Molecular markers of prostate cancer outcome

被引:154
作者
Quinn, DI
Henshall, SM
Sutherland, RL
机构
[1] Univ So Calif, Kenneth Norris Jr Comprehens Canc Ctr, Keck Sch Med, Div Oncol, Los Angeles, CA 90033 USA
[2] Georgetown Univ, Lombardi Comprehens Canc Ctr, Div Oncol, Washington, DC 20007 USA
[3] St Vincents Hosp, Canc Res Program, Garvan Inst Med Res, Sydney, NSW 2010, Australia
基金
美国国家卫生研究院;
关键词
prostate cancer; prognosis; molecular markers; oncogenes; tumor suppressor genes;
D O I
10.1016/j.ejca.2004.12.035
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Molecular markers have the potential to serve not only as prognostic factors but may be targets for new therapeutic strategies and predictors of response in a range of cancers. Prostate cancer development and progression is predicated on a series of genetic and epigenetic events within the prostate cell and its milieu. Within this review, we identify candidate molecules involved in diverse processes such as cell proliferation, death and apoptosis, signal transduction, androgen receptor (AR) signalling, cellular adhesion and angiogenesis that are linked to outcome in prostate cancer. Current markers with potential prognostic value include p53, Bcl-2, p16(INK4A), p27(Kip1), c-Myc, AR, E-cadherin and vascular endothelial growth factor. Evolving technology permits the identification of an increasing number of molecular markers with prognosis and predictive potential. We also review the use of gene microarray analysis in gene discovery as a means of identifying and cosegregating novel markers of prostate cancer outcome. By integrating selected markers into prospective clinical trials, there is potential for us to provide specific targeted therapy tailored for an increasing number of patients. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:858 / 887
页数:30
相关论文
共 440 条
[1]   α-Catenin expression has prognostic value in local and locally advanced prostate cancer [J].
Aaltomaa, S ;
Lipponen, P ;
Ala-Opas, M ;
Eskelinen, M ;
Kosma, VM .
BRITISH JOURNAL OF CANCER, 1999, 80 (3-4) :477-482
[2]  
Aaltomaa S, 1999, PROSTATE, V38, P175
[3]  
Aaltomaa S, 1999, PROSTATE, V39, P8
[4]   The p53 network [J].
Agarwal, ML ;
Taylor, WR ;
Chernov, MV ;
Chernova, OB ;
Stark, GR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (01) :1-4
[5]   Prostate cancer cell cycle regulators: Response to androgen withdrawal and development of androgen independence [J].
Agus, DB ;
Cordon-Cardo, C ;
Fox, W ;
Drobnjak, M ;
Koff, A ;
Golde, DW ;
Scher, HI .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (21) :1869-1876
[6]  
AIHARA M, 1995, CANCER-AM CANCER SOC, V75, P522, DOI 10.1002/1097-0142(19950115)75:2<522::AID-CNCR2820750215>3.0.CO
[7]  
2-W
[8]   INTERPHASE CYTOGENETICS OF PROSTATIC ADENOCARCINOMA AND PRECURSOR LESIONS - ANALYSIS OF 25 RADICAL PROSTATECTOMIES AND 17 ADJACENT PROSTATIC INTRAEPITHELIAL NEOPLASIAS [J].
ALERS, JC ;
KRIJTENBURG, PJ ;
VISSERS, KJ ;
BOSMAN, FT ;
VANDERKWAST, TH ;
VANDEKKEN, H .
GENES CHROMOSOMES & CANCER, 1995, 12 (04) :241-250
[9]   MYC-MAX-MAD - A TRANSCRIPTION FACTOR NETWORK CONTROLLING CELL-CYCLE PROGRESSION, DIFFERENTIATION AND DEATH [J].
AMATI, B ;
LAND, H .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1994, 4 (01) :102-108
[10]   bcl-2 Overexpression combined with p53 protein accumulation correlates with hormone-refractory prostate cancer [J].
Apakama, I ;
Robinson, MC ;
Walter, NM ;
Charlton, RG ;
Royds, JA ;
Fuller, CE ;
Neal, DE ;
Hamdy, FC .
BRITISH JOURNAL OF CANCER, 1996, 74 (08) :1258-1262