Cancer Therapy: Preclinical Resistance to CYP17A1 Inhibition with Abiraterone in Castration-Resistant Prostate Cancer: Induction of Steroidogenesis and Androgen Receptor Splice Variants

Purpose: Abiraterone is a potent inhibitor of the steroidogenic enzyme CYP17A1 and suppresses tumor growth in patients with castration-resistant prostate cancer (CRPC). The effectiveness of abiraterone in reducing tumor androgens is not known, nor havemechanisms contributing to abiraterone resistance been established. Experimental Design: We treated human CRPC xenografts with abiraterone and measured tumor growth, tissue androgens, androgen receptor (AR) levels, and steroidogenic gene expression versus controls. Results: Abiraterone suppressed serum PSA levels and improved survival in two distinct CRPC xenografts: median survival of LuCaP35CR improved from 17 to 39 days (HR 1⁄4 3.6, P 1⁄4 0.0014) and LuCaP23CR from14 to 24 days (HR1⁄4 2.5, P1⁄4 0.0048). Abiraterone strongly suppressed tumor androgens, with testosterone (T) decreasing from 0.49 0.22 to 0.03 0.01 pg/mg (P < 0.0001), and from 0.69 0.36 to 0.03 0.01 pg/mg (P 1⁄4 0.002) in abiraterone-treated 23CR and 35CR, respectively, with comparable decreases in tissue DHT. Treatment was associated with increased expression of full-length AR (AR) and truncated AR variants (AR 2.3-fold, P1⁄4 0.008 and AR 2.7-fold, P1⁄4 0.036 in 23 CR; AR 3.4-fold, P 1⁄4 0.001 and AR 3.1-fold, P 1⁄4 0.0003 in 35CR), and increased expression of the abiraterone target CYP17A1 ( 2.1-fold, P 1⁄4 0.0001 and P 1⁄4 0.028 in 23CR and 35CR, respectively) and transcript changes in other enzymes modulating steroid metabolism. Conclusions: These studies indicate that abiraterone reduces CRPC growth via suppression of intratumoral androgens and that resistance to abiraterone may occur through mechanisms that include upregulation of CYP17A1, and/or induction of AR and AR splice variants that confer ligand-independent AR transactivation. Clin Cancer Res; 17(18); 5913–25. 2011 AACR.