Nuclear MTA1 overexpression is associated with aggressive prostate cancer, recurrence and metastasis in African Americans
Metastasis-associated protein 1 (MTA1), a negative epigenetic modifier, plays a critical role in prostate cancer (PCa) progression. We hypothesized that MTA1 overexpression in primary tumor tissues can predict PCa aggressiveness and metastasis. Immunohistochemical staining of MTA1 was done on archiv...
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description | Metastasis-associated protein 1 (MTA1), a negative epigenetic modifier, plays a critical role in prostate cancer (PCa) progression. We hypothesized that MTA1 overexpression in primary tumor tissues can predict PCa aggressiveness and metastasis. Immunohistochemical staining of MTA1 was done on archival PCa specimens from University of Mississippi Medical Center and University of Iowa. We found that nuclear MTA1 overexpression was positively correlated with the severity of disease progression reaching its highest levels in metastatic PCa. Nuclear MTA1 overexpression was significantly associated with Gleason > 7 tumors in African Americans but not in Caucasians. It was also a predictor of recurrent disease. We concluded that MTA1 nuclear overexpression may be a prognostic indicator and a future therapeutic target for aggressive PCa in African American men. Our findings may be useful for categorizing African American patients with a higher probability of recurrent disease and metastasis from those who are likely to remain metastasis-free. |
doi_str_mv | 10.1038/srep02331 |
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We hypothesized that MTA1 overexpression in primary tumor tissues can predict PCa aggressiveness and metastasis. Immunohistochemical staining of MTA1 was done on archival PCa specimens from University of Mississippi Medical Center and University of Iowa. We found that nuclear MTA1 overexpression was positively correlated with the severity of disease progression reaching its highest levels in metastatic PCa. Nuclear MTA1 overexpression was significantly associated with Gleason > 7 tumors in African Americans but not in Caucasians. It was also a predictor of recurrent disease. We concluded that MTA1 nuclear overexpression may be a prognostic indicator and a future therapeutic target for aggressive PCa in African American men. Our findings may be useful for categorizing African American patients with a higher probability of recurrent disease and metastasis from those who are likely to remain metastasis-free.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep02331</identifier><identifier>PMID: 23900262</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/67 ; 631/67/1857 ; 692/308/1892 ; 692/699 ; African Americans ; Biomarkers, Tumor - metabolism ; Black or African American - statistics & numerical data ; Cell Nucleus - metabolism ; Histone Deacetylases - metabolism ; Humanities and Social Sciences ; Humans ; Iowa - epidemiology ; Male ; Metastases ; Metastasis ; Middle Aged ; Mississippi - epidemiology ; multidisciplinary ; Neoplasm Recurrence, Local - ethnology ; Neoplasm Recurrence, Local - metabolism ; Prevalence ; Prostate cancer ; Prostatic Neoplasms - ethnology ; Prostatic Neoplasms - metabolism ; Prostatic Neoplasms - secondary ; Recurrence ; Repressor Proteins - metabolism ; Risk Assessment ; Science ; Trans-Activators ; Tumors ; Up-Regulation</subject><ispartof>Scientific reports, 2013-07, Vol.3 (1), p.2331-2331, Article 2331</ispartof><rights>The Author(s) 2013</rights><rights>Copyright Nature Publishing Group Jul 2013</rights><rights>Copyright © 2013, Macmillan Publishers Limited. All rights reserved 2013 Macmillan Publishers Limited. All rights reserved</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-f9b968be9b6f73d26953ea953c26b47b5d429d96acd488ebdacb7b19c384299b3</citedby><cites>FETCH-LOGICAL-c438t-f9b968be9b6f73d26953ea953c26b47b5d429d96acd488ebdacb7b19c384299b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728596/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728596/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27922,27923,41118,42187,51574,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23900262$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dias, Steven J.</creatorcontrib><creatorcontrib>Zhou, Xinchun</creatorcontrib><creatorcontrib>Ivanovic, Marina</creatorcontrib><creatorcontrib>Gailey, Michael P.</creatorcontrib><creatorcontrib>Dhar, Swati</creatorcontrib><creatorcontrib>Zhang, Liangfen</creatorcontrib><creatorcontrib>He, Zhi</creatorcontrib><creatorcontrib>Penman, Alan D.</creatorcontrib><creatorcontrib>Vijayakumar, Srinivasan</creatorcontrib><creatorcontrib>Levenson, Anait S.</creatorcontrib><title>Nuclear MTA1 overexpression is associated with aggressive prostate cancer, recurrence and metastasis in African Americans</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Metastasis-associated protein 1 (MTA1), a negative epigenetic modifier, plays a critical role in prostate cancer (PCa) progression. We hypothesized that MTA1 overexpression in primary tumor tissues can predict PCa aggressiveness and metastasis. Immunohistochemical staining of MTA1 was done on archival PCa specimens from University of Mississippi Medical Center and University of Iowa. We found that nuclear MTA1 overexpression was positively correlated with the severity of disease progression reaching its highest levels in metastatic PCa. Nuclear MTA1 overexpression was significantly associated with Gleason > 7 tumors in African Americans but not in Caucasians. It was also a predictor of recurrent disease. We concluded that MTA1 nuclear overexpression may be a prognostic indicator and a future therapeutic target for aggressive PCa in African American men. Our findings may be useful for categorizing African American patients with a higher probability of recurrent disease and metastasis from those who are likely to remain metastasis-free.</description><subject>631/67</subject><subject>631/67/1857</subject><subject>692/308/1892</subject><subject>692/699</subject><subject>African Americans</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Black or African American - statistics & numerical data</subject><subject>Cell Nucleus - metabolism</subject><subject>Histone Deacetylases - metabolism</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Iowa - epidemiology</subject><subject>Male</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Mississippi - epidemiology</subject><subject>multidisciplinary</subject><subject>Neoplasm Recurrence, Local - ethnology</subject><subject>Neoplasm Recurrence, Local - metabolism</subject><subject>Prevalence</subject><subject>Prostate cancer</subject><subject>Prostatic Neoplasms - ethnology</subject><subject>Prostatic Neoplasms - metabolism</subject><subject>Prostatic Neoplasms - secondary</subject><subject>Recurrence</subject><subject>Repressor Proteins - metabolism</subject><subject>Risk Assessment</subject><subject>Science</subject><subject>Trans-Activators</subject><subject>Tumors</subject><subject>Up-Regulation</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNplkV1vFCEUhonR2Kb2wj9gSLzRxlW-hoGbJpumfiRVb-o1AebMlmYGRphZ7b8Xu3WzKhdwyPvkPQdehJ5T8pYSrt6VDBNhnNNH6JgR0awYZ-zxQX2ETku5JXU1TAuqn6IjxjUhTLJjdPdl8QPYjD9frylOW8jwc8pQSkgRh4JtKckHO0OHf4T5BtvN5l7dAp5yKnNVsLfRQ36DM_glZ6gXbGOHR5htBUp1CRGv-xwqiNcj3BflGXrS26HA6cN5gr69v7y--Li6-vrh08X6auUFV_Oq105L5UA72be8Y1I3HGzdPJNOtK7pBNOdltZ3QilwnfWudVR7rqqgHT9B5zvfaXEjdB7inO1gphxGm-9MssH8rcRwYzZpa3jLVKNlNXj1YJDT9wXKbMZQPAyDjZCWYqigUmqhGanoy3_Q27TkWJ9nqNKt4EIxVqnXO8rXH6zx9fthKDG_MzX7TCv74nD6PfknwQqc7YBSpbiBfNDyP7dfpkytmg</recordid><startdate>20130731</startdate><enddate>20130731</enddate><creator>Dias, Steven J.</creator><creator>Zhou, Xinchun</creator><creator>Ivanovic, Marina</creator><creator>Gailey, Michael P.</creator><creator>Dhar, Swati</creator><creator>Zhang, Liangfen</creator><creator>He, Zhi</creator><creator>Penman, Alan D.</creator><creator>Vijayakumar, Srinivasan</creator><creator>Levenson, Anait S.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</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>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20130731</creationdate><title>Nuclear MTA1 overexpression is associated with aggressive prostate cancer, recurrence and metastasis in African Americans</title><author>Dias, Steven J. ; Zhou, Xinchun ; Ivanovic, Marina ; Gailey, Michael P. ; Dhar, Swati ; Zhang, Liangfen ; He, Zhi ; Penman, Alan D. ; Vijayakumar, Srinivasan ; Levenson, Anait S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-f9b968be9b6f73d26953ea953c26b47b5d429d96acd488ebdacb7b19c384299b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>631/67</topic><topic>631/67/1857</topic><topic>692/308/1892</topic><topic>692/699</topic><topic>African Americans</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Black or African American - statistics & numerical data</topic><topic>Cell Nucleus - metabolism</topic><topic>Histone Deacetylases - metabolism</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Iowa - epidemiology</topic><topic>Male</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Mississippi - epidemiology</topic><topic>multidisciplinary</topic><topic>Neoplasm Recurrence, Local - ethnology</topic><topic>Neoplasm Recurrence, Local - metabolism</topic><topic>Prevalence</topic><topic>Prostate cancer</topic><topic>Prostatic Neoplasms - ethnology</topic><topic>Prostatic Neoplasms - metabolism</topic><topic>Prostatic Neoplasms - secondary</topic><topic>Recurrence</topic><topic>Repressor Proteins - metabolism</topic><topic>Risk Assessment</topic><topic>Science</topic><topic>Trans-Activators</topic><topic>Tumors</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dias, Steven J.</creatorcontrib><creatorcontrib>Zhou, Xinchun</creatorcontrib><creatorcontrib>Ivanovic, Marina</creatorcontrib><creatorcontrib>Gailey, Michael P.</creatorcontrib><creatorcontrib>Dhar, Swati</creatorcontrib><creatorcontrib>Zhang, Liangfen</creatorcontrib><creatorcontrib>He, Zhi</creatorcontrib><creatorcontrib>Penman, Alan D.</creatorcontrib><creatorcontrib>Vijayakumar, Srinivasan</creatorcontrib><creatorcontrib>Levenson, Anait S.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</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 One Sustainability</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>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>Publicly Available Content Database</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dias, Steven J.</au><au>Zhou, Xinchun</au><au>Ivanovic, Marina</au><au>Gailey, Michael P.</au><au>Dhar, Swati</au><au>Zhang, Liangfen</au><au>He, Zhi</au><au>Penman, Alan D.</au><au>Vijayakumar, Srinivasan</au><au>Levenson, Anait S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nuclear MTA1 overexpression is associated with aggressive prostate cancer, recurrence and metastasis in African Americans</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2013-07-31</date><risdate>2013</risdate><volume>3</volume><issue>1</issue><spage>2331</spage><epage>2331</epage><pages>2331-2331</pages><artnum>2331</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Metastasis-associated protein 1 (MTA1), a negative epigenetic modifier, plays a critical role in prostate cancer (PCa) progression. We hypothesized that MTA1 overexpression in primary tumor tissues can predict PCa aggressiveness and metastasis. Immunohistochemical staining of MTA1 was done on archival PCa specimens from University of Mississippi Medical Center and University of Iowa. We found that nuclear MTA1 overexpression was positively correlated with the severity of disease progression reaching its highest levels in metastatic PCa. Nuclear MTA1 overexpression was significantly associated with Gleason > 7 tumors in African Americans but not in Caucasians. It was also a predictor of recurrent disease. We concluded that MTA1 nuclear overexpression may be a prognostic indicator and a future therapeutic target for aggressive PCa in African American men. Our findings may be useful for categorizing African American patients with a higher probability of recurrent disease and metastasis from those who are likely to remain metastasis-free.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>23900262</pmid><doi>10.1038/srep02331</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/67 631/67/1857 692/308/1892 692/699 African Americans Biomarkers, Tumor - metabolism Black or African American - statistics & numerical data Cell Nucleus - metabolism Histone Deacetylases - metabolism Humanities and Social Sciences Humans Iowa - epidemiology Male Metastases Metastasis Middle Aged Mississippi - epidemiology multidisciplinary Neoplasm Recurrence, Local - ethnology Neoplasm Recurrence, Local - metabolism Prevalence Prostate cancer Prostatic Neoplasms - ethnology Prostatic Neoplasms - metabolism Prostatic Neoplasms - secondary Recurrence Repressor Proteins - metabolism Risk Assessment Science Trans-Activators Tumors Up-Regulation |
title | Nuclear MTA1 overexpression is associated with aggressive prostate cancer, recurrence and metastasis in African Americans |
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