Welti Jonathan, Rodrigues Daniel Nava, Sharp Adam, Sun Shihua, Lorente David, Riisnaes Ruth, Figueiredo Ines, Zafeiriou Zafeiris, Rescigno Pasquale, de Bono Johann S, Plymate Stephen R
Prostate Cancer Targeted Therapy Group, Institute of Cancer Research and The Royal Marsden NHS Foundation Trust, Sutton, UK.
Department of Medicine, University of Washington School of Medicine and VAPSHCS-GRECC, Seattle, WA, USA.
Eur Urol. 2016 Oct;70(4):599-608. doi: 10.1016/j.eururo.2016.03.049. Epub 2016 Apr 23.
The androgen receptor splice variant-7 (AR-V7) has been implicated in the development of castration-resistant prostate cancer (CRPC) and resistance to abiraterone and enzalutamide.
To develop a validated assay for detection of AR-V7 protein in tumour tissue and determine its expression and clinical significance as patients progress from hormone-sensitive prostate cancer (HSPC) to CRPC.
DESIGN, SETTING, AND PARTICIPANTS: Following monoclonal antibody generation and validation, we retrospectively identified patients who had HSPC and CRPC tissue available for AR-V7 immunohistochemical (IHC) analysis.
Nuclear AR-V7 expression was determined using IHC H score (HS) data. The change in nuclear AR-V7 expression from HSPC to CRPC and the association between nuclear AR-V7 expression and overall survival (OS) was determined.
Nuclear AR-V7 expression was significantly lower in HSPC (median HS 50, interquartile range [IQR] 17.5-90) compared to CRPC (HS 135, IQR 80-157.5; p<0.0001), and in biopsy tissue taken before (HS 80, IQR 30-136.3) compared to after (HS 140, IQR 105-167.5; p=0.007) abiraterone or enzalutamide treatment. Lower nuclear AR-V7 expression at CRPC biopsy was associated with longer OS (hazard ratio 1.012, 95% confidence interval 1.004-1.020; p=0.003). While this monoclonal antibody primarily binds to AR-V7 in PC biopsy tissue, it may also bind to other proteins.
We provide the first evidence that nuclear AR-V7 expression increases with emerging CRPC and is prognostic for OS, unlike antibody staining for the AR N-terminal domain. These data indicate that AR-V7 is important in CRPC disease biology; agents targeting AR splice variants are needed to test this hypothesis and further improve patient outcome from CRPC.
In this study we found that levels of the protein AR-V7 were higher in patients with advanced prostate cancer. A higher level of AR-V7 identifies a group of patients who respond less well to certain prostate cancer treatments and live for a shorter period of time.
雄激素受体剪接变体7(AR-V7)与去势抵抗性前列腺癌(CRPC)的发生以及对阿比特龙和恩杂鲁胺的耐药性有关。
开发一种经过验证的检测肿瘤组织中AR-V7蛋白的方法,并确定其在患者从激素敏感性前列腺癌(HSPC)进展为CRPC过程中的表达及临床意义。
设计、设置和参与者:在产生并验证单克隆抗体后,我们回顾性确定了有HSPC和CRPC组织可用于AR-V7免疫组织化学(IHC)分析的患者。
使用IHC H评分(HS)数据确定细胞核AR-V7表达。确定从HSPC到CRPC细胞核AR-V7表达的变化以及细胞核AR-V7表达与总生存期(OS)之间的关联。
与CRPC(HS 135,四分位间距[IQR] 80 - 157.5;p<0.0001)相比,HSPC中细胞核AR-V7表达显著更低(中位数HS 50,IQR 17.5 - 90),与阿比特龙或恩杂鲁胺治疗后(HS 140,IQR 105 - 167.5;p = 0.007)相比,治疗前活检组织中(HS 80,IQR 30 - 136.3)的表达更低。CRPC活检时较低的细胞核AR-V7表达与更长的OS相关(风险比1.012,95%置信区间1.004 - 1.020;p = 0.003)。虽然这种单克隆抗体主要与PC活检组织中的AR-V7结合,但它也可能与其他蛋白质结合。
我们提供了首个证据,即与AR N端结构域的抗体染色不同,细胞核AR-V7表达随着CRPC的出现而增加,并且对OS具有预后价值。这些数据表明AR-V7在CRPC疾病生物学中很重要;需要靶向AR剪接变体的药物来验证这一假设并进一步改善CRPC患者的预后。
在本研究中,我们发现晚期前列腺癌患者中AR-V7蛋白水平更高。AR-V7水平较高可识别出一组对某些前列腺癌治疗反应较差且生存期较短的患者。