A novel androgen receptor antagonist JJ-450 inhibits enzalutamide-resistant mutant ARF876L nuclear import and function

Background Castration-resistant prostate cancer can develop resistance to enzalutamide because of androgen receptor (AR) point mutations, AR overexpression, constitutively active AR splice variants, and/or elevated intratumoral androgen synthesis. The point mutation AR(F876L) was reported to be stimulated, instead of inhibited, by enzalutamide, thus contributing to enzalutamide resistance. We have recently developed JJ-450 as a novel AR antagonist with the potential to treat enzalutamide-resistant castration-resistant prostate cancer (CRPC). Methods We employed several assays to determine the impact of JJ-450 and enzalutamide on prostate cancer cell lines expressing green fluorescent protein (GFP)-AR(F876L). These assays include a prostate-specific antigen enhancer/promoter-based luciferase assay to determine AR transcriptional activity, a quantitative real-time polymerase chain reaction assay, and Western blot analysis to detect expression of AR-target genes at the messenger RNA and protein level, fluorescence microscopy to show AR subcellular localization, and a 5-bromo-2 '-deoxyuridine assay to measure prostate cancer cell proliferation. Results As expected, enzalutamide inhibited wild-type (WT) AR but not AR(F876L) transcriptional activity in the luciferase assay. In contrast, JJ-450 inhibited both WT-AR and AR(F876L) transcriptional activity to a similar extent. Also, enzalutamide retarded androgen-induced nuclear import of GFP-AR, but not GFP-AR(F876L), whereas JJ-450 retarded nuclear import of both GFP-AR and GFP-AR(F876L). To further evaluate JJ-450 inhibition of AR(F876L), we stably transfected C4-2 cells separately with GFP-AR or GFP-AR(F876L). Enzalutamide inhibited endogenous AR-target gene expression in C4-2-GFP-AR(WT), but not in the C4-2-GFP-AR(F876L) subline, whereas JJ-450 inhibited AR-target gene expression in both C4-2 sublines. More importantly, enzalutamide inhibited proliferation of C4-2-GFP-AR(WT), but not of the C4-2-GFP-AR(F876L) subline, whereas JJ-450 inhibited proliferation of both C4-2 sublines. Conclusion JJ-450 inhibits enzalutamide-resistant AR(F876L) mutant nuclear translocation and function. Our findings suggest that JJ-450 and its analogs should be further developed to provide a potential new approach for the treatment of enzalutamide-resistant CRPC.