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首页> 外文期刊>Molecular and Cellular Endocrinology >Transcriptional regulation of type 11 17beta-hydroxysteroid dehydrogenase expression in prostate cancer cells.
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Transcriptional regulation of type 11 17beta-hydroxysteroid dehydrogenase expression in prostate cancer cells.

机译:前列腺癌细胞中11型17β-羟类固醇脱氢酶表达的转录调控。

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摘要

Type 11 hydroxysteroid (17-beta) dehydrogenase (HSD17B11) catalyzes the conversion of 5alpha-androstan-3alpha,17beta-diol into androsterone suggesting that it may play an important role in androgen metabolism. We previously described that overexpression of C/EBPalpha or C/EBPbeta induced HSD17B11 expression in HepG2 cells but this process was not mediated by the CCAAT boxes located within its proximal promoter region. Here, we study HSD17B11 transcriptional regulation in prostate cancer (PC) cells. Transfection experiments showed that the region -107/+18 is sufficient for promoter activity in PC cells. Mutagenesis analysis indicated that Sp1 and C/EBP binding sites found in this region are essential for promoter activity. Additional experiments demonstrated that ectopic expression of Sp1 and C/EBPalpha upregulated HSD17B11 expression only in PC cell lines. Through DAPA and ChIP assays, specific recruitment of Sp1 and C/EBPalpha to the HSD17B11 promoter was detected. These results show that HSD17B11 transcription in PC cells is regulated by Sp1 and C/EBPalpha.
机译:11型羟类固醇(17-beta)脱氢酶(HSD17B11)催化5alpha-androstan-3alpha,17beta-二醇转化为雄甾酮,表明它可能在雄激素代谢中起重要作用。我们以前描述过,C / EBPalpha或C / EBPbeta的过表达诱导了HepG2细胞中HSD17B11的表达,但是该过程不是由位于其近端启动子区域内的CCAAT框介导的。在这里,我们研究前列腺癌细胞(PC)细胞中的HSD17B11转录调控。转染实验表明,-107 / + 18区足以满足PC细胞中的启动子活性。诱变分析表明,在该区域发现的Sp1和C / EBP结合位点对于启动子活性至关重要。其他实验表明,Sp1和C / EBPalpha的异位表达仅在PC细胞系中上调HSD17B11表达。通过DAPA和ChIP分析,检测到Sp1和C / EBPalpha特异性募集到HSD17B11启动子。这些结果表明PC细胞中的HSD17B11转录受Sp1和C / EBPalpha调控。

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