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The current state of preclinical prostate cancer animal models

dc.contributor.authorPienta, Kenneth J.en_US
dc.contributor.authorAbate-Shen, Coryen_US
dc.contributor.authorAgus, David B.en_US
dc.contributor.authorAttar, Ricardo M.en_US
dc.contributor.authorChung, Leland W. K.en_US
dc.contributor.authorGreenberg, Norman M.en_US
dc.contributor.authorHahn, William C.en_US
dc.contributor.authorIsaacs, John T.en_US
dc.contributor.authorNavone, Nora M.en_US
dc.contributor.authorPeehl, Donna M.en_US
dc.contributor.authorSimons, Jonathon W.en_US
dc.contributor.authorSolit, David B.en_US
dc.contributor.authorSoule, Howard R.en_US
dc.contributor.authorVanDyke, Terry A.en_US
dc.contributor.authorWeber, Michael J.en_US
dc.contributor.authorWu, Lilyen_US
dc.contributor.authorVessella, Robert L.en_US
dc.date.accessioned2008-03-31T18:38:51Z
dc.date.available2009-05-04T19:09:21Zen_US
dc.date.issued2008-05-01en_US
dc.identifier.citationPienta, Kenneth J.; Abate-Shen, Cory; Agus, David B.; Attar, Ricardo M.; Chung, Leland W.K.; Greenberg, Norman M.; Hahn, William C.; Isaacs, John T.; Navone, Nora M.; Peehl, Donna M.; Simons, Jonathon W.; Solit, David B.; Soule, Howard R.; VanDyke, Terry A.; Weber, Michael J.; Wu, Lily; Vessella, Robert L. (2008). "The current state of preclinical prostate cancer animal models." The Prostate 68(6): 629-639. <http://hdl.handle.net/2027.42/58068>en_US
dc.identifier.issn0270-4137en_US
dc.identifier.issn1097-0045en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/58068
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=18213636&dopt=citation
dc.description.abstractProstate cancer continues to be a major cause of morbidity and mortality in men around the world. The field of prostate cancer research continues to be hindered by the lack of relevant preclinical models to study tumorigenesis and to further development of effective prevention and therapeutic strategies. The Prostate Cancer Foundation held a Prostate Cancer Models Working Group (PCMWG) Summit on August 6th and 7th, 2007 to address these issues. The PCMWG reviewed the state of prostate cancer preclinical models and identified the current limitations of cell line, xenograft and genetically engineered mouse models that have hampered the transition of scientific findings from these models to human clinical trials. In addition the PCMWG identified administrative issues that inhibit the exchange of models and impede greater interactions between academic centers and these centers with industry. The PCMWG identified potential solutions for discovery bottlenecks that include: (1) insufficient number of models with insufficient molecular and biologic diversity to reflect human cancer, (2) a lack of understanding of the molecular events that define tumorigenesis, (3) a lack of tools for studying tumor–host interactions, (4) difficulty in accessing model systems across institutions, and (5) addressing why preclinical studies appear not to be predictive of human clinical trials. It should be possible to apply the knowledge gained molecular and epigenetic studies to develop new cell lines and models that mimic progressive and fatal prostate cancer and ultimately improve interventions. Prostate 68: 629–639, 2008. © 2008 Wiley-Liss, Inc.en_US
dc.format.extent366881 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
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.titleThe current state of preclinical prostate cancer animal modelsen_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.affiliationumUniversity of Michigan, Departments of Internal Medicine and Urology, Ann Arbor, MI ; 1500 E. Medical Center Drive, 7308 CCC, Ann Arbor, MI 48109.en_US
dc.contributor.affiliationotherColumbia University, Herbert Irving Cancer Center, New York, NYen_US
dc.contributor.affiliationotherCedars-Sinai, Louis Warschaw Prostate Cancer Center, Los Angeles, CAen_US
dc.contributor.affiliationotherBristol-Myers Squibb, New Jerseyen_US
dc.contributor.affiliationotherEmory University, Department of Urology, Atlanta, GAen_US
dc.contributor.affiliationotherFred Hutchinson Cancer Center, Seattle, WAen_US
dc.contributor.affiliationotherHarvard University, Dana-Farber Cancer Institute, Department of Medical Oncology, Boston, MAen_US
dc.contributor.affiliationotherJohns Hopkins Medical School, Departments of Urology and Oncology, Baltimore, MDen_US
dc.contributor.affiliationotherUniversity of Texas, M.D. Anderson Cancer Center, Department of Genitourinary Oncology, Houston, TXen_US
dc.contributor.affiliationotherStanford University, Department of Urology, Stanford, CAen_US
dc.contributor.affiliationotherProstate Cancer Foundation, Santa Monica, CAen_US
dc.contributor.affiliationotherMemorial Sloan-Kettering Cancer Center, Department of Genitourinary Oncology, New York, NYen_US
dc.contributor.affiliationotherProstate Cancer Foundation, Santa Monica, CAen_US
dc.contributor.affiliationotherUniversity of North Carolina, Department of Genetics, Chapel Hill, NCen_US
dc.contributor.affiliationotherUniversity of Virginia, Cancer Center and Department of Microbiology, Charlottesville, VAen_US
dc.contributor.affiliationotherUniversity of California-Los Angeles, Department of Urology, Los Angeles, CAen_US
dc.contributor.affiliationotherUniversity of Washington School of Medicine, Departments of Urology and Microbiology, Seattle, WAen_US
dc.identifier.pmid18213636
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/58068/1/20726_ftp.pdf
dc.identifier.doihttp://dx.doi.org/10.1002/pros.20726en_US
dc.identifier.sourceThe Prostateen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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