Emerging mechanisms of enzalutamide resistance in prostate cancer

被引:116
作者
Claessens, Frank [1 ]
Helsen, Christine [1 ]
Prekovic, Stefan [1 ]
Van den Broeck, Thomas [1 ]
Spans, Lien [1 ]
Van Poppel, Hendrik [2 ]
Joniau, Steven [2 ]
机构
[1] Katholieke Univ Leuven, Dept Cellular & Mol, Mol Endocrinol Lab, B-3000 Louvain, Belgium
[2] Univ Hosp Leuven, Dept Dev & Regenerat, B-3000 Louvain, Belgium
关键词
ANDROGEN RECEPTOR VARIANTS; SPLICE VARIANTS; ANTIANDROGEN WITHDRAWAL; GROWTH; GLUCOCORTICOIDS; DEXAMETHASONE; ABIRATERONE; MUTATION; THERAPY; CELLS;
D O I
10.1038/nrurol.2014.243
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The majority of prostate cancers are hormone-dependent at diagnosis highlighting the central role of androgen signalling in this disease. Surprisingly, most forms of castration-resistant prostate cancer (CRPC) are still dependent on the androgen receptor (AR) for survival. Therefore, the advent of new AR-targeting drugs, such as enzalutamide, is certainly beneficial for the many patients with metastatic CRPC. Indeed, this compound provides a substantial survival benefit-but it is not curative. This Perspectives article describes the different ways through which cancer cells can become resistant to enzalutamide, such as AR truncation and other mutations, as well as by-pass of the AR dependence of prostate cancer cells through expression of the glucocorticoid receptor. The clinical relevance of these mechanisms and emerging questions concerning new therapeutic regimens in the treatment of metastatic CRPC are being discussed.
引用
收藏
页码:712 / 716
页数:5
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