Antonarakis Emmanuel S
Prostate Cancer Research Program, Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA.
Expert Rev Anticancer Ther. 2015 Feb;15(2):143-5. doi: 10.1586/14737140.2015.999044. Epub 2014 Dec 30.
There is an emerging interest in understanding mechanisms of response and resistance to next-generation hormonal therapies: abiraterone and enzalutamide. While many explanations for resistance to these agents have been postulated, the importance of androgen receptor splice variants is gaining momentum. Androgen receptor (AR) splice variants are constitutively active isoforms of the AR that lack the ligand-binding domain yet retain their transcriptional activity in a ligand-independent fashion. Of these, AR variant-7 may be the most important, and has been implicated in primary resistance to abiraterone and enzalutamide in men with advanced prostate cancer. In this editorial, the clinical relevance of AR splice variant-7 (AR-V7) will be reviewed within the context of AR-directed therapies, and next steps for the analytical and clinical validation of this potential biomarker will be proposed.
人们对理解下一代激素疗法(阿比特龙和恩杂鲁胺)的反应和耐药机制的兴趣日益浓厚。虽然对这些药物耐药的许多解释已被提出,但雄激素受体剪接变体的重要性正日益凸显。雄激素受体(AR)剪接变体是AR的组成型活性异构体,缺乏配体结合域,但仍以不依赖配体的方式保留其转录活性。其中,AR变体-7可能是最重要的,并且已被认为与晚期前列腺癌男性对阿比特龙和恩杂鲁胺的原发性耐药有关。在这篇社论中,将在AR导向疗法的背景下回顾AR剪接变体-7(AR-V7)的临床相关性,并提出对这一潜在生物标志物进行分析和临床验证的下一步措施。