Chen Ze-Yu, Dong Qiang, Liu Liang-Ren, Wei Qiang
Research Institute of Urology / Department of Urology, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, China.
Zhonghua Nan Ke Xue. 2019 Feb;25(2):172-176.
As more and more patients with metastatic prostate cancer develop resistance to androgen-deprivation therapy (ADT) and consequently castration-resistant prostate cancer (CRPC), reasonable selection of therapies is becoming increasingly important for the prediction of the therapeutic results. Many studies show that androgen receptor splice variant 7 (AR-V7) is involved in the development and progression of CRPC and that the expression of AR-V7, absolutely higher in CRPC than in hormone-nave prostate cancer, plays a significant role in the mechanisms of resistance to abiraterone, enzalutamide and taxane chemotherapies. Further more, some clinical trials have revealed that the AR-V7 level may indicate the prognosis of different therapeutic options: AR-V7 negative in circulating tumor cells suggesting the effectiveness of a new hormonal therapy and taxane chemotherapy while AR-V7 positive indicating the poor result of a new hormonal therapy. These findings show that AR-V7 could be a biomarker for therapeutic options and the prognostic evaluation of CRPC.
随着越来越多的转移性前列腺癌患者对雄激素剥夺疗法(ADT)产生耐药性,进而发展为去势抵抗性前列腺癌(CRPC),合理选择治疗方法对于预测治疗效果变得越来越重要。许多研究表明,雄激素受体剪接变体7(AR-V7)参与CRPC的发生和发展,并且AR-V7的表达在CRPC中绝对高于激素初治前列腺癌,在对阿比特龙、恩杂鲁胺和紫杉烷化疗的耐药机制中起重要作用。此外,一些临床试验表明,AR-V7水平可能预示不同治疗方案的预后:循环肿瘤细胞中AR-V7阴性表明新的激素疗法和紫杉烷化疗有效,而AR-V7阳性表明新的激素疗法效果不佳。这些发现表明,AR-V7可能是CRPC治疗方案和预后评估的生物标志物。