He. Jones et al., RESPONSE OF CELL-GROWTH AND RETINOIC ACID RECEPTOR EXPRESSION TO RETINOIC ACID IN NEOPLASTIC AND NONNEOPLASTIC PROSTATE CELL-LINES, The Prostate, 30(3), 1997, pp. 174-182
BACKGROUND. Retinoic acid (RA) is recognized as an inhibitor of tumori
genesis, but conversely, has also been shown to act as a tumor enhance
r, therefore its role in prostate tumor cell growth was investigated.
METHODS. The response of two human prostate tumor cell lines (PC-3 and
DU-145), and cell lines derived from a well-differentiated canine pro
state adenocarcinoma (CPA) and normal canine prostate epithelium (CAFE
) to all-trans RA was determined using growth curve analysis. Addition
ally, the constitutive expression and RA-challenged expression of reti
noic acid receptors (RARs) -alpha, -beta, and -gamma mRNA was examined
using Northern blotting techniques. RESULTS. In response to all-trans
RA, the PC-3 and DU-145 cell lines showed considerable growth promoti
on, while CAFE and CPA cell growth was dramatically inhibited. Each ce
ll line expressed RAR alpha and RAR gamma, with either negligible or n
o RAR beta transcripts being detected. RAR alpha and -gamma mRNAs dete
cted in the four cell lines were variably regulated in response to RA,
and no distinct patterns of RAR regulation that could be related to c
ell growth responses were observed. CONCLUSIONS. The data indicates th
at no simple association exists between the expression or regulation o
f RAR subtype mRNAs and the divergent growth responses to RA displayed
by the prostate cell lines. (C) 1997 Wiley-Liss, Inc.