p300 in prostate cancer proliferation and progression
Although prostate cancer (PCa) is the most frequently diagnosed cancer in males, little is known about the mechanisms involved in its progression. Recent in vitro studies suggest that coactivators of the androgen receptor play an important role in PCa progression. We have shown previously that p300...
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Veröffentlicht in: | Cancer research (Chicago, Ill.) Ill.), 2003-11, Vol.63 (22), p.7638-7640 |
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creator | DEBES, Jose D SEBO, Thomas J LOHSE, Christine M MURPHY, Linda M HAUGEN, De Anna L TINDALL, Donald J |
description | Although prostate cancer (PCa) is the most frequently diagnosed cancer in males, little is known about the mechanisms involved in its progression. Recent in vitro studies suggest that coactivators of the androgen receptor play an important role in PCa progression. We have shown previously that p300 is involved in androgen receptor transactivation. In the present work, we studied 95 patients with biopsy-proven PCa who underwent prostatectomy as treatment of their tumors between 1995 and 1998. We found that p300 correlated with in vivo proliferation (P = 0.009) as determined by MIB-I expression. Moreover, high levels of p300 in biopsies predicted larger tumor volumes (P < 0.001), extraprostatic extension (P = 0.003), and seminal vesicle involvement (P = 0.002) at prostatectomy, as well as PCa progression after surgery (P = 0.01). Furthermore, we found that the disruption of p300 transcripts through small interfering RNA inhibited PCa cell proliferation both at the basal level and on interleukin 6 stimulation. We conclude that p300 plays an important role in PCa cell proliferation, as well as PCa progression. |
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Recent in vitro studies suggest that coactivators of the androgen receptor play an important role in PCa progression. We have shown previously that p300 is involved in androgen receptor transactivation. In the present work, we studied 95 patients with biopsy-proven PCa who underwent prostatectomy as treatment of their tumors between 1995 and 1998. We found that p300 correlated with in vivo proliferation (P = 0.009) as determined by MIB-I expression. Moreover, high levels of p300 in biopsies predicted larger tumor volumes (P < 0.001), extraprostatic extension (P = 0.003), and seminal vesicle involvement (P = 0.002) at prostatectomy, as well as PCa progression after surgery (P = 0.01). Furthermore, we found that the disruption of p300 transcripts through small interfering RNA inhibited PCa cell proliferation both at the basal level and on interleukin 6 stimulation. We conclude that p300 plays an important role in PCa cell proliferation, as well as PCa progression.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 14633682</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Acetyltransferases - biosynthesis ; Acetyltransferases - physiology ; Antineoplastic agents ; Biological and medical sciences ; Cell Cycle Proteins - biosynthesis ; Cell Cycle Proteins - physiology ; Cell Division - physiology ; Cell Line, Tumor ; Disease Progression ; Histone Acetyltransferases ; Humans ; Ki-67 Antigen - biosynthesis ; Male ; Medical sciences ; p300-CBP Transcription Factors ; Pharmacology. Drug treatments ; Ploidies ; Prostatectomy ; Prostatic Neoplasms - genetics ; Prostatic Neoplasms - metabolism ; Prostatic Neoplasms - pathology ; Prostatic Neoplasms - surgery ; Transcription Factors - physiology ; Tumors</subject><ispartof>Cancer research (Chicago, Ill.), 2003-11, Vol.63 (22), p.7638-7640</ispartof><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15324648$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14633682$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>DEBES, Jose D</creatorcontrib><creatorcontrib>SEBO, Thomas J</creatorcontrib><creatorcontrib>LOHSE, Christine M</creatorcontrib><creatorcontrib>MURPHY, Linda M</creatorcontrib><creatorcontrib>HAUGEN, De Anna L</creatorcontrib><creatorcontrib>TINDALL, Donald J</creatorcontrib><title>p300 in prostate cancer proliferation and progression</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>Although prostate cancer (PCa) is the most frequently diagnosed cancer in males, little is known about the mechanisms involved in its progression. Recent in vitro studies suggest that coactivators of the androgen receptor play an important role in PCa progression. We have shown previously that p300 is involved in androgen receptor transactivation. In the present work, we studied 95 patients with biopsy-proven PCa who underwent prostatectomy as treatment of their tumors between 1995 and 1998. We found that p300 correlated with in vivo proliferation (P = 0.009) as determined by MIB-I expression. Moreover, high levels of p300 in biopsies predicted larger tumor volumes (P < 0.001), extraprostatic extension (P = 0.003), and seminal vesicle involvement (P = 0.002) at prostatectomy, as well as PCa progression after surgery (P = 0.01). Furthermore, we found that the disruption of p300 transcripts through small interfering RNA inhibited PCa cell proliferation both at the basal level and on interleukin 6 stimulation. We conclude that p300 plays an important role in PCa cell proliferation, as well as PCa progression.</description><subject>Acetyltransferases - biosynthesis</subject><subject>Acetyltransferases - physiology</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Cell Cycle Proteins - biosynthesis</subject><subject>Cell Cycle Proteins - physiology</subject><subject>Cell Division - physiology</subject><subject>Cell Line, Tumor</subject><subject>Disease Progression</subject><subject>Histone Acetyltransferases</subject><subject>Humans</subject><subject>Ki-67 Antigen - biosynthesis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>p300-CBP Transcription Factors</subject><subject>Pharmacology. Drug treatments</subject><subject>Ploidies</subject><subject>Prostatectomy</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Prostatic Neoplasms - metabolism</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Prostatic Neoplasms - surgery</subject><subject>Transcription Factors - physiology</subject><subject>Tumors</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1LAzEQhoMotlb_guxFbwtJJpPMHqX4BQUvel6mm0RXttuabA_-eyNWPHoanuHhfeE9EnOFQLUzBo_FXEpJNRqnZ-Is5_eCqCSeipkyFsCSngvcgZRVP1a7tM0TT6HqeOxC-uahjyHx1G_Hikf__XlNIefC5-Ik8pDDxeEuxMvd7fPyoV493T8ub1b1G0g91UQGY9TBq4YsOfIYrV87Ctr5qBiURXAInWMdfcOIzqtARJE4sAUNC3H9k1u6P_YhT-2mz10YBh7Ddp9bp6DRytC_omo0GCBXxMuDuF9vgm93qd9w-mx_FynC1UHg3PEQU5mjz38egja2NH4BkwxpJA</recordid><startdate>20031115</startdate><enddate>20031115</enddate><creator>DEBES, Jose D</creator><creator>SEBO, Thomas J</creator><creator>LOHSE, Christine M</creator><creator>MURPHY, Linda M</creator><creator>HAUGEN, De Anna L</creator><creator>TINDALL, Donald J</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TO</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20031115</creationdate><title>p300 in prostate cancer proliferation and progression</title><author>DEBES, Jose D ; SEBO, Thomas J ; LOHSE, Christine M ; MURPHY, Linda M ; HAUGEN, De Anna L ; TINDALL, Donald J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h302t-8845ff2ed1986878d5f6db78e27df1a31653753c7a2fd9a557d1e888f8aea6323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Acetyltransferases - biosynthesis</topic><topic>Acetyltransferases - physiology</topic><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>Cell Cycle Proteins - biosynthesis</topic><topic>Cell Cycle Proteins - physiology</topic><topic>Cell Division - physiology</topic><topic>Cell Line, Tumor</topic><topic>Disease Progression</topic><topic>Histone Acetyltransferases</topic><topic>Humans</topic><topic>Ki-67 Antigen - biosynthesis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>p300-CBP Transcription Factors</topic><topic>Pharmacology. Drug treatments</topic><topic>Ploidies</topic><topic>Prostatectomy</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Prostatic Neoplasms - metabolism</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Prostatic Neoplasms - surgery</topic><topic>Transcription Factors - physiology</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DEBES, Jose D</creatorcontrib><creatorcontrib>SEBO, Thomas J</creatorcontrib><creatorcontrib>LOHSE, Christine M</creatorcontrib><creatorcontrib>MURPHY, Linda M</creatorcontrib><creatorcontrib>HAUGEN, De Anna L</creatorcontrib><creatorcontrib>TINDALL, Donald J</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>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DEBES, Jose D</au><au>SEBO, Thomas J</au><au>LOHSE, Christine M</au><au>MURPHY, Linda M</au><au>HAUGEN, De Anna L</au><au>TINDALL, Donald J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>p300 in prostate cancer proliferation and progression</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>2003-11-15</date><risdate>2003</risdate><volume>63</volume><issue>22</issue><spage>7638</spage><epage>7640</epage><pages>7638-7640</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>Although prostate cancer (PCa) is the most frequently diagnosed cancer in males, little is known about the mechanisms involved in its progression. Recent in vitro studies suggest that coactivators of the androgen receptor play an important role in PCa progression. We have shown previously that p300 is involved in androgen receptor transactivation. In the present work, we studied 95 patients with biopsy-proven PCa who underwent prostatectomy as treatment of their tumors between 1995 and 1998. We found that p300 correlated with in vivo proliferation (P = 0.009) as determined by MIB-I expression. Moreover, high levels of p300 in biopsies predicted larger tumor volumes (P < 0.001), extraprostatic extension (P = 0.003), and seminal vesicle involvement (P = 0.002) at prostatectomy, as well as PCa progression after surgery (P = 0.01). Furthermore, we found that the disruption of p300 transcripts through small interfering RNA inhibited PCa cell proliferation both at the basal level and on interleukin 6 stimulation. We conclude that p300 plays an important role in PCa cell proliferation, as well as PCa progression.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>14633682</pmid><tpages>3</tpages></addata></record> |
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subjects | Acetyltransferases - biosynthesis Acetyltransferases - physiology Antineoplastic agents Biological and medical sciences Cell Cycle Proteins - biosynthesis Cell Cycle Proteins - physiology Cell Division - physiology Cell Line, Tumor Disease Progression Histone Acetyltransferases Humans Ki-67 Antigen - biosynthesis Male Medical sciences p300-CBP Transcription Factors Pharmacology. Drug treatments Ploidies Prostatectomy Prostatic Neoplasms - genetics Prostatic Neoplasms - metabolism Prostatic Neoplasms - pathology Prostatic Neoplasms - surgery Transcription Factors - physiology Tumors |
title | p300 in prostate cancer proliferation and progression |
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