A targetable androgen receptor-positive breast cancer subtype hidden among the triple-negative cancers
Triple-negative breast cancer (TNBC) is a subgroup of breast cancers that by definition lack expression of estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 (HER2). A diverse group of tumors, TNBC shares some morphologic and molecular features with basal-like bre...
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Veröffentlicht in: | Archives of pathology & laboratory medicine (1976) 2015-05, Vol.139 (5), p.612-617 |
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description | Triple-negative breast cancer (TNBC) is a subgroup of breast cancers that by definition lack expression of estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 (HER2). A diverse group of tumors, TNBC shares some morphologic and molecular features with basal-like breast cancer, a category of breast cancer defined by gene expression profiling. More likely to occur in young women and African Americans, TNBCs may exhibit aggressive behavior and are associated with poor prognosis despite their initial response to conventional chemotherapy. Because hormonal or HER2-targeted therapies are ineffective for these tumors, the main therapeutic option is systemic chemotherapy. Therefore, identification of new targets for therapy is urgently needed for this group.
To review and present recent literature along with our own experience regarding the clinical and morphologic characteristics and the prevalence of androgen receptor (AR) expression in TNBC, and to discuss the potential use of AR as a therapeutic target for AR(+) TNBC.
Data sources are published articles from peer-reviewed journals in PubMed (US National Library of Medicine).
AR is the most commonly expressed hormone receptor among all breast carcinomas, with a prevalence of 25% to 75% among TNBCs. Therefore, we strongly support the routine assessment of AR in TNBC, and preferably in all breast carcinomas. |
doi_str_mv | 10.5858/arpa.2014-0122-RA |
format | Article |
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To review and present recent literature along with our own experience regarding the clinical and morphologic characteristics and the prevalence of androgen receptor (AR) expression in TNBC, and to discuss the potential use of AR as a therapeutic target for AR(+) TNBC.
Data sources are published articles from peer-reviewed journals in PubMed (US National Library of Medicine).
AR is the most commonly expressed hormone receptor among all breast carcinomas, with a prevalence of 25% to 75% among TNBCs. Therefore, we strongly support the routine assessment of AR in TNBC, and preferably in all breast carcinomas.</description><identifier>ISSN: 0003-9985</identifier><identifier>ISSN: 1543-2165</identifier><identifier>EISSN: 1543-2165</identifier><identifier>DOI: 10.5858/arpa.2014-0122-RA</identifier><identifier>PMID: 25310144</identifier><identifier>CODEN: APLMAS</identifier><language>eng</language><publisher>United States: College of American Pathologists</publisher><subject>African Americans ; Biomarkers, Tumor - genetics ; Biomarkers, Tumor - metabolism ; Breast cancer ; Breast Neoplasms - pathology ; Breast Neoplasms - therapy ; Cancer genetics ; Care and treatment ; Chemotherapy ; Development and progression ; Epidermal growth factors ; Estrogens ; Female ; Gene expression ; Genes ; Genetic aspects ; Humans ; Progesterone ; Prognosis ; Receptors, Androgen - genetics ; Receptors, Androgen - metabolism ; Triple Negative Breast Neoplasms - pathology ; Triple Negative Breast Neoplasms - therapy</subject><ispartof>Archives of pathology & laboratory medicine (1976), 2015-05, Vol.139 (5), p.612-617</ispartof><rights>COPYRIGHT 2015 College of American Pathologists</rights><rights>Copyright College of American Pathologists May 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c531t-3a4f01b5641c4feb54b1d11edc8a079173843604a4a45a7d3888fcd51a512f793</citedby><cites>FETCH-LOGICAL-c531t-3a4f01b5641c4feb54b1d11edc8a079173843604a4a45a7d3888fcd51a512f793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25310144$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Safarpour, Damoun</creatorcontrib><creatorcontrib>Tavassoli, Fattaneh A</creatorcontrib><title>A targetable androgen receptor-positive breast cancer subtype hidden among the triple-negative cancers</title><title>Archives of pathology & laboratory medicine (1976)</title><addtitle>Arch Pathol Lab Med</addtitle><description>Triple-negative breast cancer (TNBC) is a subgroup of breast cancers that by definition lack expression of estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 (HER2). A diverse group of tumors, TNBC shares some morphologic and molecular features with basal-like breast cancer, a category of breast cancer defined by gene expression profiling. More likely to occur in young women and African Americans, TNBCs may exhibit aggressive behavior and are associated with poor prognosis despite their initial response to conventional chemotherapy. Because hormonal or HER2-targeted therapies are ineffective for these tumors, the main therapeutic option is systemic chemotherapy. Therefore, identification of new targets for therapy is urgently needed for this group.
To review and present recent literature along with our own experience regarding the clinical and morphologic characteristics and the prevalence of androgen receptor (AR) expression in TNBC, and to discuss the potential use of AR as a therapeutic target for AR(+) TNBC.
Data sources are published articles from peer-reviewed journals in PubMed (US National Library of Medicine).
AR is the most commonly expressed hormone receptor among all breast carcinomas, with a prevalence of 25% to 75% among TNBCs. Therefore, we strongly support the routine assessment of AR in TNBC, and preferably in all breast carcinomas.</description><subject>African Americans</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - pathology</subject><subject>Breast Neoplasms - therapy</subject><subject>Cancer genetics</subject><subject>Care and treatment</subject><subject>Chemotherapy</subject><subject>Development and progression</subject><subject>Epidermal growth factors</subject><subject>Estrogens</subject><subject>Female</subject><subject>Gene expression</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Humans</subject><subject>Progesterone</subject><subject>Prognosis</subject><subject>Receptors, Androgen - genetics</subject><subject>Receptors, Androgen - metabolism</subject><subject>Triple Negative Breast Neoplasms - pathology</subject><subject>Triple Negative Breast Neoplasms - therapy</subject><issn>0003-9985</issn><issn>1543-2165</issn><issn>1543-2165</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNptkl2L1TAQhoso7nH1B3gjBUG8yTHTJG16eVj8ggVh0eswTac9XdqmJqmw_97Us36sHOYiZHieYRjeLHsJfK-00u_QL7gvOEjGoSjYzeFRtgMlBSugVI-zHedcsLrW6iJ7FsJt-tZFAU-zi0IJSJrcZd0hj-h7itiMlOPcetfTnHuytETn2eLCEIcflDeeMMTc4mzJ52Ft4t1C-XFo24Tj5OY-j0fKox-WkdhMPf7STnx4nj3pcAz04v69zL59eP_16hO7_vLx89Xhmtm0UWQCZcehUaUEKztqlGygBaDWauRVDZXQUpRcYiqFVSu01p1tFaCCoqtqcZm9Pc1dvPu-UohmGoKlccSZ3BoMlFWlawF1mdDX_6G3bvVz2m6jal1JCcVfqseRzDB3Lnq021BzUMBrUUFdJYqdodIhyePoZuqG1H7A78_wqVqaBntWePOPcCQc4zG4cY2Dm8NDEE6g9S4ET51Z_DChvzPAzRYas4XGbKExW2jMzSE5r-4vsTYTtX-M3ykRPwGvM7th</recordid><startdate>20150501</startdate><enddate>20150501</enddate><creator>Safarpour, Damoun</creator><creator>Tavassoli, Fattaneh A</creator><general>College of American Pathologists</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20150501</creationdate><title>A targetable androgen receptor-positive breast cancer subtype hidden among the triple-negative cancers</title><author>Safarpour, Damoun ; Tavassoli, Fattaneh A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c531t-3a4f01b5641c4feb54b1d11edc8a079173843604a4a45a7d3888fcd51a512f793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>African Americans</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - pathology</topic><topic>Breast Neoplasms - therapy</topic><topic>Cancer genetics</topic><topic>Care and treatment</topic><topic>Chemotherapy</topic><topic>Development and progression</topic><topic>Epidermal growth factors</topic><topic>Estrogens</topic><topic>Female</topic><topic>Gene expression</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Humans</topic><topic>Progesterone</topic><topic>Prognosis</topic><topic>Receptors, Androgen - genetics</topic><topic>Receptors, Androgen - metabolism</topic><topic>Triple Negative Breast Neoplasms - pathology</topic><topic>Triple Negative Breast Neoplasms - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Safarpour, Damoun</creatorcontrib><creatorcontrib>Tavassoli, Fattaneh A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of pathology & laboratory medicine (1976)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Safarpour, Damoun</au><au>Tavassoli, Fattaneh A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A targetable androgen receptor-positive breast cancer subtype hidden among the triple-negative cancers</atitle><jtitle>Archives of pathology & laboratory medicine (1976)</jtitle><addtitle>Arch Pathol Lab Med</addtitle><date>2015-05-01</date><risdate>2015</risdate><volume>139</volume><issue>5</issue><spage>612</spage><epage>617</epage><pages>612-617</pages><issn>0003-9985</issn><issn>1543-2165</issn><eissn>1543-2165</eissn><coden>APLMAS</coden><abstract>Triple-negative breast cancer (TNBC) is a subgroup of breast cancers that by definition lack expression of estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 (HER2). A diverse group of tumors, TNBC shares some morphologic and molecular features with basal-like breast cancer, a category of breast cancer defined by gene expression profiling. More likely to occur in young women and African Americans, TNBCs may exhibit aggressive behavior and are associated with poor prognosis despite their initial response to conventional chemotherapy. Because hormonal or HER2-targeted therapies are ineffective for these tumors, the main therapeutic option is systemic chemotherapy. Therefore, identification of new targets for therapy is urgently needed for this group.
To review and present recent literature along with our own experience regarding the clinical and morphologic characteristics and the prevalence of androgen receptor (AR) expression in TNBC, and to discuss the potential use of AR as a therapeutic target for AR(+) TNBC.
Data sources are published articles from peer-reviewed journals in PubMed (US National Library of Medicine).
AR is the most commonly expressed hormone receptor among all breast carcinomas, with a prevalence of 25% to 75% among TNBCs. Therefore, we strongly support the routine assessment of AR in TNBC, and preferably in all breast carcinomas.</abstract><cop>United States</cop><pub>College of American Pathologists</pub><pmid>25310144</pmid><doi>10.5858/arpa.2014-0122-RA</doi><tpages>6</tpages></addata></record> |
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source | MEDLINE; Allen Press Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | African Americans Biomarkers, Tumor - genetics Biomarkers, Tumor - metabolism Breast cancer Breast Neoplasms - pathology Breast Neoplasms - therapy Cancer genetics Care and treatment Chemotherapy Development and progression Epidermal growth factors Estrogens Female Gene expression Genes Genetic aspects Humans Progesterone Prognosis Receptors, Androgen - genetics Receptors, Androgen - metabolism Triple Negative Breast Neoplasms - pathology Triple Negative Breast Neoplasms - therapy |
title | A targetable androgen receptor-positive breast cancer subtype hidden among the triple-negative cancers |
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