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Frequency of Androgen Receptor Positivity in Tumors: A Study Evaluating More Than 18,000 Tumors
Androgen receptor (AR) is a transcription factor expressed in various normal tissues and is a therapeutic target for prostate and possibly other cancers. A TMA containing 18,234 samples from 141 different tumor types/subtypes and 608 samples of 76 different normal tissue types was analyzed by immuno...
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Published in: | Biomedicines 2024-05, Vol.12 (5), p.957 |
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creator | Viehweger, Florian Hoop, Jennifer Tinger, Lisa-Marie Bernreuther, Christian Büscheck, Franziska Clauditz, Till S Hinsch, Andrea Jacobsen, Frank Luebke, Andreas M Steurer, Stefan Hube-Magg, Claudia Kluth, Martina Marx, Andreas H Krech, Till Lebok, Patrick Fraune, Christoph Burandt, Eike Sauter, Guido Simon, Ronald Minner, Sarah |
description | Androgen receptor (AR) is a transcription factor expressed in various normal tissues and is a therapeutic target for prostate and possibly other cancers. A TMA containing 18,234 samples from 141 different tumor types/subtypes and 608 samples of 76 different normal tissue types was analyzed by immunohistochemistry. AR positivity was found in 116 tumor types including 66 tumor types (46.8%) with ≥1 strongly positive tumor. Moderate/strong AR positivity was detected in testicular sex cord-stromal tumors (93.3-100%) and neoplasms of the prostate (79.3-98.7%), breast (25.0-75.5%), other gynecological tumors (0.9-100%), kidney (5.0-44.1%), and urinary bladder (5.4-24.2%). Low AR staining was associated with advanced tumor stage (pTa versus pT2-4;
< 0.0001) in urothelial carcinoma; advanced pT (
< 0.0001), high tumor grade (
< 0.0001), nodal metastasis (
< 0.0001), and reduced survival (
= 0.0024) in invasive breast carcinoma; high pT (
< 0.0001) and grade (
< 0.0001) in clear cell renal cell carcinoma (RCC); and high pT (
= 0.0055) as well as high grade (
< 0.05) in papillary RCC. AR staining was unrelated to histopathological/clinical features in 157 endometrial carcinomas and in 221 ovarian carcinomas. Our data suggest a limited role of AR immunohistochemistry for tumor distinction and a prognostic role in breast and clear cell RCC and highlight tumor entities that might benefit from AR-targeted therapy. |
doi_str_mv | 10.3390/biomedicines12050957 |
format | article |
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< 0.0001) in urothelial carcinoma; advanced pT (
< 0.0001), high tumor grade (
< 0.0001), nodal metastasis (
< 0.0001), and reduced survival (
= 0.0024) in invasive breast carcinoma; high pT (
< 0.0001) and grade (
< 0.0001) in clear cell renal cell carcinoma (RCC); and high pT (
= 0.0055) as well as high grade (
< 0.05) in papillary RCC. AR staining was unrelated to histopathological/clinical features in 157 endometrial carcinomas and in 221 ovarian carcinomas. Our data suggest a limited role of AR immunohistochemistry for tumor distinction and a prognostic role in breast and clear cell RCC and highlight tumor entities that might benefit from AR-targeted therapy.]]></description><identifier>ISSN: 2227-9059</identifier><identifier>EISSN: 2227-9059</identifier><identifier>DOI: 10.3390/biomedicines12050957</identifier><identifier>PMID: 38790919</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>androgen receptor ; Androgen receptors ; Androgens ; Antibodies ; Breast cancer ; Breast carcinoma ; Cancer ; Clear cell-type renal cell carcinoma ; Immunohistochemistry ; Medical prognosis ; Metastases ; Ovarian cancer ; Ovarian carcinoma ; Pathology ; Patients ; prognosis ; Prostate ; Prostate cancer ; Statistical analysis ; Therapeutic targets ; tissue microarray ; Tumors ; Urinary bladder ; Urothelial carcinoma ; Uterine cancer ; Uterus</subject><ispartof>Biomedicines, 2024-05, Vol.12 (5), p.957</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c393t-89ff2f8c7ab1839b06cd4cf08e5ec045710d4d923454009434ce55e49ba747b63</cites><orcidid>0000-0002-4257-856X ; 0000-0003-1464-6964 ; 0000-0003-3652-532X ; 0000-0003-0158-4258 ; 0000-0001-7542-4340</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3059405822/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3059405822?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,25731,27901,27902,36989,36990,44566,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38790919$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Viehweger, Florian</creatorcontrib><creatorcontrib>Hoop, Jennifer</creatorcontrib><creatorcontrib>Tinger, Lisa-Marie</creatorcontrib><creatorcontrib>Bernreuther, Christian</creatorcontrib><creatorcontrib>Büscheck, Franziska</creatorcontrib><creatorcontrib>Clauditz, Till S</creatorcontrib><creatorcontrib>Hinsch, Andrea</creatorcontrib><creatorcontrib>Jacobsen, Frank</creatorcontrib><creatorcontrib>Luebke, Andreas M</creatorcontrib><creatorcontrib>Steurer, Stefan</creatorcontrib><creatorcontrib>Hube-Magg, Claudia</creatorcontrib><creatorcontrib>Kluth, Martina</creatorcontrib><creatorcontrib>Marx, Andreas H</creatorcontrib><creatorcontrib>Krech, Till</creatorcontrib><creatorcontrib>Lebok, Patrick</creatorcontrib><creatorcontrib>Fraune, Christoph</creatorcontrib><creatorcontrib>Burandt, Eike</creatorcontrib><creatorcontrib>Sauter, Guido</creatorcontrib><creatorcontrib>Simon, Ronald</creatorcontrib><creatorcontrib>Minner, Sarah</creatorcontrib><title>Frequency of Androgen Receptor Positivity in Tumors: A Study Evaluating More Than 18,000 Tumors</title><title>Biomedicines</title><addtitle>Biomedicines</addtitle><description><![CDATA[Androgen receptor (AR) is a transcription factor expressed in various normal tissues and is a therapeutic target for prostate and possibly other cancers. A TMA containing 18,234 samples from 141 different tumor types/subtypes and 608 samples of 76 different normal tissue types was analyzed by immunohistochemistry. AR positivity was found in 116 tumor types including 66 tumor types (46.8%) with ≥1 strongly positive tumor. Moderate/strong AR positivity was detected in testicular sex cord-stromal tumors (93.3-100%) and neoplasms of the prostate (79.3-98.7%), breast (25.0-75.5%), other gynecological tumors (0.9-100%), kidney (5.0-44.1%), and urinary bladder (5.4-24.2%). Low AR staining was associated with advanced tumor stage (pTa versus pT2-4;
< 0.0001) in urothelial carcinoma; advanced pT (
< 0.0001), high tumor grade (
< 0.0001), nodal metastasis (
< 0.0001), and reduced survival (
= 0.0024) in invasive breast carcinoma; high pT (
< 0.0001) and grade (
< 0.0001) in clear cell renal cell carcinoma (RCC); and high pT (
= 0.0055) as well as high grade (
< 0.05) in papillary RCC. AR staining was unrelated to histopathological/clinical features in 157 endometrial carcinomas and in 221 ovarian carcinomas. Our data suggest a limited role of AR immunohistochemistry for tumor distinction and a prognostic role in breast and clear cell RCC and highlight tumor entities that might benefit from AR-targeted therapy.]]></description><subject>androgen receptor</subject><subject>Androgen receptors</subject><subject>Androgens</subject><subject>Antibodies</subject><subject>Breast cancer</subject><subject>Breast carcinoma</subject><subject>Cancer</subject><subject>Clear cell-type renal cell carcinoma</subject><subject>Immunohistochemistry</subject><subject>Medical prognosis</subject><subject>Metastases</subject><subject>Ovarian cancer</subject><subject>Ovarian carcinoma</subject><subject>Pathology</subject><subject>Patients</subject><subject>prognosis</subject><subject>Prostate</subject><subject>Prostate cancer</subject><subject>Statistical analysis</subject><subject>Therapeutic targets</subject><subject>tissue microarray</subject><subject>Tumors</subject><subject>Urinary bladder</subject><subject>Urothelial carcinoma</subject><subject>Uterine cancer</subject><subject>Uterus</subject><issn>2227-9059</issn><issn>2227-9059</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkl1vFCEUhidGY5vaf2AMiTdedCszfHu3aVrbpEaj6zVh4MzKZgZWYJrsv5e62_qRwgVfz_seDpymed3ic0IUft_7OIHz1gfIbYcZVkw8a467rhMLhZl6_tf8qDnNeYNrUy2RLX3ZHBEpVF2p40ZfJfg5Q7A7FAe0DC7FNQT0FSxsS0zoS8y--DtfdsgHtJqnmPIHtETfyux26PLOjLMpPqzRp5gArX6YgFp5VmMd2FfNi8GMGU4P40nz_epydXG9uP388eZiebuwRJGykGoYukFaYfpWEtVjbh21A5bAwGLKRIsddaojlNGaByXUAmNAVW8EFT0nJ83N3tdFs9Hb5CeTdjoar39vxLTWJhVvR9BcUM6t5CB7RRVlxvacU9WBsc7hFqrXu73XNsX6NrnoyWcL42gCxDlrgjkmggiKK_r2P3QT5xRqppViimImu-4PtTY1vg9DLMnYe1O9FIrVT-FMVur8Cap2B5O3McDg6_4_AroX2BRzTjA85t1ifV8m-qkyqbI3hzvPfT19FD0UBfkFYGW3jA</recordid><startdate>20240501</startdate><enddate>20240501</enddate><creator>Viehweger, Florian</creator><creator>Hoop, Jennifer</creator><creator>Tinger, Lisa-Marie</creator><creator>Bernreuther, Christian</creator><creator>Büscheck, Franziska</creator><creator>Clauditz, Till S</creator><creator>Hinsch, Andrea</creator><creator>Jacobsen, Frank</creator><creator>Luebke, Andreas M</creator><creator>Steurer, Stefan</creator><creator>Hube-Magg, Claudia</creator><creator>Kluth, Martina</creator><creator>Marx, Andreas H</creator><creator>Krech, Till</creator><creator>Lebok, Patrick</creator><creator>Fraune, Christoph</creator><creator>Burandt, Eike</creator><creator>Sauter, Guido</creator><creator>Simon, Ronald</creator><creator>Minner, Sarah</creator><general>MDPI AG</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</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>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-4257-856X</orcidid><orcidid>https://orcid.org/0000-0003-1464-6964</orcidid><orcidid>https://orcid.org/0000-0003-3652-532X</orcidid><orcidid>https://orcid.org/0000-0003-0158-4258</orcidid><orcidid>https://orcid.org/0000-0001-7542-4340</orcidid></search><sort><creationdate>20240501</creationdate><title>Frequency of Androgen Receptor Positivity in Tumors: A Study Evaluating More Than 18,000 Tumors</title><author>Viehweger, Florian ; Hoop, Jennifer ; Tinger, Lisa-Marie ; Bernreuther, Christian ; Büscheck, Franziska ; Clauditz, Till S ; Hinsch, Andrea ; Jacobsen, Frank ; Luebke, Andreas M ; Steurer, Stefan ; Hube-Magg, Claudia ; Kluth, Martina ; Marx, Andreas H ; Krech, Till ; Lebok, Patrick ; Fraune, Christoph ; Burandt, Eike ; Sauter, Guido ; Simon, Ronald ; Minner, Sarah</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-89ff2f8c7ab1839b06cd4cf08e5ec045710d4d923454009434ce55e49ba747b63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>androgen receptor</topic><topic>Androgen receptors</topic><topic>Androgens</topic><topic>Antibodies</topic><topic>Breast cancer</topic><topic>Breast carcinoma</topic><topic>Cancer</topic><topic>Clear cell-type renal cell carcinoma</topic><topic>Immunohistochemistry</topic><topic>Medical prognosis</topic><topic>Metastases</topic><topic>Ovarian cancer</topic><topic>Ovarian carcinoma</topic><topic>Pathology</topic><topic>Patients</topic><topic>prognosis</topic><topic>Prostate</topic><topic>Prostate cancer</topic><topic>Statistical analysis</topic><topic>Therapeutic targets</topic><topic>tissue microarray</topic><topic>Tumors</topic><topic>Urinary bladder</topic><topic>Urothelial carcinoma</topic><topic>Uterine cancer</topic><topic>Uterus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Viehweger, Florian</creatorcontrib><creatorcontrib>Hoop, Jennifer</creatorcontrib><creatorcontrib>Tinger, Lisa-Marie</creatorcontrib><creatorcontrib>Bernreuther, Christian</creatorcontrib><creatorcontrib>Büscheck, Franziska</creatorcontrib><creatorcontrib>Clauditz, Till S</creatorcontrib><creatorcontrib>Hinsch, Andrea</creatorcontrib><creatorcontrib>Jacobsen, Frank</creatorcontrib><creatorcontrib>Luebke, Andreas M</creatorcontrib><creatorcontrib>Steurer, Stefan</creatorcontrib><creatorcontrib>Hube-Magg, Claudia</creatorcontrib><creatorcontrib>Kluth, Martina</creatorcontrib><creatorcontrib>Marx, Andreas H</creatorcontrib><creatorcontrib>Krech, Till</creatorcontrib><creatorcontrib>Lebok, Patrick</creatorcontrib><creatorcontrib>Fraune, Christoph</creatorcontrib><creatorcontrib>Burandt, Eike</creatorcontrib><creatorcontrib>Sauter, Guido</creatorcontrib><creatorcontrib>Simon, Ronald</creatorcontrib><creatorcontrib>Minner, Sarah</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Biological Sciences</collection><collection>Biological Science Database</collection><collection>Publicly Available Content (ProQuest)</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 China</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Biomedicines</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Viehweger, Florian</au><au>Hoop, Jennifer</au><au>Tinger, Lisa-Marie</au><au>Bernreuther, Christian</au><au>Büscheck, Franziska</au><au>Clauditz, Till S</au><au>Hinsch, Andrea</au><au>Jacobsen, Frank</au><au>Luebke, Andreas M</au><au>Steurer, Stefan</au><au>Hube-Magg, Claudia</au><au>Kluth, Martina</au><au>Marx, Andreas H</au><au>Krech, Till</au><au>Lebok, Patrick</au><au>Fraune, Christoph</au><au>Burandt, Eike</au><au>Sauter, Guido</au><au>Simon, Ronald</au><au>Minner, Sarah</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Frequency of Androgen Receptor Positivity in Tumors: A Study Evaluating More Than 18,000 Tumors</atitle><jtitle>Biomedicines</jtitle><addtitle>Biomedicines</addtitle><date>2024-05-01</date><risdate>2024</risdate><volume>12</volume><issue>5</issue><spage>957</spage><pages>957-</pages><issn>2227-9059</issn><eissn>2227-9059</eissn><abstract><![CDATA[Androgen receptor (AR) is a transcription factor expressed in various normal tissues and is a therapeutic target for prostate and possibly other cancers. A TMA containing 18,234 samples from 141 different tumor types/subtypes and 608 samples of 76 different normal tissue types was analyzed by immunohistochemistry. AR positivity was found in 116 tumor types including 66 tumor types (46.8%) with ≥1 strongly positive tumor. Moderate/strong AR positivity was detected in testicular sex cord-stromal tumors (93.3-100%) and neoplasms of the prostate (79.3-98.7%), breast (25.0-75.5%), other gynecological tumors (0.9-100%), kidney (5.0-44.1%), and urinary bladder (5.4-24.2%). Low AR staining was associated with advanced tumor stage (pTa versus pT2-4;
< 0.0001) in urothelial carcinoma; advanced pT (
< 0.0001), high tumor grade (
< 0.0001), nodal metastasis (
< 0.0001), and reduced survival (
= 0.0024) in invasive breast carcinoma; high pT (
< 0.0001) and grade (
< 0.0001) in clear cell renal cell carcinoma (RCC); and high pT (
= 0.0055) as well as high grade (
< 0.05) in papillary RCC. AR staining was unrelated to histopathological/clinical features in 157 endometrial carcinomas and in 221 ovarian carcinomas. Our data suggest a limited role of AR immunohistochemistry for tumor distinction and a prognostic role in breast and clear cell RCC and highlight tumor entities that might benefit from AR-targeted therapy.]]></abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>38790919</pmid><doi>10.3390/biomedicines12050957</doi><orcidid>https://orcid.org/0000-0002-4257-856X</orcidid><orcidid>https://orcid.org/0000-0003-1464-6964</orcidid><orcidid>https://orcid.org/0000-0003-3652-532X</orcidid><orcidid>https://orcid.org/0000-0003-0158-4258</orcidid><orcidid>https://orcid.org/0000-0001-7542-4340</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | androgen receptor Androgen receptors Androgens Antibodies Breast cancer Breast carcinoma Cancer Clear cell-type renal cell carcinoma Immunohistochemistry Medical prognosis Metastases Ovarian cancer Ovarian carcinoma Pathology Patients prognosis Prostate Prostate cancer Statistical analysis Therapeutic targets tissue microarray Tumors Urinary bladder Urothelial carcinoma Uterine cancer Uterus |
title | Frequency of Androgen Receptor Positivity in Tumors: A Study Evaluating More Than 18,000 Tumors |
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