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首页> 外文期刊>Biochemical and Biophysical Research Communications >Ghrelin inhibits proliferation and increases T-type Ca2+ channel expression in PC-3 human prostate carcinoma cells.
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Ghrelin inhibits proliferation and increases T-type Ca2+ channel expression in PC-3 human prostate carcinoma cells.

机译:Ghrelin抑制PC-3人前列腺癌细胞中的增殖并增加T型Ca2 +通道表达。

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Ghrelin is a multifunctional peptide hormone with roles in growth hormone release, food intake and cell proliferation. With ghrelin now recognized as important in neoplastic processes, the aim of this report is to present findings from a series of in vitro studies evaluating the cellular mechanisms involved in ghrelin regulation of proliferation in the PC-3 human prostate carcinoma cells. The results showed that ghrelin significantly decreased proliferation and induced apoptosis. Consistent with a role in apoptosis, an increase in intracellular free Ca(2+) levels was observed in the ghrelin-treated cells, which was accompanied by up-regulated expression of T-type voltage-gated Ca(2+) channels. Interestingly, T-channel antagonists were able to prevent the effects of ghrelin on cell proliferation. These results suggest that ghrelin inhibits proliferation and may promote apoptosis by regulating T-type Ca(2+) channel expression.
机译:Ghrelin是一种多功能肽激素,在生长激素释放,食物摄入和细胞增殖中起作用。 ghrelin现在被认为在肿瘤形成过程中很重要,因此本报告的目的是提供一系列体外研究的结果,这些研究评估了ghrelin调节PC-3人前列腺癌细胞增殖的细胞机制。结果表明,生长素释放肽显着降低增殖并诱导凋亡。与凋亡中的作用一致,在生长激素释放肽处理的细胞中观察到细胞内游离Ca(2+)水平的增加,同时伴随着T型电压门控Ca(2+)通道的表达上调。有趣的是,T通道拮抗剂能够预防Ghrelin对细胞增殖的影响。这些结果表明,ghrelin抑制增殖,并可能通过调节T型Ca(2+)通道表达来促进细胞凋亡。

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