Targeting the N-Terminal Domain of the Androgen Receptor: A New Approach for the Treatment of Advanced Prostate Cancer

被引:54
|
作者
Antonarakis, Emmanuel S. [1 ,2 ]
Chandhasin, Chandtip [3 ]
Osbourne, Erica [3 ]
Luo, Jun [2 ]
Sadar, Marianne D. [4 ]
Perabo, Frank [3 ]
机构
[1] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr, 1650 Orleans St,CRB1-1M45, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, James Buchanan Brady Urol Inst, Dept Urol, Baltimore, MD USA
[3] ESSA Pharmaceut Corp, Houston, TX USA
[4] BC Canc Agcy, Vancouver, BC, Canada
来源
ONCOLOGIST | 2016年 / 21卷 / 12期
基金
美国国家卫生研究院;
关键词
EPI-506; Androgen receptor; N-terminal domain; Prostate cancer; IN-SITU HYBRIDIZATION; BET BROMODOMAIN PROTEINS; ABIRATERONE ACETATE; CLINICAL ACTIVITY; SPLICE VARIANTS; SMALL-MOLECULE; TRANSCRIPTIONAL ACTIVATION; ANTITUMOR-ACTIVITY; INCREASED SURVIVAL; ENZALUTAMIDE;
D O I
10.1634/theoncologist.2016-0161
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite the recent approval and widespread use of abiraterone acetate and enzalutamide for the treatment of castration resistant prostate cancer (CRPC), this disease still poses significant management challenges because of various tumor escape mechanisms, including those that allow androgen receptor (AR) signaling to remain active.These AR-related resistance mechanisms include AR gene amplification or over expression, constitutively active ligand-independent AR splice variants, and gain-of-function mutations involving the AR ligandbinding domain (LBD), among others. Therefore, the development of AR-targeted therapies that function independently of the LBD represents an unmet medical need and has the potential to overcome many of these resistance mechanisms. This article discusses N-terminal domain (NTD) inhibition as a novel concept in the field of AR-directed therapies for prostate cancer. AR NTD-targeting agents have the potential to overcome shortcomings of current hormonal therapies by inhibiting all forms of AR-mediated transcriptional activity, and as a result, may affect a broader AR population including mutational and splice variant ARs. Indeed, the first clinical trial of an AR NTD inhibitor is now underway.
引用
收藏
页码:1427 / 1435
页数:9
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