AIM: To study the molecular mechanism of rat prostate atrophy induced by ep
risteride. METHODS: MTT test was used to determine the effect of epristerid
e on the growth of prostatic epithelial cell induced by exogenous epithelia
l growth factor (EGF) or insulin-like growth factor-I (IGF-I). RT-PCR and f
low cytometry were then used to quantitatively detect the mRNA and protein
expressions of EGFR and IGF-I R of the epithelial cells treated or untreate
d with epristeride. RESULTS: Epristeride attenuated growth of epithelial ce
lls induced by exogenous EGF, IGF-I. Epristeride 360 nmol/L inhibited EGFR
and IGF-I R expression at mRNA level, while epristeride 180 nmol/L had no m
arked effect on EGFR and IGF-I R mRNA expression. Both epristeride 180 nmol
/L and 360 nmol/L could down regulate EGFR and IGF-IR protein levels. CONCL
USION: The molecular mechanisms of prostatic epithelial cell atrophy induce
d by epristeride might be associated with alteration in the expression of g
rowth factor receptors such as EGF and IGF-I.