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雄激素对人前列腺癌细胞系LNCaP中编码地西泮结合抑制剂/酰基辅酶A结合蛋白的信使核糖核酸的调控。

Androgen regulation of the messenger RNA encoding diazepam-binding inhibitor/acyl-CoA-binding protein in the human prostatic adenocarcinoma cell line LNCaP.

作者信息

Swinnen J V, Esquenet M, Heyns W, Rombauts W, Verhoeven G

机构信息

Laboratory for Experimental Medicine and Endocrinology, Faculty of Medicine, Catholic University of Leuven, Belgium.

出版信息

Mol Cell Endocrinol. 1994 Sep;104(2):153-62. doi: 10.1016/0303-7207(94)90118-x.

Abstract

To study the mechanisms by which androgens intervene in the regulation of growth and differentiation of human prostatic epithelial cells, cDNA clones encoding putative prostate-secreted proteins were characterized and tested as potential markers for androgen action. One of the isolated cDNAs expressed diazepam-binding inhibitor/acyl-CoA-binding protein (DBI/ACBP), suggesting that this polypeptide, that has been implicated in a large number of biochemical processes, is expressed and secreted by prostate cells. As demonstrated by Northern blot analysis, the mRNA encoding DBI/ACBP was expressed in prostate tissue and in the three human prostatic adenocarcinoma cell lines tested: LNCaP, PC-3 and DU-145. In androgen-sensitive LNCaP cells, the synthetic androgen R1881 stimulated the DBI/ACBP steady state mRNA levels with half maximal effects at a concentration of 0.2 nM. Increases were a maximal 12 h after addition of the synthetic hormone. DBI/ACBP mRNA levels could also be stimulated by the synthetic androgen mibolerone and by the natural androgens testosterone and dihydrotestosterone. In agreement with the altered steroid specificity of the androgen receptor in LNCaP cells, estradiol and progesterone also exerted a stimulatory effect. Cortisol and the synthetic glucocorticoid dexamethasone were without effect. Androgen stimulation of DBI/ACBP mRNA levels was abolished in the presence of the protein synthesis inhibitor cycloheximide, implying a role for labile or androgen-induced proteins in this androgen stimulation. This is in contrast to the androgen stimulation of the mRNA encoding prostate-specific antigen (PSA), suggesting that different mechanisms are involved in the androgen regulation of these two genes. Although further experiments are required to confirm that DBI/ACBP is secreted by prostatic epithelial cells, these data demonstrate that the mRNA encoding DBI/ACBP is expressed in prostate cells and is affected by androgens in androgen-responsive LNCaP cells.

摘要

为研究雄激素干预人类前列腺上皮细胞生长和分化调节的机制,对编码假定前列腺分泌蛋白的cDNA克隆进行了表征,并将其作为雄激素作用的潜在标志物进行测试。分离出的一个cDNA表达地西泮结合抑制剂/酰基辅酶A结合蛋白(DBI/ACBP),这表明这种涉及大量生化过程的多肽由前列腺细胞表达和分泌。Northern印迹分析表明,编码DBI/ACBP的mRNA在前列腺组织以及所测试的三种人类前列腺腺癌细胞系:LNCaP、PC-3和DU-145中表达。在雄激素敏感的LNCaP细胞中,合成雄激素R1881刺激DBI/ACBP稳态mRNA水平,在浓度为0.2 nM时产生半数最大效应。添加合成激素后最大增加在12小时出现。DBI/ACBP mRNA水平也可被合成雄激素米勃龙以及天然雄激素睾酮和双氢睾酮刺激。与LNCaP细胞中雄激素受体改变的类固醇特异性一致,雌二醇和孕酮也发挥刺激作用。皮质醇和合成糖皮质激素地塞米松无作用。在存在蛋白质合成抑制剂环己酰亚胺的情况下,雄激素对DBI/ACBP mRNA水平的刺激作用被消除,这意味着不稳定或雄激素诱导的蛋白质在这种雄激素刺激中起作用。这与雄激素对编码前列腺特异性抗原(PSA)的mRNA的刺激作用形成对比,表明这两个基因的雄激素调节涉及不同机制。尽管需要进一步实验来证实DBI/ACBP由前列腺上皮细胞分泌,但这些数据表明编码DBI/ACBP的mRNA在前列腺细胞中表达,并在雄激素反应性LNCaP细胞中受雄激素影响。

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