In the present study, the role of BRCA1 in Ligand-dependent androgen recept
or (AR) signaling was assessed, In transfected prostate and breast cancer c
ell lines, BRCA1 enhanced AR-dependent transactivation of a probasin-derive
d reporter gene. The effects of BRCA1 were mediated through the NH2-termina
l activation function (AF-I) of the receptor, Cotransfection of p160 coacti
vators markedly potentiated BRCB1-mediated enhancement of AR signaling, In
addition, BRCA1 was shown to interact physically with both the AR and the p
160 coactivator, glucacorticoid receptor interacting protein 1. These findi
ngs suggest that BRCA1 may directly modulate BR signaling and, therefore, m
ay have implications regarding the proliferation of normal and malignant an
drogen-regulated tissues.