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首页> 外文期刊>Molecular Nutrition and Food Research >Glabridin, an isoflavan from licorice root, inhibits migration, invasion and angiogenesis of MDA-MB-231 human breast adenocarcinoma cells by inhibiting focal adhesion kinase/Rho signaling pathway.
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Glabridin, an isoflavan from licorice root, inhibits migration, invasion and angiogenesis of MDA-MB-231 human breast adenocarcinoma cells by inhibiting focal adhesion kinase/Rho signaling pathway.

机译:Glabridin是甘草根中的异黄烷,通过抑制粘着斑激酶/ Rho信号通路来抑制MDA-MB-231人乳腺腺癌细胞的迁移,侵袭和血管生成。

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摘要

Scope: In this study we first report the antimigration, antiinvasive effect of glabridin, a flavonoid obtained from licorice, in MDA-MB-231 human breast adenocarcinoma cells. Methods and results: Glabridin exhibited effective inhibition of cell metastasis by decreasing cancer cell migration and invasion of MDA-MB-231 cells. In addition, glabridin also blocked human umbilical vein endothelial cells (HUVEC) migration and decreased MDA-MB-231-mediated angiogenesis. Further investigation revealed that the inhibition of cancer angiogenesis by glabridin was also evident in a nude mice model. Blockade of MDA-MB-231 cells and HUVEC migration was associated with an increase of alpha gamma beta3 integrin proteosome degradation. Glabridin also decreased the active forms of FAK and Src, and enhanced levels of inactivated phosphorylated Src (Tyr 416), decreasing the interaction of FAK and Src. Inhibition of the FAK/Src complex by glabridin also blocked AKT and ERK1/2 activation, resulting in reduced activation of RhoA as well as myosin light chain phosphorylation. Conclusion: This study demonstrates that glabridin may be a novel anticancer agent for the treatment of breast cancer in three different ways: inhibition of migration, invasion and angiogenesis.
机译:范围:在这项研究中,我们首先报道了麦草精(一种从甘草中获得的类黄酮)在MDA-MB-231人乳腺癌细胞中的抗迁移,抗侵袭作用。方法和结果:通过降低癌细胞的迁移和MDA-MB-231细胞的侵袭,格拉布里丁对细胞转移具有有效的抑制作用。此外,加拉普丁还阻断了人脐静脉内皮细胞(HUVEC)的迁移并减少了MDA-MB-231介导的血管生成。进一步的研究表明,在裸鼠模型中,加拉普丁对癌症血管生成的抑制作用也很明显。 MDA-MB-231细胞的封锁和HUVEC迁移与αγbeta3整合素蛋白体降解的增加有关。 Glabridin还降低了FAK和Src的活性形式,并增强了失活的磷酸化Src(Tyr 416)的水平,从而降低了FAK和Src的相互作用。用麦角蛋白抑制FAK / Src复合物也阻断了AKT和ERK1 / 2的活化,导致RhoA的活化减少以及肌球蛋白轻链的磷酸化。结论:这项研究表明,加拉必定可能是一种通过三种不同方式治疗乳腺癌的新型抗癌药:抑制迁移,侵袭和血管生成。

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