Recent developments in prostate cancer biomarker research: therapeutic implications

被引:19
作者
Detchokul, Sujitra [1 ]
Frauman, Albert G. [1 ]
机构
[1] Univ Melbourne, Dept Med Austin Hlth No Hlth, Clin Pharmacol & Therapeut Unit, Heidelberg, Vic 3084, Australia
关键词
biomarker; prostate cancer; review; PHASE-I TRIAL; GROWTH-FACTOR-RECEPTOR; HISTONE DEACETYLASE INHIBITOR; SUBEROYLANILIDE HYDROXAMIC ACID; P53 PROTEIN ACCUMULATION; MEMBRANE ANTIGEN; CELLULAR IMMUNOTHERAPY; IMATINIB MESYLATE; MAMMALIAN TARGET; CLINICAL-TRIAL;
D O I
10.1111/j.1365-2125.2010.03766.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This review aims to present an overview of recent clinical trials targeting biomarkers in advanced prostate cancer. We searched ClinicalTrials.gov for early phase clinical trials on treatments of prostate cancer that have been recently completed, are ongoing or are actively recruiting participants. Drug targets and their mechanism of actions were assessed and summarized. Trials were categorized according to prostate cancer biomarkers that have potential as therapeutic targets. A total of 19 new therapeutic agents for the treatment of prostate cancer are included in this review. Trials are summarized according to the targeted biomarkers and are categorized into five therapeutic approaches: prostate cancer vaccine, epigenetic therapy, pro-apoptotic agents, prostate cancer antibodies and anti-angiogenesis approach. Some of the therapeutic agents reviewed showed promising results, warranting further investigation in late phase clinical trials. Recent novel prostate cancer biomarkers that made it through clinical trials and their relevance as drug targets are summarized. This review emphasizes the importance of specific prostate cancer biomarkers and their potentials as targets of the disease. Some clinical trials of targeted treatments in prostate cancer show promising results. Better understanding of disease mechanisms should potentially lead to more specific treatments for individual patients.
引用
收藏
页码:157 / 174
页数:18
相关论文
共 167 条
[1]   Molecular genetics of prostate cancer [J].
Abate-Shen, C ;
Shen, MM .
GENES & DEVELOPMENT, 2000, 14 (19) :2410-2434
[2]   Pilot study of rapamycin in patients with hormone-refractory prostate cancer [J].
Amato, Robert J. ;
Jac, Jaroslaw ;
Mohammad, Taqi ;
Saxena, Somya .
CLINICAL GENITOURINARY CANCER, 2008, 6 (02) :97-102
[3]   A novel anti-apoptosis gene, survivin, expressed in cancer and lymphoma [J].
Ambrosini, G ;
Adida, C ;
Altieri, DC .
NATURE MEDICINE, 1997, 3 (08) :917-921
[4]   Gene profiling study of G3139- and Bcl-2-targeting siRNAs identifies a unique G3139 molecular signature [J].
Anderson, EM ;
Miller, P ;
Ilsley, D ;
Marshall, W ;
Khvorova, A ;
Stein, CA ;
Benimetskaya, L .
CANCER GENE THERAPY, 2006, 13 (04) :406-414
[5]   Mortality Results from a Randomized Prostate-Cancer Screening Trial [J].
Andriole, Gerald L. ;
Grubb, Robert L., III ;
Buys, Saundra S. ;
Chia, David ;
Church, Timothy R. ;
Fouad, Mona N. ;
Gelmann, Edward P. ;
Kvale, Paul A. ;
Reding, Douglas J. ;
Weissfeld, Joel L. ;
Yokochi, Lance A. ;
Crawford, E. David ;
O'Brien, Barbara ;
Clapp, Jonathan D. ;
Rathmell, Joshua M. ;
Riley, Thomas L. ;
Hayes, Richard B. ;
Kramer, Barnett S. ;
Izmirlian, Grant ;
Miller, Anthony B. ;
Pinsky, Paul F. ;
Prorok, Philip C. ;
Gohagan, John K. ;
Berg, Christine D. .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 360 (13) :1310-1319
[6]   Phase-I clinical trial of IL-12 plasmid/lipopolymer complexes for the treatment of recurrent ovarian cancer [J].
Anwer, K. ;
Barnes, M. N. ;
Fewell, J. ;
Lewis, D. H. ;
Alvarez, R. D. .
GENE THERAPY, 2010, 17 (03) :360-369
[7]   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
[8]   Current Perspectives in Prostate Cancer Vaccines [J].
Arlen, Philip M. ;
Gulley, James L. .
ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2009, 9 (10) :1052-1057
[9]   A randomized phase II study of concurrent docetaxel plus vaccine versus vaccine alone in metastatic androgen-independent prostate cancer [J].
Arlen, PM ;
Gulley, JL ;
Parker, C ;
Skarupa, L ;
Pazdur, M ;
Panicali, D ;
Beetham, P ;
Tsang, KY ;
Grosenbach, DW ;
Feldman, J ;
Steinberg, SM ;
Jones, E ;
Chen, C ;
Marte, J ;
Schlom, J ;
Dahut, W .
CLINICAL CANCER RESEARCH, 2006, 12 (04) :1260-1269
[10]   Antiandrogen, vaccine and combination therapy in patients with nonmetastatic hormone refractory prostate cancer [J].
Arlen, PM ;
Gulley, JL ;
Todd, N ;
Lieberman, R ;
Steinberg, SM ;
Morin, S ;
Bastian, A ;
Marte, J ;
Tsang, KY ;
Beetham, P ;
Grosenbach, DW ;
Schlom, J ;
Dahut, W .
JOURNAL OF UROLOGY, 2005, 174 (02) :539-546