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格列本脲通过抑制卵巢透明细胞癌细胞 ES-2 中血小板衍生生长因子的分泌来抑制细胞侵袭。

Suppression of cellular invasion by glybenclamide through inhibited secretion of platelet-derived growth factor in ovarian clear cell carcinoma ES-2 cells.

机构信息

Department of Applied Chemistry, Faculty of Science and Technology, Keio University, Yokohama, Japan.

出版信息

FEBS Lett. 2012 May 21;586(10):1504-9. doi: 10.1016/j.febslet.2012.04.007. Epub 2012 Apr 25.

DOI:10.1016/j.febslet.2012.04.007
PMID:22673517
Abstract

It has been demonstrated that potassium channels (K(+) channels) play significant roles in some malignant phenotypes. Here, we provide the first evidence that treatment with glybenclamide, an ATP-sensitive K(+) channel blocker, inhibited cell migration in an ovarian clear cell carcinoma cell line, ES-2. Treatment with glybenclamide or knockdown by siRNA targeted against K(+) channel subunits demonstrated the suppression of ovarian cancer cell invasion, which occurred via inhibition of PDGF-AA secretion. Therefore, our findings suggest that K(+) channel blockers may be useful chemotherapeutic drugs for blocking the invasiveness of ovarian cancers.

摘要

已有研究表明,钾通道(K(+) 通道)在某些恶性表型中发挥着重要作用。在这里,我们首次提供证据表明,ATP 敏感性 K(+) 通道阻滞剂格列本脲治疗可抑制卵巢透明细胞癌细胞系 ES-2 中的细胞迁移。用格列本脲处理或用针对 K(+) 通道亚基的 siRNA 敲低,可抑制卵巢癌细胞侵袭,这是通过抑制 PDGF-AA 分泌来实现的。因此,我们的研究结果表明,K(+) 通道阻滞剂可能是用于阻断卵巢癌侵袭性的有用化疗药物。

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