BACKGROUND. Urologists are looking for a way to easily discriminate be
tween aggressive and very slow-growing prostate tumors. A sound way to
appreciate such developing activities would be to identify an appropr
iate cell marker in prostate explants maintained in a defined culture
system. METHODS. Different biological parameters were compared in rat
prostate explants cultured for 5 days in rich CMRL or basic Leibovitz'
s L-15 medium, unsupplemented with serum, under a mixture of either 95
% air/5% CO2 or 50% N-2/45% O-2/5% CO2. RESULTS. DNA synthesis was som
ewhat similar with the two-gas combination, but was higher in explants
maintained in L-15 medium than in CMRL. Hence, L-15 medium and the 95
% air/5% CO2 mixture were selected. Under these defined conditions for
5 days, cells were still able to synthesize DNA and proteins while pr
eserving their morphological integrity and maintaining alkaline and ac
id phosphatase activities. CONCLUSIONS. Since the present culture syst
em works well in a controlled environment and under such minimal condi
tions, it appears to be a reliable and promising model that will provi
de basic data and allow the study of hormones and growth factors invol
ved in prostatic tissue growth. It might eventually permit the identif
ication of a cell marker. (C) 1997 Wiley-Liss, Inc.