Ghrelin inhibits proliferation and increases T-type Ca2+ channel expression in PC-3 human prostate carcinoma cells

被引:48
作者
Diaz-Lezama, Nundehui [1 ]
Hernandez-Elvira, Mariana [1 ]
Sandoval, Alejandro [2 ]
Monroy, Alma [3 ]
Felix, Ricardo [3 ]
Monjaraz, Eduardo [1 ]
机构
[1] Autonomous Univ Puebla BUAP, Inst Physiol, Neuroendocrinol Lab, Puebla, Mexico
[2] Natl Autonomous Univ Mexico UNAM, Sch Med FES Iztacala, Tlalnepantla, Mexico
[3] Natl Polytech Inst Cinvestav IPN, Dept Cell Biol, Ctr Res & Adv Studies, Mexico City, DF, Mexico
关键词
Ca2+ channels; Ca(v)3 channels; Ghrelin; Mibefradil; Pimozide; Prostate cancer; GROWTH-HORMONE SECRETAGOGUES; BIOLOGICAL-ACTIVITY; CANCER; RECEPTORS; PEPTIDE;
D O I
10.1016/j.bbrc.2010.10.100
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 Ca2+ levels was observed in the ghrelin-treated cells, which was accompanied by up-regulated expression of T-type voltage-gated Ca2+. 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 Ca2+ channel expression. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:24 / 29
页数:6
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