The androgen receptor (AR) plays a critical role as a driver of castration-resistant prostate cancer (CRPC). Our previous studies demonstrated that disruption of transforming growth factor-β (TGF- β) signaling via introduction of dominant-negative transforming growth factor- β type II receptor (DNTGF βRII) in the prostate epithelium of transgenic adenocarcinoma of the prostate mice accelerated tumor. This study investigated the consequences of disrupted TGF- β signaling on prostate tumor growth under conditions of castration-induced androgen deprivation in the preclinical model of DNTGF βRII. Our results indicate that in response to androgen deprivation therapy (ADT) the proliferative index in prostate tumors from DNTGF βRII mice was higher compared with prostate tumors from TGF βRII wild-type (WT) mice, whereas there was a reduced incidence of apoptosis in tumors from DNTGF βRII. Protein and gene expression profiling revealed that tumors from DNTGF βRII mice exhibit a strong nuclear AR localization among the prostate tumor epithelial cells and increased AR messenger RNA after ADT. In contrast, TGF βRII WT mice exhibited a marked loss in nuclear AR in prostate tumor acini (20 weeks), followed by a downregulation of AR and transmembrane protease serine 2 messenger RNA. There was a significant increase in nuclear AR and activity in prostate tumors from castrate DNTGF βRII compared with TGF βRII WT mice. Consequential to aberrant TGF- β signaling, ADT enhanced expression and nuclear localization of Smad4 and β-catenin. Our findings support that under castrate conditions, aberrant TGF- β signaling leads to AR activation and β-catenin nuclear localization, an adaptation mechanism contributing to emergence of CRPC. The work defines a potentially significant new targeting platform for overcoming therapeutic resistance in CRPC.
This study examined the impact of TGF- β signaling on prostate cancer after castration in a mouse model. Prostate tumor adaptation to castrate androgen levels (via AR) promotes EMT and growth dynamics.