Lin M F, Lee M S, Garcia-Arenas R, Lin F F
Department of Biochemistry and Molecular Biology, College of Medicine, University of Nebraska Medical Center, Omaha 68198, USA.
Cell Biol Int. 2000;24(10):681-9. doi: 10.1006/cbir.2000.0433.
Androgens regulate the expression of both human prostatic acid phosphatase (PAcP) and prostate-specific antigen (PSA), two major prostate epithelium-specific differentiation antigens. Due to the important role of these two enzymes as prostate epithelium differentiation markers, we investigated their regulation of expression at the mRNA level in LNCaP human prostate carcinoma cells. Interestingly, phenol red, a pH indicator in the culture medium, promoted cell growth. To eliminate this non-specific effect, a phenol red-free, steroid-reduced medium was utilized. When high-density cells were grown in that medium, 5alpha-dihydrotestosterone (DHT) suppressed PAcP but stimulated PSA. However, tumor promoter phorbol ester 12-o-tetradecanoyl phorbol-13-acetate (TPA) functioned as a potent inhibitor of both PAcP and PSA expression. Prolonged treatment with DHT as well as TPA resulted in a similar down-regulation of protein kinase C and cellular PAcP activities. Thus, the levels of PAcP and PSA mRNA are differentially regulated by androgens in LNCaP cells.
雄激素调节人前列腺酸性磷酸酶(PAcP)和前列腺特异性抗原(PSA)这两种主要的前列腺上皮特异性分化抗原的表达。由于这两种酶作为前列腺上皮分化标志物的重要作用,我们研究了它们在LNCaP人前列腺癌细胞中mRNA水平的表达调控。有趣的是,培养基中的pH指示剂酚红促进细胞生长。为消除这种非特异性作用,使用了不含酚红、降低类固醇的培养基。当高密度细胞在该培养基中生长时,5α-二氢睾酮(DHT)抑制PAcP但刺激PSA。然而,肿瘤促进剂佛波酯12-O-十四烷酰佛波醇-13-乙酸酯(TPA)是PAcP和PSA表达的有效抑制剂。用DHT以及TPA长期处理导致蛋白激酶C和细胞PAcP活性类似的下调。因此,LNCaP细胞中PAcP和PSA mRNA的水平受雄激素的差异调节。