Summary To assess the role of oestrogen regulation in the growth of ovarian cancer, we examined the effects of an oestrogen, 17 P-oestradiol, and an anti-oestrogen, tamoxifen, on oestrogen receptor (ER) -positive and -negative human ovarian carcinoma cell lines. As measured by a dextran-coated charcoal adsorption assay, cell lines PEOI, PEO4 (Schwartz et al., 1982;Pagel et al., 1983;Hamerlynck et al., 1985;Campbell et al., 1984), although others have failed to demonstrate such benefits Slevin et al., 1986;Shirey et al., 1984;Landoni et al., 1983).We have recently derived and characterized a series of human ovarian carcinoma cell lines (Langdon et al., 1988). In the present study, we measured the levels of ER in these lines and examined the effects of 17 P-oestradiol and the anti-oestrogen tamoxifen on the growth of two of these lines -the ER +ve line PE04 and the ER -ve line, PE014. We have also assessed the effects of high doses of tamoxifen on 8 of the lines of the series.
Materials and methods
Cell lines and drugsThe characterization of the cell lines has been described previously (Langdon et al., 1988) but brief details are recorded in Table I. Cell lines were routinely cultured at 37°C, 90% humidity and 5% CO2 in RPMI 1640 + fetal calf serum (FCS) (9:1) with streptomycin (100 gg ml-'), glutamine (2 mM), pyruvate (2 mM), penicillin (100 IU ml-'), and 3-[morpholino] propane sulphonic acid (12.5 mM, pH 7.4). 17 P-oestradiol was obtained from Sigma Ltd., Dorset, UK and tamoxifen was a gift from ICI Pharmaceuticals Ltd., Macclesfield, UK. In the cell growth experiments, both were initially dissolved in ethanol. The final concentration of ethanol in cell growth experiments was always less than 0.01 % v/v, a concentration previously shown to have no effect on these cell lines.Oestrogen receptor assays Assays were performed on cells which were in early plateau phase of their growth using the dextran-coated charcoal adsorption method described previously (Hawkins et al., 1975;Hawkins et al., 1981