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GREB1 is a novel androgen-regulated gene required for prostate cancer growth

dc.contributor.authorRae, James Michaelen_US
dc.contributor.authorJohnson, Michael D.en_US
dc.contributor.authorCordero, Kevin E.en_US
dc.contributor.authorScheys, Joshua O.en_US
dc.contributor.authorLarios, José M.en_US
dc.contributor.authorGottardis, Marco M.en_US
dc.contributor.authorPienta, Kenneth J.en_US
dc.contributor.authorLippman, Marc E.en_US
dc.date.accessioned2007-01-17T15:52:26Z
dc.date.available2007-01-17T15:52:26Z
dc.date.issued2006en_US
dc.identifier.citationRae, James M.; Johnson, Michael D.; Cordero, Kevin E.; Scheys, Joshua O.; Larios, JosÉ M.; Gottardis, Marco M.; Pienta, Kenneth J.; Lippman, Marc E. (2006)."GREB1 is a novel androgen-regulated gene required for prostate cancer growth." The Prostate 9999(9999): n/a-n/a. <http://hdl.handle.net/2027.42/49275>en_US
dc.identifier.issn0270-4137en_US
dc.identifier.issn1097-0045en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/49275
dc.description.abstractBACKGROUND Gene regulated in breast cancer 1 (GREB1) is a novel estrogen-regulated gene shown to play a pivotal role in hormone-stimulated breast cancer growth. GREB1 is expressed in the prostate and its putative promoter contains potential androgen receptor (AR) response elements. METHODS We investigated the effects of androgens on GREB1 expression and its role in androgen-dependent prostate cancer growth. RESULTS Real-time PCR demonstrated high level GREB1 expression in benign prostatic hypertrophy (BPH), localized prostate cancer (L-PCa), and hormone refractory prostate cancer (HR-PCa). Androgen treatment of AR-positive prostate cancer cells induced dose-dependent GREB1 expression, which was blocked by anti-androgens. AR binding to the GREB1 promoter was confirmed by chromatin immunoprecipitation (ChIP) assays. Suppression of GREB1 by RNA interference blocked androgen-stimulated LNCaP cell proliferation. CONCLUSIONS GREB1 is expressed in proliferating prostatic tissue and prostate cancer, is regulated by androgens, and suppression of GREB1 blocks androgen-induced growth suggesting GREB1 may be critically involved in prostate cancer proliferation. Prostate © 2006 Wiley-Liss, Inc.en_US
dc.format.extent262220 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCancer Research, Oncology and Pathologyen_US
dc.titleGREB1 is a novel androgen-regulated gene required for prostate cancer growthen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Hematology Oncology, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Michigan ; Division of Hematology and Oncology, Department of Internal Medicine, University of Michigan Medical Center, 5323 Med Sci 1, 1150 W. Medical Center Drive, Ann Arbor, MI 48109.en_US
dc.contributor.affiliationumDivision of Hematology Oncology, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDivision of Hematology Oncology, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDivision of Hematology Oncology, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDivision of Hematology Oncology, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDivision of Hematology Oncology, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherDepartment of Oncology, Georgetown University, Washington, District of Columbiaen_US
dc.contributor.affiliationotherDepartment of Discovery Biology, Bristol–Myers Squibb Pharmaceutical Research Institute, Princeton, New Jerseyen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/49275/1/20403_fta.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/pros.20403en_US
dc.identifier.sourceThe Prostateen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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