Targeting the androgen receptor in prostate cancer

被引:39
作者
Culig, Zoran [1 ]
机构
[1] Med Univ Innsbruck, Dept Urol, A-6020 Innsbruck, Austria
关键词
androgen receptor; chemotherapy; prostate cancer; steroidogenesis; SUPPRESSES CASTRATION-RESISTANT; PROTEIN-BINDING PROTEIN; ABIRATERONE ACETATE; SPLICE VARIANTS; ENZALUTAMIDE RESISTANCE; ANTITUMOR-ACTIVITY; GENE-EXPRESSION; FULL-LENGTH; LNCAP CELLS; IN-VITRO;
D O I
10.1517/14656566.2014.915313
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: The androgen receptor (AR) is a ligand-activated transcription factor that is expressed in primary and metastatic prostate cancers. There are advances in endocrine therapy for prostate cancer that are based on improved understanding of AR function. Areas covered: PubMed has been used to include most important publications on targeting the AR in prostate cancer. AR expression may be downregulated by agents used for chemoprevention of prostate cancer or, in models of advanced prostate cancer, by antisense oligonucleotides. New drugs that inhibit the steroidogenic enzyme CYP17A1 (abiraterone acetate) or diminish nuclear translocation of the AR (enzalutamide) have been shown to improve patients' survival in prostate cancer. However, it is clear that there is a development of resistance to these novel therapies. They may include increased expression of truncated, constitutively active AR or activation of the signaling pathway of signal transducers and activators of transcription. Expert opinion: Although introduction of novel drugs have improved patients' survival, there is a need to investigate the mechanisms of resistance further. The role of truncated AR and compensatory activation of signaling pathways as well as the development of scientifically justified combination therapies seems to be issues of a high priority.
引用
收藏
页码:1427 / 1437
页数:11
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