Henttu P, Liao S S, Vihko P
Biocenter, University of Oulu, Finland.
Endocrinology. 1992 Feb;130(2):766-72. doi: 10.1210/endo.130.2.1370795.
To better understand androgen-regulated gene expression in the prostate, we have used Northern blot analysis to study the effects of androgens and other steroid hormones on the steady state levels of several human prostatic mRNAs in the LNCaP cell line. Dihydrotestosterone (40 nM) as well as a synthetic androgen, R1881 (0.1 nM), increased the amounts of prostate-specific antigen (PSA) and human glandular kallikrein mRNAs; at the same time, the level of prostatic acid phosphatase (PAP) mRNA was down-regulated. Incubation of LNCaP cells with medium containing 0.1 or 1 microM R1881 for 3, 7, or 13 days resulted in up-regulation of PSA and human glandular kallikrein mRNAs and down-regulation of PAP mRNA. Thus, the two clinically important prostate-specific marker proteins are inversely regulated in this cell line. The level of human androgen receptor mRNA was also repressed by the androgen treatments. 17 beta-Estradiol and progesterone had effects similar to those of R1881 on gene expression in LNCaP cells. Our results show that the decrease in the amount of secreted PAP and the increase in the amount of secreted PSA caused by androgens and other steroid hormones in the LNCaP cells of epithelial origin are mediated by changes in the levels of the corresponding mRNAs.
为了更好地理解雄激素对前列腺中基因表达的调控作用,我们运用Northern印迹分析技术,研究了雄激素及其他类固醇激素对LNCaP细胞系中几种人类前列腺mRNA稳态水平的影响。双氢睾酮(40 nM)以及合成雄激素R1881(0.1 nM)均可增加前列腺特异性抗原(PSA)和人腺激肽释放酶mRNA的量;与此同时,前列腺酸性磷酸酶(PAP)mRNA的水平则下调。将LNCaP细胞在含有0.1或1 microM R1881的培养基中孵育3、7或13天,会导致PSA和人腺激肽释放酶mRNA上调,而PAP mRNA下调。因此,在该细胞系中,这两种临床上重要的前列腺特异性标志物蛋白受到相反的调控。雄激素处理也会抑制人雄激素受体mRNA的水平。17β-雌二醇和孕酮对LNCaP细胞中的基因表达具有与R1881类似的作用。我们的结果表明,在上皮来源的LNCaP细胞中,雄激素及其他类固醇激素导致分泌的PAP量减少和分泌的PSA量增加,这是由相应mRNA水平的变化介导的。