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硝苯地平与钙协同作用激活钙敏感受体,抑制胸苷酸合成酶和存活素的表达,增强人结肠癌细胞对氟尿嘧啶的敏感性。

Nifedipine synergizes with calcium in activating the calcium sensing receptor, suppressing the expression of thymidylate synthase and survivin and promoting sensitivity to fluorouracil in human colon carcinoma cells.

机构信息

Simmons Cancer Institute, Southern Illinois University School of Medicine, Springfield, Illinois 62794-9677, USA.

出版信息

Mol Carcinog. 2011 Dec;50(12):922-30. doi: 10.1002/mc.20752. Epub 2011 Mar 3.

DOI:10.1002/mc.20752
PMID:21374737
Abstract

We have previously reported that activation of the G protein coupled calcium-sensing receptor (CaSR) by extracellular Ca(2+) down-modulates the expression of thymidylate synthase (TS) and survivin and promotes sensitivity to fluorouracil in human colon carcinoma cells. Here, we report for the first time that the cardiac drug nifedipine acted synergistically with Ca(2+) in CaSR activation and in the induction of intracellular Ca(2+). Nifedipine in combination with Ca(2+) significantly down-modulated the expression of TS and survivin and promoted sensitivity to 5-FU above and beyond the level achievable with Ca(2+) alone. Nifedipine by itself, however, had no effect on the suppression of TS or survivin or sensitivity to 5-FU. The action of Ca(2+) or in combination with nifedipine was entirely CaSR dependent as the aforementioned effects did not occur in CaSR knocked down cells. siRNAs targeting TS or survivin or both could mimic the effect of CaSR activation in promoting sensitivity to 5-FU. We conclude that nifedipine acts in synergy with Ca(2+) in activating CaSR and in promoting sensitivity to 5-FU by down modulating the expression of TS and survivin. G-protein coupled CaSR has the potential of serving as a target for improving therapeutic outcome in colon cancer.

摘要

我们之前曾报道过,细胞外钙离子激活 G 蛋白偶联钙敏感受体(CaSR)可下调胸苷酸合成酶(TS)和存活素的表达,并提高人结肠癌细胞对氟尿嘧啶的敏感性。在这里,我们首次报道了心脏药物硝苯地平与 Ca(2+)协同作用,激活 CaSR 并诱导细胞内 Ca(2+)增加。硝苯地平与 Ca(2+)联合使用可显著下调 TS 和存活素的表达,并提高对 5-FU 的敏感性,超过单独使用 Ca(2+)的效果。然而,硝苯地平本身对 TS 或存活素的抑制或对 5-FU 的敏感性没有影响。Ca(2+)或与硝苯地平联合作用完全依赖于 CaSR,因为上述作用不会在 CaSR 敲低细胞中发生。靶向 TS 或存活素或两者的 siRNA 可模拟 CaSR 激活对提高 5-FU 敏感性的作用。我们的结论是,硝苯地平与 Ca(2+)协同作用激活 CaSR,并通过下调 TS 和存活素的表达来促进对 5-FU 的敏感性。G 蛋白偶联 CaSR 有可能成为改善结肠癌治疗效果的靶点。

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