Androgen Hypersensitivity in Prostate Cancer: Molecular Perspectives on Androgen Deprivation Therapy Strategies

被引:7
作者
Foley, Ruth
Marignol, Laure
Keane, John P. [2 ]
Lynch, Thomas H. [2 ]
Hollywood, Donal [1 ]
机构
[1] St James Hosp, Acad Unit Clin & Mol Oncol, Trinity Ctr Hlth Sci, Trinity Coll,Prostate Mol Oncol Grp, Dublin 8, Ireland
[2] St James Hosp, Dept Urol, Dublin 8, Ireland
关键词
intermittent androgen withdrawal; testosterone replacement; proliferation; biomarkers; HORMONE-THERAPY; CELL-LINE; RECEPTOR; GROWTH; EXPRESSION; HYPOXIA; INHIBITION; BICALUTAMIDE; WITHDRAWAL; OVEREXPRESSION;
D O I
10.1002/pros.21266
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Androgen deprivation therapy is initially successful in treating advanced prostate cancer. However, after a period of time tumors inevitably recur. Improved understanding of the various biochemical causes of resistance to hormonal therapy is of crucial importance for developing more effective therapeutic strategies in this cohort of patients. This review discusses the preclinical evidence for androgen hypersensitivity (AH), as a mechanism by which tumors become hormone-refractory (HR). We propose that the growth of some such tumors may be not only stimulated by, but also dependent on low hormone levels, and furthermore, that normal hormone concentrations can have an inhibitory effect on growth. The incidence and importance of AH merits further investigation both in preclinical studies and during clinical trials of intermittent androgen withdrawal or testosterone replacement. We suggest that a subset of HR prostate cancer patients who have androgen-hypersensitive tumors could be particularly amenable to these treatments. Finally, potential approaches for developing biomarkers to identify such patients are explored. Prostate 71: 550-557, 2011. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:550 / 557
页数:8
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