beta-Catenin is a multifunctional molecule with important roles in intercel
lular adhesion and signal transduction. We reported previously that beta-ca
tenin is mutated in human prostate cancer. In this study, we investigated t
he role of beta-catenin mutations on androgen receptor (AR) signaling. beta
-Catenin significantly enhanced androgen-stimulated transcriptional activat
ion by the AR. beta-Catenin also increased AR transcriptional activation by
androstenedione and estradiol and diminished the antagonism of bicalutamid
e, Coimmunoprecipitation of beta-catenin with AR from LNCaP prostate cancer
cells showed that the two molecules are present in the same complex. The a
mount of beta-catenin in complex with AR was increased by androgen. These f
indings implicate beta-catenin in the regulation of AR function and support
a role for beta-catenin mutations in the pathogenesis of prostate cancer.