We used three heterogeneous parental cultures of LSC-AXC rat prostate cancer cells: LSC-AXC-C/0, cells maintained on culture medium; LSC-AXC-D/0, cells maintained on culture medium containing 10-7m 5α-dihydrotestosterone; and LSC-AXC-T/0, cells maintained on culture medium containing 10-7m testosterone, to isolate clonally derived cell lines. Eleven of 15 clonal cell lines were tumorigenic when inoculated into intact male AXC rats. Eight tumorigenic clonal cell lines were selected for further evaluation, and all were found to possess features characteristic of secretory epithelium, as judged by light and electron microscopy. All parental cell lines and the eight selected clonal cell lines contained cytoplasmic and nuclear androgen receptors. Total receptor content was 131 ± 61 (S.D.), 43 ± 32, and 274 ± 96 fmol/100 µg of DNA, respectively, for C-, D-, and T-cells. The differences were significant (p < 0.05). Androgen receptor content of young mature or senescent AXC rat ventral prostate, respectively, is 518 ± 58 and 266 ± 40 fmol/100 µg of DNA. Since chromosomal analysis established that LSC-AXC prostate cancer cells are hypotriploid, androgen receptor content per cell in C- and T-cells is indicated to be either greater than or equal to that of senescent AXC rat ventral prostate, the tissue in which the original adenocarcinoma arose. Parental and clonal cell lines contained 5α-reductase activity. There were significant differences (p < 0.05) in both total reductase activity and metabolite distribution. Consequently, the intracellular content of testosterone metabolites was cell line specific. All characterized cell lines contained a higher concentration (p < 0.05) of APase activity than did young mature or senescent AXC rat ventral prostate. In 6 of 11 cell lines, prostate-secretory APase concentration exceeded (p < 0.05) that of AXC rat ventral prostate. However, the relative content of secretory APase compared to total APase in carcinoma cells consistently was less (p < 0.05) than that of AXC rat ventral prostate. These studies document the establishment of clonal AXC rat prostate adenocarcinoma cell lines which have retained important morphological and phenotypic markers characteristic of differentiated prostate epithelium. Since these cells are tumorigenic and represent a spectrum of retained differentiated phenotypic markers, they should be particularly useful for in vivo and in vitro studies of hormonal regulation of prostate cancer cell behavior.

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Supported in part by Grant CA-30116 from the National Cancer Institute, Department of Health and Human Services.

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