The current state of preclinical prostate cancer animal models

被引:104
作者
Pienta, Kenneth J. [1 ,2 ]
Abate-Shen, Cory [3 ]
Agus, David B. [4 ]
Attar, Ricardo M. [5 ]
Chung, Leland W. K. [6 ]
Greenberg, Norman M. [7 ]
Hahn, William C. [8 ]
Isaacs, John T. [9 ,10 ]
Navone, Nora M. [11 ]
Peehl, Donna M. [12 ]
Simons, Jonathon W. [13 ]
Solit, David B. [14 ]
Soule, Howard R. [13 ]
VanDyke, Terry A. [15 ]
Weber, Michael J. [16 ,17 ]
Wu, Lily [18 ]
Vessella, Robert L. [19 ,20 ]
机构
[1] Univ Michigan, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Urol, Ann Arbor, MI 48109 USA
[3] Columbia Univ, Herbert Irving Canc Ctr, New York, NY USA
[4] Louis Warschaw Prostate Canc Ctr, Los Angeles, CA USA
[5] Bristol Myers Squibb Co, Princeton, NJ 08540 USA
[6] Emory Univ, Dept Urol, Atlanta, GA 30322 USA
[7] Fred Hutchinson Canc Res Ctr, Seattle, WA USA
[8] Harvard Univ, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[9] Johns Hopkins Med Sch, Dept Urol, Baltimore, MD USA
[10] Johns Hopkins Med Sch, Dept Oncol, Baltimore, MD USA
[11] Univ Texas MD Anderson Canc Ctr, Dept Genitourinary Oncol, Houston, TX 77030 USA
[12] Stanford Univ, Dept Urol, Stanford, CA 94305 USA
[13] Prostate Canc Fdn, Santa Monica, CA USA
[14] Mem Sloan Kettering Canc Ctr, Dept Genitourinary Oncol, New York, NY 10021 USA
[15] Univ N Carolina, Dept Genet, Chapel Hill, NC USA
[16] Univ Virginia, Ctr Canc, Charlottesville, VA 22908 USA
[17] Univ Virginia, Dept Microbiol, Charlottesville, VA 22908 USA
[18] Univ Calif Los Angeles, Dept Urol, Los Angeles, CA USA
[19] Univ Washington, Sch Med, Dept Urol, Seattle, WA 98195 USA
[20] Univ Washington, Sch Med, Dept Microbiol, Seattle, WA 98195 USA
关键词
mouse; genetically engineered; cell lines;
D O I
10.1002/pros.20726
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Prostate 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.
引用
收藏
页码:629 / 639
页数:11
相关论文
共 44 条
[1]  
Abdulkadir Sarki A, 2005, Future Oncol, V1, P351, DOI 10.1517/14796694.1.3.351
[2]  
ALCAIDE C, 2006, CLIN TRANSL ONCOL, V8, P148
[3]   Prolonged exposure to reduced levels of androgen accelerates prostate cancer progression in Nkx3.1; Pten mutant mice [J].
Banach-Petrosky, Whitney ;
Jessen, Walter J. ;
Ouyang, Xuesong ;
Gao, Hui ;
Rao, Jayashree ;
Quinn, John ;
Aronow, Bruce J. ;
Abate-Shen, Cory .
CANCER RESEARCH, 2007, 67 (19) :9089-9096
[4]  
Berezovska OP, 2006, CELL CYCLE, V5, P1886
[5]   Mouse Modeling in oncologic preclinical and translational research [J].
Carver, Brett S. ;
Pandolfi, Pier P. .
CLINICAL CANCER RESEARCH, 2006, 12 (18) :5305-5311
[6]   TMPRSS2-ERG gene fusion causing ERG overexpression precedes chromosome copy number changes in prostate carcinomas and paired HGPIN lesions [J].
Cerveira, Nuno ;
Ribeiro, Franclim R. ;
Peixoto, Ana ;
Costa, Vera ;
Henrique, Rui ;
Jeronimo, Carmen ;
Teixeira, Manuel R. .
NEOPLASIA, 2006, 8 (10) :826-832
[7]   Crucial role of p53-dependent cellular senescence in suppression of Pten-deficient tumorigenesis [J].
Chen, ZB ;
Trotman, LC ;
Shaffer, D ;
Lin, HK ;
Dotan, ZA ;
Niki, M ;
Koutcher, JA ;
Scher, HI ;
Ludwig, T ;
Gerald, W ;
Cordon-Cardo, C ;
Pandolfi, PP .
NATURE, 2005, 436 (7051) :725-730
[8]   ONCOGENE EXPRESSION IN PROSTATE-CANCER - DUNNING R3327 RAT DORSAL PROSTATIC ADENOCARCINOMA SYSTEM [J].
COOKE, DB ;
QUARMBY, VE ;
MICKEY, DD ;
ISAACS, JT ;
FRENCH, FS .
PROSTATE, 1988, 13 (04) :263-272
[9]   Mechanisms of androgen-refractory prostate cancer. [J].
Debes, JD ;
Tindall, DJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (15) :1488-1490
[10]   Combinatorial activities of Akt and B-Raf/Erk signaling in a mouse model of androgen-independent prostate cancer [J].
Gao, Hui ;
Ouyang, Xuesong ;
Banach-Petrosky, Whitney A. ;
Gerald, William L. ;
Shen, Michael M. ;
Abate-Shen, Cory .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (39) :14477-14482