Department of Medicine, Section of Epidemiology and Population Sciences, Baylor College of Medicine, Houston, TX 77030, USA.
Department of Biology and Biochemistry, University of Bath, Bath BA2 7AY, UK.
Int J Mol Sci. 2021 May 24;22(11):5515. doi: 10.3390/ijms22115515.
Metastatic prostate cancer is the most common cancer in males and the fifth cause of cancer mortality worldwide. Despite the major progress in this field, leading to the approval of novel anti-androgens, the prognosis is still poor. A significant number of patients acquire an androgen receptor splice variant 7 (AR-V7), which is constitutively activated and lacks the ligand-binding domain (LBD) while maintaining the nuclear localization signal and DNA-binding domain (DBD). This conformational change, even in the absence of the ligand, allows its retention within the nucleus, where it acts as a transcription factor repressing crucial tumor suppressor genes. AR-V7 is an important oncogenic driver and plays a role as an early diagnostic and prognostic marker, as well as a therapeutic target for antagonists such as niclosamide and TAS3681. Anti-AR-V7 drugs have shown promise in recent clinical investigations on this subset of patients. This mini-review focuses on the relevance of AR-V7 in the clinical manifestations of castration-resistant prostate cancer (CRPC) and summarizes redemptive therapeutic strategies.
转移性前列腺癌是男性最常见的癌症,也是全球第五大癌症死亡原因。尽管在这一领域取得了重大进展,批准了新型抗雄激素药物,但预后仍然不佳。相当数量的患者会产生雄激素受体剪接变异体 7(AR-V7),其持续激活且缺乏配体结合域(LBD),同时保留核定位信号和 DNA 结合域(DBD)。这种构象变化,即使没有配体,也能使其保留在核内,在核内作为转录因子抑制关键的肿瘤抑制基因。AR-V7 是一个重要的致癌驱动因子,作为早期诊断和预后标志物,以及拮抗剂如尼氯硝唑和 TAS3681 的治疗靶点发挥作用。针对这部分患者的最近的临床研究表明,抗 AR-V7 药物具有良好的应用前景。本综述聚焦于 AR-V7 在去势抵抗性前列腺癌(CRPC)临床表现中的相关性,并总结了有前途的治疗策略。