Differences in Frequency of ERG Oncoprotein Expression Between Index Tumors of Caucasian and African American Patients With Prostate Cancer
Objective To systematically evaluate the ETS-related gene (ERG) alterations in the multifocal tumor context using whole-mount prostatectomy specimens from African and Caucasian American patients matched for age, pathologic grade and stage. Oncogenic activation of the ERG is the most common early gen...
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Veröffentlicht in: | Urology (Ridgewood, N.J.) N.J.), 2012-10, Vol.80 (4), p.749-753 |
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creator | Rosen, Philip Pfister, David Young, Denise Petrovics, Gyorgy Chen, Yongmei Cullen, Jennifer Böhm, Diana Perner, Sven Dobi, Albert McLeod, David G Sesterhenn, Isabell A Srivastava, Shiv |
description | Objective To systematically evaluate the ETS-related gene (ERG) alterations in the multifocal tumor context using whole-mount prostatectomy specimens from African and Caucasian American patients matched for age, pathologic grade and stage. Oncogenic activation of the ERG is the most common early genomic alteration in patients with prostate cancer (CaP) in Western countries. However, ERG alterations have not been systematically examined in African American patients with a known greater risk of CaP incidence and mortality. Methods ERG oncoprotein expression was analyzed in 91 Caucasian and 91 African American patients with CaP, who were matched for age, Gleason score, and pathologic stage. A unique aspect of the present study was the evaluation of ERG in whole-mount prostatectomy sections, minimizing sampling bias and allowing the careful assessment of the ERG in the multifocal tumor context of CaP. Results The frequency of ERG-positive prostate tumors was significantly greater among Caucasian Americans than among African Americans when assessed in all tumor foci (41.9% vs 23.9%, P < .0001). A markedly greater frequency of ERG oncoprotein expression was noted between the index tumors of the Caucasian Americans (63.3%) and those of the African Americans (28.6%). Also, in the African American patients, the higher grade index tumors were predominantly ERG negative. Conclusion ERG typing of CaP established a major difference between the index tumors of Caucasian and African American patients. ERG-negative index tumors might indicate a less favorable outcome for African American patients. The results of the present study underscore that typing of CaP for the ERG could enhance our understanding of the biologic differences between the examined ethnic groups. |
doi_str_mv | 10.1016/j.urology.2012.07.001 |
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Oncogenic activation of the ERG is the most common early genomic alteration in patients with prostate cancer (CaP) in Western countries. However, ERG alterations have not been systematically examined in African American patients with a known greater risk of CaP incidence and mortality. Methods ERG oncoprotein expression was analyzed in 91 Caucasian and 91 African American patients with CaP, who were matched for age, Gleason score, and pathologic stage. A unique aspect of the present study was the evaluation of ERG in whole-mount prostatectomy sections, minimizing sampling bias and allowing the careful assessment of the ERG in the multifocal tumor context of CaP. Results The frequency of ERG-positive prostate tumors was significantly greater among Caucasian Americans than among African Americans when assessed in all tumor foci (41.9% vs 23.9%, P < .0001). A markedly greater frequency of ERG oncoprotein expression was noted between the index tumors of the Caucasian Americans (63.3%) and those of the African Americans (28.6%). Also, in the African American patients, the higher grade index tumors were predominantly ERG negative. Conclusion ERG typing of CaP established a major difference between the index tumors of Caucasian and African American patients. ERG-negative index tumors might indicate a less favorable outcome for African American patients. The results of the present study underscore that typing of CaP for the ERG could enhance our understanding of the biologic differences between the examined ethnic groups.</description><identifier>ISSN: 0090-4295</identifier><identifier>EISSN: 1527-9995</identifier><identifier>DOI: 10.1016/j.urology.2012.07.001</identifier><identifier>PMID: 22950997</identifier><identifier>CODEN: URGYAZ</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>African Americans - genetics ; Aged ; Biological and medical sciences ; Carcinoma - genetics ; Carcinoma - metabolism ; Carcinoma - pathology ; European Continental Ancestry Group - genetics ; Gynecology. Andrology. Obstetrics ; Humans ; Kaplan-Meier Estimate ; Male ; Male genital diseases ; Medical sciences ; Middle Aged ; Nephrology. Urinary tract diseases ; Prostatic Neoplasms - genetics ; Prostatic Neoplasms - metabolism ; Prostatic Neoplasms - pathology ; Trans-Activators - genetics ; Trans-Activators - metabolism ; Transcriptional Regulator ERG ; Tumors ; Tumors of the urinary system ; Urinary tract. Prostate gland ; Urology</subject><ispartof>Urology (Ridgewood, N.J.), 2012-10, Vol.80 (4), p.749-753</ispartof><rights>Elsevier Inc.</rights><rights>2012 Elsevier Inc.</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c497t-b873bfeb593d58268f2a83f8dabc04e67c9bab71cba36fa7bc719126b28587e93</citedby><cites>FETCH-LOGICAL-c497t-b873bfeb593d58268f2a83f8dabc04e67c9bab71cba36fa7bc719126b28587e93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0090429512007674$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26701105$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22950997$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rosen, Philip</creatorcontrib><creatorcontrib>Pfister, David</creatorcontrib><creatorcontrib>Young, Denise</creatorcontrib><creatorcontrib>Petrovics, Gyorgy</creatorcontrib><creatorcontrib>Chen, Yongmei</creatorcontrib><creatorcontrib>Cullen, Jennifer</creatorcontrib><creatorcontrib>Böhm, Diana</creatorcontrib><creatorcontrib>Perner, Sven</creatorcontrib><creatorcontrib>Dobi, Albert</creatorcontrib><creatorcontrib>McLeod, David G</creatorcontrib><creatorcontrib>Sesterhenn, Isabell A</creatorcontrib><creatorcontrib>Srivastava, Shiv</creatorcontrib><title>Differences in Frequency of ERG Oncoprotein Expression Between Index Tumors of Caucasian and African American Patients With Prostate Cancer</title><title>Urology (Ridgewood, N.J.)</title><addtitle>Urology</addtitle><description>Objective To systematically evaluate the ETS-related gene (ERG) alterations in the multifocal tumor context using whole-mount prostatectomy specimens from African and Caucasian American patients matched for age, pathologic grade and stage. Oncogenic activation of the ERG is the most common early genomic alteration in patients with prostate cancer (CaP) in Western countries. However, ERG alterations have not been systematically examined in African American patients with a known greater risk of CaP incidence and mortality. Methods ERG oncoprotein expression was analyzed in 91 Caucasian and 91 African American patients with CaP, who were matched for age, Gleason score, and pathologic stage. A unique aspect of the present study was the evaluation of ERG in whole-mount prostatectomy sections, minimizing sampling bias and allowing the careful assessment of the ERG in the multifocal tumor context of CaP. Results The frequency of ERG-positive prostate tumors was significantly greater among Caucasian Americans than among African Americans when assessed in all tumor foci (41.9% vs 23.9%, P < .0001). A markedly greater frequency of ERG oncoprotein expression was noted between the index tumors of the Caucasian Americans (63.3%) and those of the African Americans (28.6%). Also, in the African American patients, the higher grade index tumors were predominantly ERG negative. Conclusion ERG typing of CaP established a major difference between the index tumors of Caucasian and African American patients. ERG-negative index tumors might indicate a less favorable outcome for African American patients. The results of the present study underscore that typing of CaP for the ERG could enhance our understanding of the biologic differences between the examined ethnic groups.</description><subject>African Americans - genetics</subject><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Carcinoma - genetics</subject><subject>Carcinoma - metabolism</subject><subject>Carcinoma - pathology</subject><subject>European Continental Ancestry Group - genetics</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Male</subject><subject>Male genital diseases</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Prostatic Neoplasms - metabolism</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Trans-Activators - genetics</subject><subject>Trans-Activators - metabolism</subject><subject>Transcriptional Regulator ERG</subject><subject>Tumors</subject><subject>Tumors of the urinary system</subject><subject>Urinary tract. Prostate gland</subject><subject>Urology</subject><issn>0090-4295</issn><issn>1527-9995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUstu1DAUjRCIDoVPAHmDxCbBdiZxvAENw7RUqtQKilhatnMNHhJ7sB3a-Yb-NI5mAIkNK1_b59zHObconhNcEUza19tqCn7wX_cVxYRWmFUYkwfFgjSUlZzz5mGxwJjjckl5c1I8iXGLMW7blj0uTmh-w5yzRXH_3hoDAZyGiKxDZwF-TPm2R96gzcdzdOW03wWfIH9u7nYBYrTeoXeQbgEcunA93KGbafQhzpS1nLSMVjokXY9WJlid49UIh-BaJgsuRfTFpm_oOviYZILMyvXD0-KRkUOEZ8fztPh8trlZfygvr84v1qvLUi85S6XqWK0MqIbXfdPRtjNUdrXpeqk0XkLLNFdSMaKVrFsjmdKMcEJbRbumY8Dr0-LVIW-eKw8bkxht1DAM0oGfoiC4Ix1r6ppmaHOA6txqDGDELthRhn0GidkHsRVHH8Tsg8BMZB8y78WxxKRG6P-wfgufAS-PABm1HEzICtj4F9cyTAhuMu7tAQdZkJ8Wgojazm71NoBOovf2v628-SeDHqzLbgzfYQ9x66fgstqCiJg54tO8NPPOEIoxa9my_gUa-MAL</recordid><startdate>20121001</startdate><enddate>20121001</enddate><creator>Rosen, Philip</creator><creator>Pfister, David</creator><creator>Young, Denise</creator><creator>Petrovics, Gyorgy</creator><creator>Chen, Yongmei</creator><creator>Cullen, Jennifer</creator><creator>Böhm, Diana</creator><creator>Perner, Sven</creator><creator>Dobi, Albert</creator><creator>McLeod, David G</creator><creator>Sesterhenn, Isabell A</creator><creator>Srivastava, Shiv</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>20121001</creationdate><title>Differences in Frequency of ERG Oncoprotein Expression Between Index Tumors of Caucasian and African American Patients With Prostate Cancer</title><author>Rosen, Philip ; Pfister, David ; Young, Denise ; Petrovics, Gyorgy ; Chen, Yongmei ; Cullen, Jennifer ; Böhm, Diana ; Perner, Sven ; Dobi, Albert ; McLeod, David G ; Sesterhenn, Isabell A ; Srivastava, Shiv</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c497t-b873bfeb593d58268f2a83f8dabc04e67c9bab71cba36fa7bc719126b28587e93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>African Americans - genetics</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Carcinoma - genetics</topic><topic>Carcinoma - metabolism</topic><topic>Carcinoma - pathology</topic><topic>European Continental Ancestry Group - genetics</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Male</topic><topic>Male genital diseases</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Prostatic Neoplasms - metabolism</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Trans-Activators - genetics</topic><topic>Trans-Activators - metabolism</topic><topic>Transcriptional Regulator ERG</topic><topic>Tumors</topic><topic>Tumors of the urinary system</topic><topic>Urinary tract. Prostate gland</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rosen, Philip</creatorcontrib><creatorcontrib>Pfister, David</creatorcontrib><creatorcontrib>Young, Denise</creatorcontrib><creatorcontrib>Petrovics, Gyorgy</creatorcontrib><creatorcontrib>Chen, Yongmei</creatorcontrib><creatorcontrib>Cullen, Jennifer</creatorcontrib><creatorcontrib>Böhm, Diana</creatorcontrib><creatorcontrib>Perner, Sven</creatorcontrib><creatorcontrib>Dobi, Albert</creatorcontrib><creatorcontrib>McLeod, David G</creatorcontrib><creatorcontrib>Sesterhenn, Isabell A</creatorcontrib><creatorcontrib>Srivastava, Shiv</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Urology (Ridgewood, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rosen, Philip</au><au>Pfister, David</au><au>Young, Denise</au><au>Petrovics, Gyorgy</au><au>Chen, Yongmei</au><au>Cullen, Jennifer</au><au>Böhm, Diana</au><au>Perner, Sven</au><au>Dobi, Albert</au><au>McLeod, David G</au><au>Sesterhenn, Isabell A</au><au>Srivastava, Shiv</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differences in Frequency of ERG Oncoprotein Expression Between Index Tumors of Caucasian and African American Patients With Prostate Cancer</atitle><jtitle>Urology (Ridgewood, N.J.)</jtitle><addtitle>Urology</addtitle><date>2012-10-01</date><risdate>2012</risdate><volume>80</volume><issue>4</issue><spage>749</spage><epage>753</epage><pages>749-753</pages><issn>0090-4295</issn><eissn>1527-9995</eissn><coden>URGYAZ</coden><abstract>Objective To systematically evaluate the ETS-related gene (ERG) alterations in the multifocal tumor context using whole-mount prostatectomy specimens from African and Caucasian American patients matched for age, pathologic grade and stage. Oncogenic activation of the ERG is the most common early genomic alteration in patients with prostate cancer (CaP) in Western countries. However, ERG alterations have not been systematically examined in African American patients with a known greater risk of CaP incidence and mortality. Methods ERG oncoprotein expression was analyzed in 91 Caucasian and 91 African American patients with CaP, who were matched for age, Gleason score, and pathologic stage. A unique aspect of the present study was the evaluation of ERG in whole-mount prostatectomy sections, minimizing sampling bias and allowing the careful assessment of the ERG in the multifocal tumor context of CaP. Results The frequency of ERG-positive prostate tumors was significantly greater among Caucasian Americans than among African Americans when assessed in all tumor foci (41.9% vs 23.9%, P < .0001). A markedly greater frequency of ERG oncoprotein expression was noted between the index tumors of the Caucasian Americans (63.3%) and those of the African Americans (28.6%). Also, in the African American patients, the higher grade index tumors were predominantly ERG negative. Conclusion ERG typing of CaP established a major difference between the index tumors of Caucasian and African American patients. ERG-negative index tumors might indicate a less favorable outcome for African American patients. The results of the present study underscore that typing of CaP for the ERG could enhance our understanding of the biologic differences between the examined ethnic groups.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>22950997</pmid><doi>10.1016/j.urology.2012.07.001</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | African Americans - genetics Aged Biological and medical sciences Carcinoma - genetics Carcinoma - metabolism Carcinoma - pathology European Continental Ancestry Group - genetics Gynecology. Andrology. Obstetrics Humans Kaplan-Meier Estimate Male Male genital diseases Medical sciences Middle Aged Nephrology. Urinary tract diseases Prostatic Neoplasms - genetics Prostatic Neoplasms - metabolism Prostatic Neoplasms - pathology Trans-Activators - genetics Trans-Activators - metabolism Transcriptional Regulator ERG Tumors Tumors of the urinary system Urinary tract. Prostate gland Urology |
title | Differences in Frequency of ERG Oncoprotein Expression Between Index Tumors of Caucasian and African American Patients With Prostate Cancer |
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