 2,083 controls, using a two-stage analy...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5476159</comments>
            <pubDate>Fri, 02 Dec 2011 18:09:34 +0100</pubDate>
            <guid isPermaLink="false">5476159</guid>        </item>
        <item>
            <title>Phase 2 study of neoadjuvant treatment with NOV-002 in combination with doxorubicin and cyclophosphamide followed by docetaxel in patients with HER-2 negative clinical stage II–IIIc breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5476160&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj86063323v66h30n%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;NOV-002 (a formulation of disodium glutathione disulfide) modulates signaling pathways involved in tumor cell proliferation
 and metastasis and enhances anti-tumor immune responsiveness in tumor models. The addition of NOV-002 to chemotherapy has
 been shown to increase anti-tumor efficacy in animal models and some early phase oncology trials. We evaluated the clinical
 effects of NOV-002 in primary breast cancer, whether adding NOV-002 to standard preoperative chemotherapy increased pathologic
 complete response rates (pCR) at surgery, and determined whether NOV-002 mitigated hematologic toxicities of chemotherapy
 and whether levels of myeloid derived suppressor cells (MDSC) were predictive of response. Forty-one women with newly diagnosed
 stages II–IIIc HER-2 nega...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5476160</comments>
            <pubDate>Fri, 02 Dec 2011 18:09:32 +0100</pubDate>
            <guid isPermaLink="false">5476160</guid>        </item>
        <item>
            <title>Progression of ductal carcinoma in situ to invasive breast cancer is associated with gene expression programs of EMT and myoepithelia</title>
            <link>http://www.medworm.com/index.php?rid=5476162&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff8l50452382np711%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ductal carcinoma in situ (DCIS) is a precursor lesion that can gives rise to invasive breast cancer (IBC). It has been proposed
 that both the nature of the lesion and the tumor microenvironment play key roles in progression to IBC. Here, laser capture
 microdissected tissue from pure DCIS and pure IBC were employed to define key gene expression profiles in either the epithelial
 or stromal compartment associated with disease progression. Each tissue had distinct gene expression profiles, and a DCIS/IBC
 classifier accurately distinguished DCIS versus IBC in multiple independent data sets. However, contrary to other studies
 that profiled DCIS associated with invasive disease, we found that the most significant alterations in gene expression were
 observed in the epithe...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5476162</comments>
            <pubDate>Thu, 01 Dec 2011 19:29:06 +0100</pubDate>
            <guid isPermaLink="false">5476162</guid>        </item>
        <item>
            <title>Lack of association between common single nucleotide polymorphisms in the TERT-CLPTM1L locus and breast cancer in women of African ancestry</title>
            <link>http://www.medworm.com/index.php?rid=5476161&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp5568806227952t1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;As one of the most common cancers worldwide, breast cancer places an extraordinary burden on the populations of African ancestry.
 Common SNPs in the TERT-CLPTM1L locus have been reported to be associated with several types of cancer, including breast cancer. We sought to investigate
 whether the previously reported common single nucleotide polymorphisms (SNPs) in the TERT-CLPTM1L locus could also contribute to the breast cancer risk in women of African ancestry. We genotyped eleven SNPs in 2,892 women
 of African descent but were unable to detect any significant association between TERT-CLPTM1L SNPs and their predispositions for breast cancer risk. Given the differences in linkage disequilibrium patterns across populations,
 our findings suggest that larger independent...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5476161</comments>
            <pubDate>Thu, 01 Dec 2011 19:29:06 +0100</pubDate>
            <guid isPermaLink="false">5476161</guid>        </item>
        <item>
            <title>Vitamin D intake, vitamin D receptor polymorphisms, and breast cancer risk among women living in the southwestern U.S.</title>
            <link>http://www.medworm.com/index.php?rid=5476163&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe77l507q560w3601%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;No studies of dietary vitamin D intake and vitamin D receptor (VDR) have been conducted comparing breast risk among Hispanic
 women and non-Hispanic white (NHW) women. We investigated the association between vitamin D intake and breast cancer in a
 population-based case–control study of 1,527 NHW and 791 Hispanic breast cancer cases diagnosed in 1999–2004 in Arizona, New
 Mexico, Utah, and Colorado, and 1,599 NHW and 922 Hispanic age-matched controls. Vitamin D intake was assessed using food
 frequency questionnaires, and associations with breast cancer were adjusted for age, ethnicity, state, education, body mass
 index, smoking, age at menarche, age at first birth, parity, hormone exposure, height, and physical activity using logistic
 regression. BsmI, Poly A and...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5476163</comments>
            <pubDate>Wed, 30 Nov 2011 18:41:13 +0100</pubDate>
            <guid isPermaLink="false">5476163</guid>        </item>
        <item>
            <title>Associated expressions of FGFR-2 and FGFR-3: from mouse mammary gland physiology to human breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5456987&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F20gn6486t2710265%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Fibroblast growth factor receptors (FGFRs) are tyrosine kinase receptors which have been implicated in breast cancer. The
 aim of this study was to evaluate FGFR-1, -2, -3, and -4 protein expressions in normal murine mammary gland development, and
 in murine and human breast carcinomas. Using immunohistochemistry and Western blot, we report a hormonal regulation of FGFR
 during postnatal mammary gland development. Progestin treatment of adult virgin mammary glands resulted in changes in localization
 of FGFR-3 from the cytoplasm to the nucleus, while treatment with 17-β-estradiol induced changes in the expressions and/or
 localizations of FGFR-2 and -3. In murine mammary carcinomas showing different degrees of hormone dependence, we found progestin-induced
 increased e...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5456987</comments>
            <pubDate>Mon, 28 Nov 2011 16:51:10 +0100</pubDate>
            <guid isPermaLink="false">5456987</guid>        </item>
        <item>
            <title>A CD44−/CD24+ phenotype is a poor prognostic marker in early invasive breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5456988&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbr5h0g6622106943%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A CD44−/CD24+ phenotype is a poor prognostic marker in early invasive breast cancer. Breast cancer cells with high CD44 and low or absent
 CD24 (i.e. CD44+CD24−/low phenotype) are reported to have stem cell features. However, the clinical impact of CD24 and CD44 expression in tumours
 remains unclear. To explore the immunohistochemical expression of CD44 and CD24 (individually and combined) and their clinical
 value as prognostic and predictive markers. Immunohistochemical expression of CD24 and CD44 was studied in a large series
 of early primary invasive breast cancer tumours (n&amp;nbsp;=&amp;nbsp;1036) prepared as a tissue microarray. Associations between the expression of each marker individually and in combination
 and clinico-pathological, molecular variables and pat...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5456988</comments>
            <pubDate>Sat, 26 Nov 2011 16:48:56 +0100</pubDate>
            <guid isPermaLink="false">5456988</guid>        </item>
        <item>
            <title>Surgical treatment of early stage breast cancer in elderly: an international comparison</title>
            <link>http://www.medworm.com/index.php?rid=5456989&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F3666555k06k004m7%2F</link>
            <description>This study showed large international differences
 in treatment of elderly early stage breast cancer patients, with the most striking result the large proportion of elderly
 who did not undergo surgery at all. Despite large treatment differences, survival does not seem to be affected in a major
 way.
 
 
	Content Type Journal ArticleCategory EpidemiologyPages 1-8DOI 10.1007/s10549-011-1892-5Authors
		M. Kiderlen, Department of Surgery, Leiden University Medical Center, P.O. Box 9600, 2300 RC, Leiden, The NetherlandsE. Bastiaannet, Department of Surgery, Leiden University Medical Center, P.O. Box 9600, 2300 RC, Leiden, The NetherlandsP. M. Walsh, National Cancer Registry, Cork, IrelandN. L. Keating, Brigham and Women’s Hospital and Harvard Medical School, Boston, USAS. Schrodi, Munich Can...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5456989</comments>
            <pubDate>Sat, 26 Nov 2011 16:48:55 +0100</pubDate>
            <guid isPermaLink="false">5456989</guid>        </item>
        <item>
            <title>Somatic mutations in the BRCA1 gene in Chinese women with sporadic breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5449540&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F46608077655757k3%2F</link>
            <description>In this study, we detected BRCA1 somatic mutations in tumor cDNA from 144 Chinese women with sporadic breast cancer by using polymerase chain reaction (PCR)-direct
 sequencing assay. In total, eight BRCA1 alterations (three nonsense mutations and five missense mutations) were identified in this cohort of 144 sporadic breast
 cancers. We further confirmed that 5 out of 144(3.5%) sporadic breast cancer cases carried a BRCA1 somatic mutation, including two novel nonsense mutations (c.191_212del22 and c.2963C&amp;gt;G) resulting in a truncated protein
 and three missense mutations (c.114G&amp;gt;T, c.925A&amp;gt;C, and c.824G&amp;gt;A). The two cases with BRCA1 somatic truncating mutations also contained a TP53 somatic mutation in the tumors. Our study suggested that a small subset of sporadic breast cancers ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449540</comments>
            <pubDate>Thu, 24 Nov 2011 17:52:32 +0100</pubDate>
            <guid isPermaLink="false">5449540</guid>        </item>
        <item>
            <title>Phenocopy breast cancer rates in Israeli BRCA1BRCA2 mutation carrier families: is the risk increased in non-carriers?</title>
            <link>http://www.medworm.com/index.php?rid=5449542&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5k57p2157963638u%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;
 BRCA1 and BRCA2 mutation carriers have an increased risk for developing breast (and ovarian) cancer. Non-carriers from within such families
 (=true negatives) are counseled that their risk for developing breast cancer is similar to that of the average-risk population.
 Breast cancer diagnosed in a non-carrier from a family with a known mutation is coined phenocopy. The rate of breast cancer
 phenocopy and the risk for breast cancer in true negatives are unsettled. The rate of phenocopy breast cancer was assessed
 in non-carriers from Jewish families with a BRCA1 or BRCA2 mutation, identified at the Sheba medical center. Analysis was performed by t test for comparison of mean age at counseling or breast cancer diagnosis, and by calculating a standardized incidence rati...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449542</comments>
            <pubDate>Wed, 23 Nov 2011 17:36:19 +0100</pubDate>
            <guid isPermaLink="false">5449542</guid>        </item>
        <item>
            <title>BRCA1 c.4987-3C&gt;G is a pathogenic mutation</title>
            <link>http://www.medworm.com/index.php?rid=5449541&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd661h94566128715%2F</link>
            <description>BRCA1 c.4987-3C&gt;G is a pathogenic mutation
	Content Type Journal ArticleCategory Letter to the EditorPages 1-3DOI 10.1007/s10549-011-1878-3Authors
		Rita D. Brandão, Department of Clinical Genetics, University Hospital of Maastricht, P.O. Box 616, 6200 MD Maastricht, The NetherlandsKees E. P. van Roozendaal, Department of Clinical Genetics, University Hospital of Maastricht, P.O. Box 616, 6200 MD Maastricht, The NetherlandsDemis Tserpelis, Department of Clinical Genetics, University Hospital of Maastricht, P.O. Box 616, 6200 MD Maastricht, The NetherlandsBeppy Caanen, Department of Clinical Genetics, University Hospital of Maastricht, P.O. Box 616, 6200 MD Maastricht, The NetherlandsEncarna Gómez García, Department of Clinical Genetics, University Hospital of Maastricht, P.O. Box 616, 6...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449541</comments>
            <pubDate>Wed, 23 Nov 2011 17:36:19 +0100</pubDate>
            <guid isPermaLink="false">5449541</guid>        </item>
        <item>
            <title>Impact of a telephone-based physical activity intervention upon exercise behaviors and fitness in cancer survivors enrolled in a cooperative group setting</title>
            <link>http://www.medworm.com/index.php?rid=5449543&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl178297716182216%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Observational studies demonstrate an association between physical activity and improved outcomes in breast and colon cancer
 survivors. To test these observations with a large, randomized clinical trial, an intervention that significantly impacts
 physical activity in these patients is needed. The Active After Cancer Trial (AACT) was a multicenter pilot study evaluating
 the feasibility of a telephone-based exercise intervention in a cooperative group setting. Sedentary (engaging in &amp;lt;60&amp;nbsp;min
 of recreational activity/week) breast and colorectal cancer survivors were randomized to a telephone-based exercise intervention
 or usual care control group. The intervention was delivered through the University of California at San Diego; participants
 received ten phone c...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449543</comments>
            <pubDate>Wed, 23 Nov 2011 17:36:17 +0100</pubDate>
            <guid isPermaLink="false">5449543</guid>        </item>
        <item>
            <title>Twenty-five year results of the national cancer institute randomized breast conservation trial</title>
            <link>http://www.medworm.com/index.php?rid=5449544&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4345h61285602537%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Breast conservation therapy (BCT) consisting of lumpectomy and postoperative radiation has become an accepted alternative
 to mastectomy (MRM) for the treatment of early stage breast cancer. We currently report the 25&amp;nbsp;year outcomes of a single institution,
 prospective, randomized clinical trial at the National Cancer Institute. 237 women with pathologically confirmed invasive
 breast tumors 5&amp;nbsp;cm or less were accrued between 1979 and 1987 and randomized to receive either BCT or MRM. Overall survival
 was the primary endpoint. Patients with node positive disease were included and treated with doxorubicin and cyclophosphamide.
 Both arms received axillary dissection. BCT patients had radiation to the whole breast followed by a boost. At a median follow-up
 of 25...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449544</comments>
            <pubDate>Wed, 23 Nov 2011 17:36:16 +0100</pubDate>
            <guid isPermaLink="false">5449544</guid>        </item>
        <item>
            <title>Beyond taxanes: the next generation of microtubule-targeting agents</title>
            <link>http://www.medworm.com/index.php?rid=5449545&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fkt74009663220417%2F</link>
            <description>This article reviews these alternative microtubule-targeting agents and their potential
 clinical benefits for MBC patients. Relevant clinical data were compiled through searches within PubMed and congress abstract
 databases. Ixabepilone, a novel microtubule-stabilizing drug approved by the US Food and Drug Administration (FDA), has proven
 efficacy across multiple lines of therapy, including patients with taxane-resistant/refractory disease. In phase III trials,
 ixabepilone plus capecitabine significantly improved progression-free survival compared with capecitabine alone in anthracycline/taxane-pretreated
 patients. Eribulin has recently been approved by the FDA and by the European Medicines Agency for the treatment of patients
 with MBC who have received at least two prior chemotherap...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449545</comments>
            <pubDate>Wed, 23 Nov 2011 17:36:15 +0100</pubDate>
            <guid isPermaLink="false">5449545</guid>        </item>
        <item>
            <title>Investigation of human JC and BK polyomaviruses in breast carcinomas</title>
            <link>http://www.medworm.com/index.php?rid=5449546&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fqk70305262t266r2%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We have previously showed the presence of the simian virus 40 (SV40) and the mouse mammary tumor virus (MMTV)-like in a significant
 proportions of Tunisian breast carcinomas. However, to date there are no published studies concerning evaluation of the possible
 implication of the human polyomaviruses JC (JCV) and BK (BKV) in breast carcinomas. The presence of JCV and BKV DNA was investigated
 by PCR in a 123 primary breast carcinomas and matched adjacent non-tumor breast tissues. The results were correlated to clinicopathological
 and virological parameters. JCV T-antigen DNA was detected in 23% of breast carcinoma cases; however, all cases were negative
 for BKV. JCV T antigen PCR products were further confirmed as authentic JCV genome by direct sequencing. JCV was fo...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449546</comments>
            <pubDate>Tue, 22 Nov 2011 17:58:26 +0100</pubDate>
            <guid isPermaLink="false">5449546</guid>        </item>
        <item>
            <title>An in vitro investigation of metabolically sensitive biomarkers in breast cancer progression</title>
            <link>http://www.medworm.com/index.php?rid=5440343&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fnx3w7801x2748360%2F</link>
            <description>In this study, we used microarray data from the GEO database to compare gene expression for regulators
 of metabolism and epigenetic alterations among non-invasive epithelial (MCF-7, MDA-MB-361, and T-47D) and invasive mesenchymal
 (MDA-MB-231, Hs-578T, and BT-549) breast cancer cell lines. The expression of genes, including GLS1, GFPT2, LDHA, HDAC9, MYST2, and SUV420H2, was assessed using RT-PCR. There was differential expression between epithelial and mesenchymal cell lines. MYST2 and SUV420H2 regulate the levels of the epigenetic biomarkers histone H4 lysine 16 acetylation (H4K16ac) and histone H4 lysine 20 trimethylation
 (H4K20me3), respectively. Reduced amounts of H4K16ac and H4K20me3 correlated with lower levels of MYST2 and SUV420H2 in mesenchymal cells and, along with reduced amou...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5440343</comments>
            <pubDate>Sat, 19 Nov 2011 06:52:21 +0100</pubDate>
            <guid isPermaLink="false">5440343</guid>        </item>
        <item>
            <title>Prediction of menopausal status from estrogen-related gene expression in benign breast tissue</title>
            <link>http://www.medworm.com/index.php?rid=5431358&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr40g33725822u2j8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The utility of archived paraffin-embedded breast tissue for risk-related research is often limited by missing menopausal status
 data. We tested the hypothesis that breast tissue gene expression patterns can improve menopausal stratification. Healthy
 high-risk participants in a clinical trial underwent breast random fine-needle aspiration (rFNA); 100&amp;nbsp;ng of RNA extracted
 from rFNA samples was reverse-transcribed; the expression of 28 estrogen-responsive genes was evaluated by real-time PCR.
 True menopausal status (TMS) was determined by measurement of plasma hormones and age. Differentially expressed genes and
 age were analyzed by logistic regression. The accuracy of the menopause prediction was assessed using receiver-operator characteristic
 (ROC) analysis, an...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5431358</comments>
            <pubDate>Fri, 18 Nov 2011 17:33:01 +0100</pubDate>
            <guid isPermaLink="false">5431358</guid>        </item>
        <item>
            <title>Phase II trial of preoperative paclitaxel, gemcitabine, and trastuzumab combination therapy in HER2 positive stage II/III breast cancer: The Korean Cancer Study Group BR 07-01</title>
            <link>http://www.medworm.com/index.php?rid=5431360&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff40780473n967017%2F</link>
            <description>This study was designed to evaluate the efficacy and safety of preoperative paclitaxel,
 gemcitabine, and trastuzumab (PGH) combination for HER2-positive breast caner. Pathologically, proven node positive stage
 II/III breast cancer patients with adequate organ function and no history of anti-cancer therapy were eligible. Patients received
 weekly trastuzumab with paclitaxel 80&amp;nbsp;mg/m2 and gemcitabine 1,200&amp;nbsp;mg/m2 on days 1 and 8, every 3&amp;nbsp;weeks for 6 cycles. Postoperatively, patients completed trastuzumab for 1&amp;nbsp;year and hormone therapy
 for 5&amp;nbsp;years if indicated. All patients received postoperative radiation therapy. Of 53 enrolled patients with a median tumor
 of 5.3 (range, 2.0 to &amp;gt;12) cm; 43.4%, T3/T4; 75.4%, N2/N3; and 45.3%, positive hormone receptors. The path...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5431360</comments>
            <pubDate>Fri, 18 Nov 2011 06:54:11 +0100</pubDate>
            <guid isPermaLink="false">5431360</guid>        </item>
        <item>
            <title>A comparative biomarker study of 514 matched cases of male and female breast cancer reveals gender-specific biological differences</title>
            <link>http://www.medworm.com/index.php?rid=5431359&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy5717082400p4231%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Male breast cancer remains understudied despite evidence of rising incidence. Using a co-ordinated multi-centre approach,
 we present the first large scale biomarker study to define and compare hormone receptor profiles and survival between male
 and female invasive breast cancer. We defined and compared hormone receptor profiles and survival between 251 male and 263
 female breast cancers matched for grade, age, and lymph node status. Tissue microarrays were immunostained for ERα, ERβ1,
 -2, -5, PR, PRA, PRB and AR, augmented by HER2, CK5/6, 14, 18 and 19 to assist typing. Hierarchical clustering determined
 differential nature of influences between genders. Luminal A was the most common phenotype in both sexes. Luminal B and HER2
 were not seen in males. Basal pheno...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5431359</comments>
            <pubDate>Fri, 18 Nov 2011 06:54:11 +0100</pubDate>
            <guid isPermaLink="false">5431359</guid>        </item>
        <item>
            <title>Individually tailored treatment with epirubicin and paclitaxel with or without capecitabine as first-line chemotherapy in metastatic breast cancer: a randomized multicenter trial</title>
            <link>http://www.medworm.com/index.php?rid=5431361&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx636j02lh1ln8w34%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Anthracyclines and taxanes are active cytotoxic drugs in the treatment of early metastatic breast cancer. It is yet unclear
 whether addition of capecitabine to the combination of these drugs improves the treatment outcome. Patients with advanced
 breast cancer were randomized to first-line chemotherapy with a combination of epirubicin (Farmorubicin®) and paclitaxel (Taxol®) alone (ET) or in combination with capecitabine (Xeloda®, TEX). Starting doses for ET were epirubicin 75&amp;nbsp;mg/m2 plus paclitaxel 175&amp;nbsp;mg/m2, and for TEX epirubicin 75&amp;nbsp;mg/m2, paclitaxel 155&amp;nbsp;mg/m2, and capecitabine 825&amp;nbsp;mg/m2 BID for 14&amp;nbsp;days. Subsequently, doses were tailored related to side effects. Primary endpoint was progression-free survival
 (PFS); secondary endpoints...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5431361</comments>
            <pubDate>Fri, 18 Nov 2011 06:54:09 +0100</pubDate>
            <guid isPermaLink="false">5431361</guid>        </item>
        <item>
            <title>Serum enterolactone levels and mortality outcome in women with early breast cancer: a retrospective cohort study</title>
            <link>http://www.medworm.com/index.php?rid=5431362&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw866262vl1375825%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We previously demonstrated that high serum enterolactone levels are associated with a reduced incidence of breast cancer in
 healthy women. The present study was aimed at investigating whether a similar association might be found between serum enterolactone
 levels and the mortality of women with early breast cancer. The levels of enterolactone in cryopreserved serum aliquots obtained
 from 300 patients, operated on for breast cancer, were measured using a time-resolved fluoro-immunoassay. Levels were analyzed
 in respect to the risk of mortality following surgery. Cox proportional hazard regression models were used to check for prognostic
 features, to estimate hazard ratios for group comparisons and to test for the interaction on mortality hazards between the
 variabl...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5431362</comments>
            <pubDate>Fri, 18 Nov 2011 06:54:08 +0100</pubDate>
            <guid isPermaLink="false">5431362</guid>        </item>
        <item>
            <title>High miR-26a and low CDC2 levels associate with decreased EZH2 expression and with favorable outcome on tamoxifen in metastatic breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5431363&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd70q54l18533n100%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;For patients with metastatic breast cancer, we previously described that increased EZH2 expression levels were associated
 with an adverse outcome to tamoxifen therapy. Main objective of the present study is to investigate miR-26a and miR-101 levels,
 which both target EZH2, for their association with molecular pathways and with efficacy of tamoxifen as first-line monotherapy
 for metastatic breast cancer. Expression levels were measured using quantitative Real-Time Polymerase Chain Reaction (qRT-PCR)
 in primary breast cancer specimens of 235 estrogen receptor-α (ER)-positive patients. Pathway analysis was performed on microarray
 data available for 65 of these tumors. Logistic regression and Cox uni- and multivariate analysis were performed to relate
 expression leve...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5431363</comments>
            <pubDate>Fri, 18 Nov 2011 06:54:07 +0100</pubDate>
            <guid isPermaLink="false">5431363</guid>        </item>
        <item>
            <title>Effect of simvastatin on the pharmacokinetics of anastrozole</title>
            <link>http://www.medworm.com/index.php?rid=5421616&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh2710221140h7411%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We have prospectively tested the effects of simvastatin on the pharmacokinetics of anastrozole and on estrogen concentrations
 in postmenopausal women with hormone receptor-positive breast cancer who were receiving adjuvant anastrozole. Following 14
 days of simvastatin, we did not observe a significant change in plasma concentrations of anastrozole or hydroxyanastrozole
 in nine evaluable women. Likewise, we did not observe any statistically significant change in serum concentrations of either
 estradiol, which remained in the undetectable range, or estrone sulfate. Simvastatin and anastrozole may be safely co-administered.
 Pharmacokinetic results suggest that simvastatin is not likely to compromise the activity of anastrozole.
 
 
	Content Type Journal ArticleCategor...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5421616</comments>
            <pubDate>Wed, 16 Nov 2011 16:48:14 +0100</pubDate>
            <guid isPermaLink="false">5421616</guid>        </item>
        <item>
            <title>Breast epithelial cell proliferation is markedly increased with short-term high levels of endogenous estrogen secondary to controlled ovarian hyperstimulation</title>
            <link>http://www.medworm.com/index.php?rid=5421617&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F96870251luu52072%2F</link>
            <description>We report in this article our studies comparing cell proliferation, Ki67 (MIB1), and estrogen and progesterone receptor levels
 (ERα, PRA, and PRB) in the breast terminal duct lobular units of oocyte donors, women in early pregnancy, and in normally
 cycling women. Breast tissue and blood samples were obtained from 10 oocyte donors, and 30 pregnant women at 5–18&amp;nbsp;weeks of
 gestation. Breast tissue samples were also obtained from 26 normally cycling women. In the oocyte donors: peak E2 (mean&amp;nbsp;~15,300&amp;nbsp;pmol/l)
 was reached on the day before oocyte (and tissue) donation; peak progesterone (P4; mean 36.3&amp;nbsp;nmol/l) was reached on the day
 of donation; Ki67 was positively associated with level of E2, and the mean Ki67 was 7.0% significantly greater than the mean
 1.8% of cyclin...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5421617</comments>
            <pubDate>Mon, 14 Nov 2011 16:55:47 +0100</pubDate>
            <guid isPermaLink="false">5421617</guid>        </item>
        <item>
            <title>A phase II study of 17-allylamino-17-demethoxygeldanamycin in metastatic or locally advanced, unresectable breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5421618&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq2v5128341q45800%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Heat shock protein 90 (Hsp90) is an attractive target for breast cancer treatment, as it is required for the proper folding
 and stabilization of several proteins known to be involved in breast cancer growth and development. These proteins include
 the epidermal growth factor receptor, human epidermal growth factor receptor 2 (HER2), estrogen receptor (ER), progesterone
 receptor (PR), and src. 17-Allylamino-17-demethoxygeldanamycin (17-AAG) is an intravenous Hsp90 inhibitor in development for
 breast cancer treatment. We conducted a phase II study of 17-AAG 220&amp;nbsp;mg/m2 on days 1, 4, 8, and 11 every 21&amp;nbsp;days in patients with metastatic and locally advanced breast cancer. Since we expected the
 molecular effects of Hsp90 inhibition to extend beyond just ER, PR, an...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5421618</comments>
            <pubDate>Mon, 14 Nov 2011 16:55:46 +0100</pubDate>
            <guid isPermaLink="false">5421618</guid>        </item>
        <item>
            <title>Case report and review of the literature: Secretory breast cancer in a 13-year-old boy—10 years of follow up</title>
            <link>http://www.medworm.com/index.php?rid=5421619&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8355286717kq2230%2F</link>
            <description>We report a case of male secretory breast
 carcinoma in a 13-year-old boy. Radical mastectomy was performed followed by chemotherapy. The patient is free of disease
 after 10&amp;nbsp;years. Secretory breast carcinoma (SBC) is the commonest type of breast carcinoma in children. In this article, we
 discuss the diagnosis and treatment options for breast cancer among children as well as features of SBC, based on a literature
 review.
 
 
	Content Type Journal ArticleCategory ReviewPages 1-8DOI 10.1007/s10549-011-1869-4Authors
		Cesar Cabello, University of Campinas (UNICAMP), Av. Alexander Flemming, 101, Cidade Universitária, Campinas, SP 13083-881, BrazilMarcelo Alvarenga, Pathology Institute of Campinas (IPC), Campinas, BrazilCesar Augusto Alvarenga, Pathology Institute of Campinas (IPC), Cam...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5421619</comments>
            <pubDate>Mon, 14 Nov 2011 16:55:45 +0100</pubDate>
            <guid isPermaLink="false">5421619</guid>        </item>
        <item>
            <title>Topoisomerase 2A gene amplification in breast cancer. Critical evaluation of different FISH probes</title>
            <link>http://www.medworm.com/index.php?rid=5421620&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff331q18n16436871%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The HER2 amplicon on chromosome 17q is variable in size and occasionally includes Topoisomerase 2A (TOP2A) at 17q21-22. It has been suggested that TOP2 co-amplification, not HER2 amplification on chromosome 17q11.2-12, is a useful predictive marker of response to anthracycline-based chemotherapy in
 breast cancer patients. Given the significant toxicities of anthracyclines, the detection methods of TOP2A gene amplifications have to be standardized. We determined TOP2A gene alterations using two different fluorescence in situ hybridization (FISH) DNA probes. HER2 amplifications were identified
 with the PathVysion™ probe. TOP2A status of 42 HER2 amplified breast cancers was tested by FISH with PathVysion™ covering 160&amp;nbsp;kb and DAKO pharm DX™ covering
 228&amp;nbsp;k...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5421620</comments>
            <pubDate>Mon, 14 Nov 2011 16:55:43 +0100</pubDate>
            <guid isPermaLink="false">5421620</guid>        </item>
        <item>
            <title>Endocrine therapy in obese patients with primary breast cancer: another piece of evidence in an unfinished puzzle</title>
            <link>http://www.medworm.com/index.php?rid=5407158&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe66m3565l07l8377%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Obesity, defined as a body mass index (BMI) ≥30 is an independent risk factor in breast cancer and is correlated with shorter
 survival and enhanced recurrence rates. The present subgroup analysis of the German BRENDA-cohort aimed to investigate the
 correlation between BMI, recurrence-free survival (RFS) and adjuvant endocrine therapy. In this subgroup analysis, 4,636 patients
 were retrospectively examined using multivariate analyses. Overall 3,759 (81.1%) patients had a BMI &amp;lt;30 (non-obese) and 877
 (18.9%) a BMI ≥30 (obese). In the group of all 3,896 (84.0%) patients with hormone-receptor-positive (HR+) breast carcinomas
 a significant reduction in RFS was demonstrated for those who were obese (P&amp;nbsp;=&amp;nbsp;0.002; HR&amp;nbsp;=&amp;nbsp;1.45 (95% CI: 1.15–1.83)), a...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407158</comments>
            <pubDate>Sat, 12 Nov 2011 16:53:12 +0100</pubDate>
            <guid isPermaLink="false">5407158</guid>        </item>
        <item>
            <title>Cadherin–catenin complex dissociation in lobular neoplasia of the breast</title>
            <link>http://www.medworm.com/index.php?rid=5407157&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F723m0k332762h214%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;E-cadherin (E-CD) inactivation with loss of E-CD-mediated cell adhesion is the hallmark of lesions of the lobular phenotype.
 E-CD is typically absent by immunohistochemistry in both lobular carcinoma in situ (LCIS) and invasive lobular lesions, suggesting
 it occurs early in the neoplastic process. In laboratory models, downstream post-transcriptional modifiers such as TWIST and
 SNAIL contribute to the dissociation of the intracellular component of the cadherin–catenin complex (CCC), resulting in tumor
 progression and invasion. We hypothesized that complete CCC dissociation may play a role in lobular neoplasia progression.
 Here we explore the relationship between loss of E-CD and dissociation of the CCC in pure LCIS and LCIS associated with invasive
 cancer. Fresh...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407157</comments>
            <pubDate>Sat, 12 Nov 2011 16:53:12 +0100</pubDate>
            <guid isPermaLink="false">5407157</guid>        </item>
        <item>
            <title>Pathologic features and molecular phenotype by patient age in a large cohort of young women with breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5407159&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw4ru481066614l24%2F</link>
            <description>We examined the pathologic features and distribution of molecular phenotype in relation to patient age in a large group of
 young women (≤40&amp;nbsp;years) with invasive breast cancer. Medical records were reviewed for clinical characteristics, tumor stage,
 and receptor status. Pathologic features, including those features associated with basal-like carcinomas, were examined by
 central review. Using tumor grade and biomarker expression, cancers were categorized as luminal A (ER+ and/or PR+ and HER2−,
 histologic grade 1 or 2); luminal B (ER+ and/or PR+ and HER2+, or ER and/or PR+, HER2− and grade 3); HER2 (ER and PR− and
 HER2+); and triple negative (ER−, PR−, and HER2−). Among 399 women&amp;nbsp;of ≤40&amp;nbsp;years, 33% had luminal A tumors, 35% luminal B,
 11% HER2 (ER-negative)...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407159</comments>
            <pubDate>Sat, 12 Nov 2011 16:53:11 +0100</pubDate>
            <guid isPermaLink="false">5407159</guid>        </item>
        <item>
            <title>Paclitaxel sensitivity of breast cancer cells requires efficient mitotic arrest and disruption of Bcl-xL/Bak interaction</title>
            <link>http://www.medworm.com/index.php?rid=5407160&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv1580275418n5l6l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Taxanes are being used for the treatment of breast cancer. However, cancer cells frequently develop resistance to these drugs
 with the subsequent recurrence of the tumor. MDA-MB-231 and T-47D breast cancer cell lines were used to assess the effect
 of paclitaxel treatment on apoptosis and cell cycle, the possible mechanisms of paclitaxel resistance as well as the enhancement
 of paclitaxel-induced apoptosis based on its combination with phenylethyl isothiocyanate (PEITC). T-47D cells undergo apoptosis
 in response to paclitaxel treatment. The induction of apoptosis was associated with a robust mitotic arrest and the disruption
 of Bcl-xL/Bak interaction. By contrary, MDA-MB-231 cells were insensitive to paclitaxel-induced apoptosis and this was associated
 with a high ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407160</comments>
            <pubDate>Thu, 10 Nov 2011 16:49:53 +0100</pubDate>
            <guid isPermaLink="false">5407160</guid>        </item>
        <item>
            <title>Correlation of white female breast cancer incidence trends with nitrogen dioxide emission levels and motor vehicle density patterns</title>
            <link>http://www.medworm.com/index.php?rid=5407161&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F407t95506720r6n1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The long-term trend of female breast cancer incidence rates in the United States and some European countries demonstrates
 a similar pattern: an increasing trend in the last century followed by a declining trend in this century. The well-known risk
 factors cannot explain this trend. We compared the breast cancer incidence trends obtained from SEER data with the trend of
 nitrogen dioxides (NOx) emission and monitoring data as well as motor vehicle density data. The upward followed by downward
 trend of NOx is similar to the breast cancer incidence trend but with an offset of 20&amp;nbsp;years earlier. Motor vehicles are the
 major source of NOx emissions. The geographic distribution of motor vehicles density in 1970 in the observed US counties is
 positively correlated wit...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407161</comments>
            <pubDate>Thu, 10 Nov 2011 16:49:52 +0100</pubDate>
            <guid isPermaLink="false">5407161</guid>        </item>
        <item>
            <title>Risk prediction models of breast cancer: a systematic review of model performances</title>
            <link>http://www.medworm.com/index.php?rid=5407162&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb622l86r7258j756%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The number of risk prediction models has been increasingly developed, for estimating about breast cancer in individual women.
 However, those model performances are questionable. We therefore have conducted a study with the aim to systematically review
 previous risk prediction models. The results from this review help to identify the most reliable model and indicate the strengths
 and weaknesses of each model for guiding future model development. We searched MEDLINE (PubMed) from 1949 and EMBASE (Ovid)
 from 1974 until October 2010. Observational studies which constructed models using regression methods were selected. Information
 about model development and performance were extracted. Twenty-five out of 453 studies were eligible. Of these, 18 developed
 prediction mod...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407162</comments>
            <pubDate>Thu, 10 Nov 2011 16:49:51 +0100</pubDate>
            <guid isPermaLink="false">5407162</guid>        </item>
        <item>
            <title>Expression of SPRR3 is associated with tumor cell proliferation in less advanced stages of breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5407163&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F310035w847578085%2F</link>
            <description>This study demonstrates that SPRR3 promotes
 BC cell proliferation by enhancing p53 degradation via the AKT and MAPK pathways and is, therefore, a potential novel therapeutic
 target for less advanced stages of BC.
 
 
	Content Type Journal ArticleCategory Preclinical StudyPages 1-8DOI 10.1007/s10549-011-1868-5Authors
		Jin Cheon Kim, Department of Surgery, University of Ulsan College of Medicine, Seoul, Republic of KoreaJong Han Yu, Department of Surgery, University of Ulsan College of Medicine, Seoul, Republic of KoreaYoon Kyung Cho, Department of Surgery, University of Ulsan College of Medicine, Seoul, Republic of KoreaChoon Sik Jung, Department of Surgery, University of Ulsan College of Medicine, Seoul, Republic of KoreaSei Hyun Ahn, Department of Surgery, University of Ulsan College o...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407163</comments>
            <pubDate>Thu, 10 Nov 2011 16:49:50 +0100</pubDate>
            <guid isPermaLink="false">5407163</guid>        </item>
        <item>
            <title>The CIRAS study: a case control study to define the clinical, immunologic, and radiographic features of aromatase inhibitor-induced musculoskeletal symptoms</title>
            <link>http://www.medworm.com/index.php?rid=5407164&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fjtv843q53l618561%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Aromatase inhibitors (AIs) are widely prescribed for post-menopausal hormone receptor-positive breast cancer; however, musculoskeletal
 symptoms limit their tolerability. The purpose of this study was to determine whether joint pain in women receiving AIs is
 associated with inflammatory arthritis as measured by the disease activity score-28 (DAS-28), and to evaluate association
 with tenosynovitis on ultrasound. A total of 48 postmenopausal women with stage I–III breast cancer and hand pain were recruited
 from the Lombardi Comprehensive Cancer Center. Those receiving AIs were cases (n&amp;nbsp;=&amp;nbsp;25), and those not receiving AIs were controls (n&amp;nbsp;=&amp;nbsp;23). During a single study visit, subjects underwent blinded rheumatologic evaluation, DAS-28, health assessme...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407164</comments>
            <pubDate>Thu, 10 Nov 2011 16:49:48 +0100</pubDate>
            <guid isPermaLink="false">5407164</guid>        </item>
        <item>
            <title>A short-term biomarker modulation study of simvastatin in women at increased risk of a new breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5407165&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr69807770841378x%2F</link>
            <description>This study demonstrates the feasibility of short-term biomarker
 modulation studies using the contralateral breast of high-risk women. Simvastatin appears to modulate estrone sulfate concentrations
 and its potential chemopreventive activity in breast cancer warrants further investigation.
 
 
	Content Type Journal ArticleCategory Clinical TrialPages 1-10DOI 10.1007/s10549-011-1858-7Authors
		Michaela J. Higgins, The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, 1650 Orleans Street, CRBI, Room 144, Baltimore, MD 21231, USATatiana M. Prowell, The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, 1650 Orleans Street, CRBI, Room 144, Baltimore, MD 21231, USAAmanda L. Blackford, The Sidney Kimmel Comprehensive Canc...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407165</comments>
            <pubDate>Thu, 10 Nov 2011 16:49:47 +0100</pubDate>
            <guid isPermaLink="false">5407165</guid>        </item>
        <item>
            <title>The association between mammographic density measures and aspirin or other NSAID use</title>
            <link>http://www.medworm.com/index.php?rid=5407166&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8032214052425408%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;There is evidence that aspirin use reduces the risk of breast cancer. Increased mammographic density is known to be associated
 with increased breast cancer risk. Little is known about the association between mammographic density and aspirin or other
 non-steroidal anti-inflammatory drug (NSAID) use, but it is possible that the association between aspirin use and breast cancer
 risk might be due to the effect of aspirin on mammographic density. Multiple linear regression was used to investigate the
 association between measures of mammographic density and the use, frequency, and duration of aspirin and other NSAIDs such
 as paracetamol (acetaminophen), arthritis medication, and other over-the-counter or doctor-prescribed pain medications in
 3286 women from the Australi...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407166</comments>
            <pubDate>Tue, 08 Nov 2011 19:12:33 +0100</pubDate>
            <guid isPermaLink="false">5407166</guid>        </item>
        <item>
            <title>Prognostic role of CA15.3 in 7942 patients with operable breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5407167&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff686p0kq5431p368%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;To assess the prognostic value of presurgical CA15.3 in a large cohort of patients with early breast cancer. A total of 7.942
 consecutive patients with breast cancer operated at the European Institute of Oncology between 1998 and 2005 and with presurgical
 values of CA 15.3 available were included. We explored patterns of recurrence by baseline CA 15.3 values. Mean CA15.3 was
 17.0&amp;nbsp;U/ml. CA15.3 was associated with age, tumor size, nodal involvement, Ki-67 labeling index, grade, HER2 expression, molecular
 subtype, and perivascular invasion. CA15.3 was independently associated with distant metastases [HR&amp;nbsp;&amp;gt;&amp;nbsp;20&amp;nbsp;U/ml vs. ≤&amp;nbsp;20&amp;nbsp;U/ml:
 1.34 (95% CI 1.15–1.56)] and death [HR&amp;nbsp;&amp;gt;&amp;nbsp;20&amp;nbsp;U/ml vs. ≤&amp;nbsp;20&amp;nbsp;U/ml: 1.30 (95% C...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407167</comments>
            <pubDate>Tue, 08 Nov 2011 06:50:43 +0100</pubDate>
            <guid isPermaLink="false">5407167</guid>        </item>
        <item>
            <title>Adjuvant therapy for HER2+ breast cancer: practice, perception, and toxicity</title>
            <link>http://www.medworm.com/index.php?rid=5407168&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0440744625784160%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Multiple adjuvant regimens are used for HER2+ breast cancer, but experience in routine practice is not reported. We evaluated
 whether oncologists’ perceptions of these regimens matches clinical experience. We surveyed Wisconsin medical oncologists
 throughout the state regarding factors impacting selection of TCH (docetaxel, carboplatin, and trastuzumab) or anthracycline-based
 therapy. We also reviewed 200 cases of HER2+ breast cancer treated at the University of Wisconsin and the Marshfield Clinic
 and collected data on patient and tumor characteristics, chemotherapy regimen, and toxicities. Two-thirds of surveyed oncologists
 prefer anthracycline-based therapy, particularly for node-positive cancers. However, TCH was preferred for early-stage (T1a-bN0)
 tumors. Ha...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5407168</comments>
            <pubDate>Mon, 07 Nov 2011 17:12:16 +0100</pubDate>
            <guid isPermaLink="false">5407168</guid>        </item>
        <item>
            <title>Local treatment of mixed osteolytic/osteoblastic spinal metastases: is photodynamic therapy effective?</title>
            <link>http://www.medworm.com/index.php?rid=5384590&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fmtw541v2745q8050%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The widespread use of systemic and local therapies aimed at spinal metastatic lesions secondary to breast cancer has increased
 the incidence of mixed osteolytic/osteoblastic patterns of bony disease. The complex structure of these lesions requires novel
 therapeutic approaches to both reduce tumor burden and restore structural stability. In photodynamic therapy (PDT), a minimally
 invasive approach can be used to employ light to activate a photosensitizing agent that preferentially accumulates in tumor
 tissue, leading to cell toxicity and death. Previous work in an osteolytic rat model (MT-1) demonstrated that PDT effectively
 ablates tumor and improves vertebral structural properties. The aim of this study was to assess the efficacy of PDT in a rat
 model of mixed os...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384590</comments>
            <pubDate>Sat, 05 Nov 2011 17:09:15 +0100</pubDate>
            <guid isPermaLink="false">5384590</guid>        </item>
        <item>
            <title>High level of miR-21, miR-10b, and miR-31 expression in bilateral vs. unilateral breast carcinomas</title>
            <link>http://www.medworm.com/index.php?rid=5384591&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx0g0905k4l6367v8%2F</link>
            <description>This study suggests that bilateral breast tumors have somewhat distinct pattern of molecular events as compared
 to the unilateral disease.
 
 
	Content Type Journal ArticleCategory Brief ReportPages 1-11DOI 10.1007/s10549-011-1845-zAuthors
		Aglaya G. Iyevleva, Laboratory of Molecular Oncology, N. N. Petrov Institute of Oncology, Pesochny-2, 197758 St.-Petersburg, RussiaEkatherina Sh. Kuligina, Laboratory of Molecular Oncology, N. N. Petrov Institute of Oncology, Pesochny-2, 197758 St.-Petersburg, RussiaNathalia V. Mitiushkina, Laboratory of Molecular Oncology, N. N. Petrov Institute of Oncology, Pesochny-2, 197758 St.-Petersburg, RussiaAlexandr V. Togo, Laboratory of Molecular Oncology, N. N. Petrov Institute of Oncology, Pesochny-2, 197758 St.-Petersburg, RussiaYoshio Miki, Department o...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384591</comments>
            <pubDate>Fri, 04 Nov 2011 16:54:39 +0100</pubDate>
            <guid isPermaLink="false">5384591</guid>        </item>
        <item>
            <title>Role of interleukin-10 in breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5384593&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm67h6g3qm440802r%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cytokines are low molecular weight regulatory proteins or glycoprotein that modulates the intensity and duration of immune
 response by stimulating or inhibiting the activation, proliferation, and/or differentiation of target cells. Different cytokines
 are known to have diverse role in breast cancer initiation and progression. Interleukin-10 (IL-10), a pleiotropic anti-inflammatory
 cytokine, induces immunosuppression and assists in escape from tumor immune surveillance. Like several other cytokines, IL-10
 also can exert dual proliferative and inhibitory effect on breast tumor cells indicating a complex role of IL-10 in breast
 cancer initiation and progression. In this review, we tried to put together a comprehensive current view on significance of
 IL-10 in promotio...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384593</comments>
            <pubDate>Fri, 04 Nov 2011 16:54:38 +0100</pubDate>
            <guid isPermaLink="false">5384593</guid>        </item>
        <item>
            <title>Ultrasonographic differentiation of malignant from benign breast lesions: a meta-analytic comparison of elasticity and BIRADS scoring</title>
            <link>http://www.medworm.com/index.php?rid=5384592&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F677v13103071p292%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;There has been controversy regarding the accuracy of breast ultrasound elastography (USE) compared to conventional B-mode
 Ultrasound (USB). The purpose of this study was to conduct a direct comparative effectiveness analysis of USB versus USE or
 their combination in differentiating breast lesions through systematically reviewing recent literature. An extensive literature
 search of PubMed and other medical and general purpose databases from inception through August 2011 was conducted. Published
 studies that reported a direct comparison of the diagnostic performance of USE, using elasticity score versus USB, using breast
 imaging reporting and data system (BIRADS) for characterization of focal breast lesions were included. Summary diagnostic
 performance measures were...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384592</comments>
            <pubDate>Fri, 04 Nov 2011 16:54:38 +0100</pubDate>
            <guid isPermaLink="false">5384592</guid>        </item>
        <item>
            <title>Detection of a large rearrangement in PALB2 in Spanish breast cancer families with male breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5384594&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg634203102222552%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;It has been demonstrated that monoallelic PALB2 (Partner and Localizer of BRCA2) gene mutations predispose to familial breast cancer. Some of the families reported with
 germline PALB2 mutations presented male breast cancer as a characteristic clinical feature. Therefore, we wanted to investigate the contribution
 of germline PALB2 mutations in a set of 131 Spanish BRCA1/BRCA2-negative breast/ovarian cancer families with at least one male breast cancer case. The analysis included direct sequencing
 of all coding exons and intron/exon boundaries as well as a Multiplex Ligation-dependent Probe Amplification-based analysis
 of genomic rearrangements. For the first time we have identified a genomic rearrangement of PALB2 gene involving a large deletion from exon 7 to 11 in ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384594</comments>
            <pubDate>Thu, 03 Nov 2011 16:55:59 +0100</pubDate>
            <guid isPermaLink="false">5384594</guid>        </item>
        <item>
            <title>Identification of copy number alterations associated with the progression of DCIS to invasive ductal carcinoma</title>
            <link>http://www.medworm.com/index.php?rid=5384595&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F02811k6466v08324%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Ductal carcinoma in situ (DCIS) is a non-obligate precursor to invasive ductal carcinoma (IDC). Annotation of the genetic
 differences between the two lesions may assist in the identification of genes that promote the invasive phenotype. Synchronous
 DCIS and IDC cells were microdissected from FFPE tissue and analysed by molecular inversion probe (MIP) copy number arrays.
 Matched IDC and DCIS showed highly similar copy number profiles (average of 83% of the genome shared) indicating a common
 clonal origin although there is evidence that the DCIS continues to evolve in parallel with the co-existing IDC. Four chromosomal
 regions of loss (3q, 6q, 8p and 11q) and four regions of gain (5q, 16p, 19q and 20) were recurrently affected in IDC but not
 in DCIS. CCND1 and MYC s...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384595</comments>
            <pubDate>Thu, 03 Nov 2011 16:55:58 +0100</pubDate>
            <guid isPermaLink="false">5384595</guid>        </item>
        <item>
            <title>Hormone therapy use and mammographic density in postmenopausal Norwegian women</title>
            <link>http://www.medworm.com/index.php?rid=5384596&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fpv74vv36m0v2l256%2F</link>
            <description>We examined whether mammographic density differed by type of hormone
 therapy (HT) used, dose, duration of use, time since last use, and whether the effects are modified by age and body mass index
 (BMI). Using a cross-sectional design, we recruited 2,424 postmenopausal women aged 50–69&amp;nbsp;years participating in the Norwegian
 Breast Cancer Screening Program. Mammographic density was assessed with a computer-assisted method, and we estimated mean
 absolute and percent mammographic density through multiple linear regression, and adjusting for possible confounders. Mammographic
 density was higher among current HT users (percent density: 22.6%; 95% CI: 22.1–23.2%) than among former (17.7%; 17.2–18.2%)
 or never users (16.3%; 15.7–16.8%). The highest density was seen in current EPT ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384596</comments>
            <pubDate>Thu, 03 Nov 2011 16:55:57 +0100</pubDate>
            <guid isPermaLink="false">5384596</guid>        </item>
        <item>
            <title>Erratum to: The BRCA2 c.9004G&gt;A (E3002K) variant is likely pathogenic and recurs in breast and/or ovarian cancer families of French Canadian descent</title>
            <link>http://www.medworm.com/index.php?rid=5384598&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft40518821327h666%2F</link>
            <description>Erratum to: The BRCA2 c.9004G&gt;A (E3002K) variant is likely pathogenic and recurs in breast and/or ovarian cancer families of French Canadian descent
	Content Type Journal ArticleCategory ErratumPages 1-1DOI 10.1007/s10549-011-1830-6Authors
		Stephanie Cote, Service de Médecine Génique, Département de Médecine, Centre Hospitalier de l’Université de Montréal, Montreal, CanadaSuzanna L. Arcand, The Research Institute of the McGill University Health Centre, Montreal, CanadaRobert Royer, Department of Public Health, Women’s College Research Institute, The University of Toronto, Toronto, CanadaSerge Nolet, Département de Pathologie, Centre Hospitalier de l’Université de Montréal, Montreal, CanadaAnne-Marie Mes-Masson, Institut du cancer de Montréal, Centre de Recherche du Centre ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384598</comments>
            <pubDate>Wed, 02 Nov 2011 16:57:46 +0100</pubDate>
            <guid isPermaLink="false">5384598</guid>        </item>
        <item>
            <title>Differential oxidative status and immune characterization of the early and advanced stages of human breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5384597&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F351461j430064085%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Breast cancer is the malignant neoplasia with the highest incidence in women worldwide. Chronic oxidative stress and inflammation
 have been indicated as major mediators during carcinogenesis and cancer progression. Human studies have not considered the
 complexity of tumor biology during the stages of cancer advance, limiting their clinical application. The purpose of this
 study was to characterize systemic oxidative stress and immune response parameters in early (ED; TNM I and II) and advanced
 disease (AD; TNM III and IV) of patients diagnosed with infiltrative ductal carcinoma breast cancer. Oxidative stress parameters
 were evaluated by plasmatic lipoperoxidation, carbonyl content, thiobarbituric reactive substances (TBARS), nitric oxide levels
 (NO), total radica...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384597</comments>
            <pubDate>Wed, 02 Nov 2011 16:57:46 +0100</pubDate>
            <guid isPermaLink="false">5384597</guid>        </item>
        <item>
            <title>Basal-like Breast cancer DNA copy number losses identify genes involved in genomic instability, response to therapy, and patient survival</title>
            <link>http://www.medworm.com/index.php?rid=5384599&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj4p86628831x2px3%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Breast cancer is a heterogeneous disease with known expression-defined tumor subtypes. DNA copy number studies have suggested
 that tumors within gene expression subtypes share similar DNA Copy number aberrations (CNA) and that CNA can be used to further
 sub-divide expression classes. To gain further insights into the etiologies of the intrinsic subtypes, we classified tumors
 according to gene expression subtype and next identified subtype-associated CNA using a novel method called SWITCHdna, using
 a training set of 180 tumors and a validation set of 359 tumors. Fisher’s exact tests, Chi-square approximations, and Wilcoxon
 rank-sum tests were performed to evaluate differences in CNA by subtype. To assess the functional significance of loss of
 a specific chromosom...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384599</comments>
            <pubDate>Wed, 02 Nov 2011 16:57:45 +0100</pubDate>
            <guid isPermaLink="false">5384599</guid>        </item>
        <item>
            <title>Ki-67: level of evidence and methodological considerations for its role in the clinical management of breast cancer: analytical and critical review</title>
            <link>http://www.medworm.com/index.php?rid=5384600&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr4k1405650171084%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Clinicians can use biomarkers to guide therapeutic decisions in estrogen receptor positive (ER+) breast cancer. One such biomarker
 is cellular proliferation as evaluated by Ki-67. This biomarker has been extensively studied and is easily assayed by histopathologists
 but it is not currently accepted as a standard. This review focuses on its prognostic and predictive value, and on methodological
 considerations for its measurement and the cut-points used for treatment decision. Data describing study design, patients’
 characteristics, methods used and results were extracted from papers published between January 1990 and July 2010. In addition,
 the studies were assessed using the REMARK tool. Ki-67 is an independent prognostic factor for disease-free survival (HR 1.05...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384600</comments>
            <pubDate>Wed, 02 Nov 2011 16:57:44 +0100</pubDate>
            <guid isPermaLink="false">5384600</guid>        </item>
        <item>
            <title>Women’s features and inter-/intra-rater agreement on mammographic density assessment in full-field digital mammograms (DDM-SPAIN)</title>
            <link>http://www.medworm.com/index.php?rid=5384601&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb20x664864642172%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Measurement of mammographic density (MD), one of the leading risk factors for breast cancer, still relies on subjective assessment.
 However, the consistency of MD measurement in full-digital mammograms has yet to be evaluated. We studied inter- and intra-rater
 agreement with respect to estimation of breast density in full-digital mammograms, and tested whether any of the women’s characteristics
 might have some influence on them. After an initial training period, three experienced radiologists estimated MD using Boyd
 scale in a left breast cranio-caudal mammogram of 1,431 women, recruited at three Spanish screening centres. A subgroup of
 50 randomly selected images was read twice to estimate short-term intra-rater agreement. In addition, a reading of 1,428 of
 the...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384601</comments>
            <pubDate>Mon, 31 Oct 2011 16:53:00 +0100</pubDate>
            <guid isPermaLink="false">5384601</guid>        </item>
        <item>
            <title>Triggering of Toll-like receptor 4 on metastatic breast cancer cells promotes αvβ3-mediated adhesion and invasive migration</title>
            <link>http://www.medworm.com/index.php?rid=5384603&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj0324r248v73215g%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Triggering of Toll-like receptor 4 (TLR4) on tumor cells has been found to promote tumor progression by promoting tumor cell
 proliferation and survival. So far, however, the effect of TLR4 signaling on tumor metastasis has not been well elucidated.
 Here, we report that triggering of TLR4 on metastatic breast cancer cells could reciprocally regulate the expression of αvβ3
 and the expressions of TPM1 and maspin, and promote αvβ3-mediated adhesion and invasive migration of the cells. In metastatic
 breast cancer cells, TLR4 signaling increased the expression of integrin αvβ3 by activating NF-κB, resulting in the increased
 adhesion capacity of tumor cells to the ligand for αvβ3, and the increased polymerization of actin and production of MMP-9
 in tumor cells i...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384603</comments>
            <pubDate>Mon, 31 Oct 2011 16:52:59 +0100</pubDate>
            <guid isPermaLink="false">5384603</guid>        </item>
        <item>
            <title>Comparison of breast cancer recurrence risk and cardiovascular disease incidence risk among postmenopausal women with breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5384602&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft5m3360750876q83%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The majority of breast cancers are diagnosed in postmenopausal women. Competing comorbidities, particularly cardiovascular
 disease (CVD), should be considered when individualizing adjuvant therapies for these women. We compared the 10-year predicted
 breast cancer recurrence risk with CVD risk among postmenopausal women with hormone receptor-positive (HR+), non-metastatic
 breast cancer. CVD risk factor data were prospectively collected from postmenopausal women with stage I-III, HR+&amp;nbsp;breast cancer
 initiating adjuvant aromatase inhibitor therapy. We compared predicted 10-year CVD risk, including the composite index heart
 age, computed from modified Framingham risk score, with predicted 10-year risk of breast cancer recurrence using Adjuvant!
 Online. We created m...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384602</comments>
            <pubDate>Mon, 31 Oct 2011 16:52:59 +0100</pubDate>
            <guid isPermaLink="false">5384602</guid>        </item>
        <item>
            <title>A phase I/II prospective, single arm trial of gefitinib, trastuzumab, and docetaxel in patients with stage IV HER-2 positive metastatic breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5384605&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh375xx8852w7071l%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Inhibition of the HER-2 pathway via the monoclonal antibody trastuzumab has had a major impact in treatment of HER-2 positive
 breast cancer, but de novo or acquired resistance may reduce its effectiveness. The known interplay between the epidermal
 growth factor receptor (EGFR) and HER-2 receptors and pathways creates a rationale for combined anti-EGFR and anti-HER-2 therapy
 in HER-2 positive metastatic breast cancer (MBC), and toxicities associated with the use of multiple chemotherapeutic agents
 together with biological therapies may also be reduced. We conducted a prospective, single arm, phase I/II trial to determine
 the efficacy and toxicity of the combination of trastuzumab with the EGFR inhibitor gefitinib and docetaxel, in patients with
 HER-2 positive MBC. ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384605</comments>
            <pubDate>Mon, 31 Oct 2011 16:52:57 +0100</pubDate>
            <guid isPermaLink="false">5384605</guid>        </item>
        <item>
            <title>Chromosome 17 centromere (CEP17) duplication as a predictor of anthracycline response: evidence from the NCIC Clinical Trials Group (NCIC CTG) MA.5 Trial</title>
            <link>http://www.medworm.com/index.php?rid=5384604&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fru50wxu8078qw432%2F</link>
            <description>This study suggests that
 CEP17 duplication has a borderline association with clinical responsiveness to anthracycline containing chemotherapy similar
 to previous results seen with HER2 amplification and TOP2A alteration in MA.5. An appropriately powered meta-analysis is required to discriminate the predictive value of these three
 candidate markers.
 
 
	Content Type Journal ArticleCategory Clinical trialPages 1-11DOI 10.1007/s10549-011-1840-4Authors
		Kathleen I. Pritchard, Sunnybrook Odette Cancer Centre, The University of Toronto, 2075 Bayview Avenue, Toronto, ON M4N 3M5, CanadaAlison Munro, Endocrine Cancer Group, Edinburgh Cancer Research Centre, Western General Hospital, Crewe Road South, Edinburgh, EH4 2XR UKFrances P. O’Malley, University of Toronto, Toronto, ON, CanadaDongshen...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384604</comments>
            <pubDate>Mon, 31 Oct 2011 16:52:57 +0100</pubDate>
            <guid isPermaLink="false">5384604</guid>        </item>
        <item>
            <title>Epstein–Barr virus is seldom found in mammary epithelium of breast cancer tissue using in situ molecular methods</title>
            <link>http://www.medworm.com/index.php?rid=5384606&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg63374w05584u723%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Epstein–Barr virus (EBV) has been proposed as a possible etiological agent of breast cancer based on 21 reports of EBV in
 malignant breast tissues. Most of these studies used standard and nested solution polymerase chain reaction (PCR) techniques,
 both disadvantaged by susceptibility to contamination from laboratory EBV, and the inability to localize the signal to a specific
 cell type. To avoid these issues, we used in situ molecular methods of viral detection to reassess the frequency of EBV in
 malignant breast tissue. We used a commercial in situ hybridization (ISH) system with an EBER genome target, and a non-commercial
 in situ PCR (IS-PCR) method using primers specific for the BamH1 region. The assays were performed on malignant breast tissue sections from 70...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384606</comments>
            <pubDate>Mon, 31 Oct 2011 16:52:55 +0100</pubDate>
            <guid isPermaLink="false">5384606</guid>        </item>
        <item>
            <title>Comparison between screen-detected and symptomatic breast cancers according to molecular subtypes</title>
            <link>http://www.medworm.com/index.php?rid=5384609&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff4025237127u5602%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Breast cancer screening programs make it possible to detect early cancer, thus reducing breast cancer mortality. We studied
 the clinicopathologic characteristics and prognosis of screen-detected invasive breast cancer compared with symptomatic breast
 cancer. And we compared the result according to molecular subtypes (luminal A, luminal B, Her2, and triple negative), with
 the goal of identifying the role of screening in each subtypes. From January 2002 to June 2008, 3,141 patients who underwent
 surgery for the treatment of invasive ductal carcinoma at Samsung Medical Center were included. Among them, 1,025 patients
 were screen-detected, and 2,116 patients who were screened over 2&amp;nbsp;years or never were symptomatic. We retrospectively reviewed
 the clinical and pat...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384609</comments>
            <pubDate>Mon, 31 Oct 2011 16:52:54 +0100</pubDate>
            <guid isPermaLink="false">5384609</guid>        </item>
        <item>
            <title>Rates of upgrade to malignancy for 271 cases of flat epithelial atypia (FEA) diagnosed by breast core biopsy</title>
            <link>http://www.medworm.com/index.php?rid=5384608&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy1j231733734j1t5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Flat epithelial atypia (FEA) is a borderline lesion that might represent an early stage in the development of certain low-grade
 carcinomas in situ and invasive cancers. There are no guidelines on its management. Our objectives were to determine the upgrade
 to malignancy rate and identify a subpopulation of patients that might undergo just mammographic surveillance. We retrospectively
 reviewed the data for 271 FEA cases among 5,555 breast core biopsies obtained over a 7-year period (January 2003–2010). We
 collated clinical data (age, history of cancer, menopausal status), radiological data (lesion type, size, Bi-Rads category),
 technical data (number of biopsies, needle gauge, excision quality) and histological data and sought correlations between
 these factors a...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384608</comments>
            <pubDate>Mon, 31 Oct 2011 16:52:54 +0100</pubDate>
            <guid isPermaLink="false">5384608</guid>        </item>
        <item>
            <title>A plea for the biopsy marker: how, why and why not clipping after breast biopsy?</title>
            <link>http://www.medworm.com/index.php?rid=5384607&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0435vh12n78r3636%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;In the last decade, percutaneous breast biopsies have become a standard for the management of breast diseases. Biopsy clips
 allow for precise lesion localization, thus minimizing the volume of breast to be resected at the time of surgery. With the
 development of many imaging techniques (including mammography, sonography, and breast magnetic resonance imaging), one of
 the challenges of the multidisciplinary became to synthesize all informations obtained from the various imaging procedures.
 The use of biopsy markers after percutaneous biopsy is one of the keys for optimal patient management, helping the radiologist
 to deal with multiple lesions, to insure correlation across different imaging modalities and to follow-up benign lesions,
 helping the oncologist by marki...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384607</comments>
            <pubDate>Mon, 31 Oct 2011 16:52:54 +0100</pubDate>
            <guid isPermaLink="false">5384607</guid>        </item>
        <item>
            <title>Breast tenderness and breast cancer risk in the estrogen plus progestin and estrogen-alone women’s health initiative clinical trials</title>
            <link>http://www.medworm.com/index.php?rid=5384611&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn6x3130l2t61u884%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The associations between breast tenderness during use of conjugated equine estrogen (CEE) therapy with or without medroxyprogesterone
 (MPA) therapy and subsequent breast cancer risk are unknown. We analyzed data from the Women’s Health Initiative Estrogen
 plus Progestin (N&amp;nbsp;=&amp;nbsp;16,608, 5.6&amp;nbsp;years intervention) and estrogen-alone (N&amp;nbsp;=&amp;nbsp;10,739, 6.8&amp;nbsp;years intervention) clinical trials until trial close-out (Spring 2005). At baseline and annually, participants
 underwent mammography and clinical breast exam. Self-reported breast tenderness was assessed at baseline and 12&amp;nbsp;months. Invasive
 breast cancer was confirmed by medical record review. The risk of new-onset breast tenderness after 12&amp;nbsp;months was significantly
 higher among women a...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384611</comments>
            <pubDate>Mon, 31 Oct 2011 16:52:53 +0100</pubDate>
            <guid isPermaLink="false">5384611</guid>        </item>
        <item>
            <title>Epigenetic silencing of the tumor suppressor klotho in human breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5384610&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn756174657145157%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Klotho is a single pass transmembrane protein, associated with premature aging. We identified tumor suppressor activities
 for klotho, associated with reduced expression in breast cancer. We now aimed to analyze klotho expression in early stages
 of breast tumorigenesis and elucidate mechanisms leading to klotho silencing in breast tumors. We studied klotho expression,
 using immunohistochemistry, and found high klotho expression in all normal and mild hyperplasia samples, whereas reduced expression
 was associated with moderate and atypical ductal hyperplasia. Promoter methylation and histone deacetylation were studied
 as possible mechanisms for klotho silencing. Using bisulfite sequencing, and methylation-specific PCR, we identified KLOTHO promoter methylation in fiv...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384610</comments>
            <pubDate>Mon, 31 Oct 2011 16:52:53 +0100</pubDate>
            <guid isPermaLink="false">5384610</guid>        </item>
        <item>
            <title>Polymorphisms in cycloxygenase-2 gene and breast cancer prognosis: association between PTGS2 haplotypes and histopathological features</title>
            <link>http://www.medworm.com/index.php?rid=5384612&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fwn236x1567818863%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Cyclooxygenase-2 (COX-2) overexpression is associated with worse prognosis in breast cancer. COX-2 is encoded by a polymorphic
 gene, called PTGS2, and its expression may be genetically influenced. In this article, we investigate the association between PTGS2 haplotypes and histopathological parameters with prognostic value on the clinical outcome of breast cancer. The study involved
 606 women under current treatment for non-metastatic breast cancer. Patients were genotyped for rs689465, rs689466, rs20417,
 and rs5275, and their haplotypes were inferred. The distribution of PTGS2 genotypes and haplotypes was evaluated according to histopathological categorical groups used for prognostic determination
 of low/intermediate versus high risk of tumor recurrence. Our result...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384612</comments>
            <pubDate>Sun, 30 Oct 2011 05:37:48 +0100</pubDate>
            <guid isPermaLink="false">5384612</guid>        </item>
        <item>
            <title>Regarding “Co-expression of SNAIL and TWIST determines prognosis in estrogen receptor-positive early breast cancer patients”</title>
            <link>http://www.medworm.com/index.php?rid=5384614&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg8j77713704p8567%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s10549-011-1831-5Authors
		Hiu-Fung Yuen, Center for Cancer Research and Cell Biology, Queen’s University of Belfast, Belfast, BT9 7BL UKShu-Dong Zhang, Center for Cancer Research and Cell Biology, Queen’s University of Belfast, Belfast, BT9 7BL UKAshley San-Yu Wong, Department of Pathology, The University of Hong Kong, Hong Kong, HKSAR, ChinaCian M. McCrudden, Center for Cancer Research and Cell Biology, Queen’s University of Belfast, Belfast, BT9 7BL UKYu-Han Huang, Institute of Molecular and Cell Biology, A*STAR, Singapore, SingaporeKelvin Yuen-Kwong Chan, Department of Pathology, The University of Hong Kong, Hong Kong, HKSAR, ChinaMohamed El-Tanani, Center for Cancer Research and Cell Biology, Queen...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384614</comments>
            <pubDate>Sat, 29 Oct 2011 05:47:00 +0100</pubDate>
            <guid isPermaLink="false">5384614</guid>        </item>
        <item>
            <title>Lipidomic approach to identify patterns in phospholipid profiles and define class differences in mammary epithelial and breast cancer cells</title>
            <link>http://www.medworm.com/index.php?rid=5384613&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fgj70x1w8hn010481%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Breast cancer is the leading cause of cancer-related deaths in women. Altered cellular functions of cancer cells lead to uncontrolled
 cellular growth and morphological changes. Cellular biomembranes are intimately involved in the regulation of cell signaling;
 however, they remain largely understudied. Phospholipids (PLs) are the main constituents of biological membranes and play
 important functional, structural and metabolic roles. The aim of this study was to establish if patterns in the PL profiles
 of mammary epithelial cells and breast cancer cells differ in relation to degree of differentiation and metastatic potential.
 For this purpose, PLs were analyzed using a lipidomic approach. In brief, PLs were extracted using Bligh and Dyer method,
 followed by a separa...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384613</comments>
            <pubDate>Sat, 29 Oct 2011 05:47:00 +0100</pubDate>
            <guid isPermaLink="false">5384613</guid>        </item>
        <item>
            <title>A systematic review of breast cancer incidence risk prediction models with meta-analysis of their performance</title>
            <link>http://www.medworm.com/index.php?rid=5384616&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8281w3xv514m148t%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A risk prediction model is a statistical tool for estimating the probability that a currently healthy individual with specific
 risk factors will develop a condition in the future such as breast cancer. Reliably accurate prediction models can inform
 future disease burdens, health policies and individual decisions. Breast cancer prediction models containing modifiable risk
 factors, such as alcohol consumption, BMI or weight, condom use, exogenous hormone use and physical activity, are of particular
 interest to women who might be considering how to reduce their risk of breast cancer and clinicians developing health policies
 to reduce population incidence rates. We performed a systematic review to identify and evaluate the performance of prediction
 models for breast c...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384616</comments>
            <pubDate>Sat, 29 Oct 2011 05:46:59 +0100</pubDate>
            <guid isPermaLink="false">5384616</guid>        </item>
        <item>
            <title>Predictive value of neoadjuvant chemotherapy failure in breast cancer using FDG–PET after the first course</title>
            <link>http://www.medworm.com/index.php?rid=5384615&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F0177632756723r41%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The aim of this study was to prospectively evaluate the predictive value of 18F-fluorodeoxyglucose–positron emission tomography (FDG–PET) to detect the absence of pathological response to preoperative
 chemotherapy in patients (pts) with breast cancer. 63 consecutive pts with non-metastatic, non-inflammatory breast cancer,
 eligible for neoadjuvant chemotherapy (3 FEC 100 followed by 3 Docetaxel) were enrolled. FDG–PET was performed just before
 the first as well as before the second course. Metabolic activity (tumour FDG uptake) was measured by standardised uptake
 value (SUVmax). Pts were classified as non-responders (NR) when the decrease of SUVmax in the primary tumour was less than 15% at the time of the second PET (EORTC 1999 criteria). The metabolic respons...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384615</comments>
            <pubDate>Sat, 29 Oct 2011 05:46:59 +0100</pubDate>
            <guid isPermaLink="false">5384615</guid>        </item>
        <item>
            <title>Folate intake and breast cancer mortality in a cohort of Swedish women</title>
            <link>http://www.medworm.com/index.php?rid=5384617&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp62g1628914426n1%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Folate may influence breast cancer development and progression through its role in one-carbon metabolism. However, epidemiologic
 data on the relation between folate and breast cancer survival are limited. We investigated whether dietary folate intake
 was associated with survival in 3,116 women diagnosed with breast cancer in the population-based Swedish Mammography Cohort.
 Participants completed a 67-item food frequency questionnaire in 1987. Cox proportional hazard models were used to calculate
 hazard ratios (HRs) and 95% confidence intervals (95% CIs) for death from breast cancer and death from any cause. During 25,716
 person-years of follow-up from 1987 to 2008, there were 852 deaths with 381 breast cancer deaths. Dietary folate intake was
 inversely associated ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384617</comments>
            <pubDate>Sat, 29 Oct 2011 05:46:58 +0100</pubDate>
            <guid isPermaLink="false">5384617</guid>        </item>
        <item>
            <title>The postmenopausal hormone replacement therapy-related breast cancer risk is decreased in women carrying the CYP2C19*17 variant</title>
            <link>http://www.medworm.com/index.php?rid=5384618&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn58v401708t4r026%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-4DOI 10.1007/s10549-011-1827-1Authors
		Christina Justenhoven, Dr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology, Stuttgart, GermanyOfure Obazee, Dr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology, Stuttgart, GermanyStefan Winter, Dr. Margarete Fischer-Bosch-Institute of Clinical Pharmacology, Stuttgart, GermanyFergus J. Couch, Departments of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USAJanet E. Olson, Departments of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USAPer Hall, Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockholm, SwedenUlf Hannelius, Department of Medical Epidemiology and Biostatistics, Karolinska Institute, Stockh...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384618</comments>
            <pubDate>Sat, 29 Oct 2011 05:46:55 +0100</pubDate>
            <guid isPermaLink="false">5384618</guid>        </item>
        <item>
            <title>Prognostic impact of polymorphisms in the MYBL2 interacting genes in breast cancer</title>
            <link>http://www.medworm.com/index.php?rid=5384619&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw82n32np3v062221%2F</link>
            <description>In conclusion, our study suggests a role of genetic variation in BIRC5, BCL2
 and CLU as progression and prognostic markers for BC, supporting previous studies based on the expression of the genes.
 
 
	Content Type Journal ArticleCategory EpidemiologyPages 1-9DOI 10.1007/s10549-011-1826-2Authors
		Hong Shi, Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, 69120 Heidelberg, GermanyMelanie Bevier, Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 580, 69120 Heidelberg, GermanyRobert Johansson, Department of Radiation Science, Oncology, Umeå University, Umeå, SwedenKerstin Enquist-Olsson, Department of Public Health and Clinical Medicine/Nutritional Research, Umeå University, Ume...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5384619</comments>
            <pubDate>Sat, 29 Oct 2011 05:46:54 +0100</pubDate>
            <guid isPermaLink="false">5384619</guid>        </item>
        <item>
            <title>Resolution of extensive leptomeningeal metastasis and clinical spinal cord compression from breast cancer using weekly docetaxel chemotherapy</title>
            <link>http://www.medworm.com/index.php?rid=5359968&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk863845788788124%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Metastatic breast cancer to the leptomeninges is a late event in the disease course and is associated with significant morbidity
 and a grave prognosis. Treatment typically involves direct intrathecal injection of chemotherapy into the cerebrospinal fluid
 compartment since systemic chemotherapy penetrates poorly to the central nervous system. Here we report an interesting clinical
 observation involving a patient presenting with leptomeningeal spread of breast cancer causing extensive spinal cord compression
 with obliteration of the subarachnoid space, thus precluding the use of direct intrathecal chemotherapy. We administered systemic
 chemotherapy using weekly docetaxel with complete radiographic resolution of her disease and recovery from clinical spinal
 cord comp...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5359968</comments>
            <pubDate>Fri, 28 Oct 2011 17:14:43 +0100</pubDate>
            <guid isPermaLink="false">5359968</guid>        </item>
        <item>
            <title>Life stage differences in mammary gland gene expression profile in non-human primates</title>
            <link>http://www.medworm.com/index.php?rid=5359967&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fuugr766072410250%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Breast cancer (BC) is the most common malignancy of women in the developed world. To better understand its pathogenesis, knowledge
 of normal breast development is crucial, as BC is the result of disregulation of physiologic processes. The aim of this study
 was to investigate the impact of reproductive life stages on the transcriptional profile of the mammary gland in a primate
 model. Comparative transcriptomic analyses were carried out using breast tissues from 28 female cynomolgus macaques (Macaca fascicularis) at the following life stages: prepubertal (n&amp;nbsp;=&amp;nbsp;5), adolescent (n&amp;nbsp;=&amp;nbsp;4), adult luteal (n&amp;nbsp;=&amp;nbsp;5), pregnant (n&amp;nbsp;=&amp;nbsp;6), lactating (n&amp;nbsp;=&amp;nbsp;3), and postmenopausal (n&amp;nbsp;=&amp;nbsp;5). Mammary gland RNA was hybridized to Affym...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5359967</comments>
            <pubDate>Fri, 28 Oct 2011 17:14:43 +0100</pubDate>
            <guid isPermaLink="false">5359967</guid>        </item>
        <item>
            <title>Clinician awareness and knowledge of breast cancer-related lymphedema in a large, integrated health care delivery setting</title>
            <link>http://www.medworm.com/index.php?rid=5359969&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F358w6n4q676h6wt8%2F</link>
            <description>We describe clinician knowledge and treatment referral of patients with BCRL among active oncologists,
 surgeons, and primary care physicians in the Kaiser Permanente Northern California Medical Care Program. A total of 887 oncologists,
 surgeons, and primary care clinicians completed a 10-minute web survey from May 2, 2010 to December 31, 2010 on BCRL knowledge,
 education, and referral patterns. A knowledge score of BCRL was calculated based on clinician responses. Multivariable regression
 models were used to determine the associations of selected covariates with BCRL knowledge score and clinician referral, respectively.
 Compared with primary care clinicians, oncologists had the highest mean score followed closely by surgeons (P&amp;nbsp;&amp;lt;&amp;nbsp;0.0001). In multivariable analyses, being ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5359969</comments>
            <pubDate>Fri, 28 Oct 2011 17:14:42 +0100</pubDate>
            <guid isPermaLink="false">5359969</guid>        </item>
        <item>
            <title>Variation in the risk of radiation-related contralateral breast cancer by histology and estrogen receptor expression in SEER</title>
            <link>http://www.medworm.com/index.php?rid=5346896&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu68l4343m0125045%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Radiation exposure, particularly at a young age, is an established cause of breast cancer. It is not known whether radiation-related
 breast cancer risk varies by molecular subtype. We characterized the relative risk (RR) of contralateral breast cancer (CBC)
 related to radiotherapy by histology and estrogen receptor (ER) status of the CBC in five-year survivors in the Surveillance,
 Epidemiology, and End Results database using Poisson regression models adjusted for attained age and calendar year, age at
 and year of treatment, ER status of the first breast cancer, and disease stage. 205,316 female breast cancer survivors were
 followed for an average of 10&amp;nbsp;years from 1973 until 2007, during which time 6924 women developed a subsequent primary invasive
 breast canc...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5346896</comments>
            <pubDate>Fri, 21 Oct 2011 06:10:32 +0100</pubDate>
            <guid isPermaLink="false">5346896</guid>        </item>
        <item>
            <title>GRB7 is required for triple-negative breast cancer cell invasion and survival</title>
            <link>http://www.medworm.com/index.php?rid=5335150&amp;cid=s_33460_6_f&amp;fid=33460&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F332hx6215163n484%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Triple-negative breast cancer (TNBC) is a heterogeneous disease that is usually associated with poor prognosis, and frequently
 associated with the basal-like breast cancer gene expression profile. There are no targeted therapeutic modalities for this
 disease, and no useful biomarkers. High GRB7 RNA expression levels are associated with an elevated risk of recurrence in patients with operable TNBC treated with standard
 adjuvant anthracycline and taxane therapy. To determine whether GRB7 is involved in the pathobiology of TNBC, we evaluated
 the biological effects of GRB7 inhibition in a panel of triple-negative cell lines—MDA-MB-468, MDA-MB-231, HCC70, and T4-2.
 We found GRB7 inhibition reduced cell motility and invasion of these cell lines and promoted cell death ...</description>
            <author>Breast Cancer Research and Treatment</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5335150</comments>
            <pubDate>Mon, 17 Oct 2011 16:00:57 +0100</pubDate>
            <guid isPermaLink="false">5335150</guid>        </item>
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