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首页> 外文期刊>BMB Reports >Glucose regulated protein 78 promotes cell invasion via regulation of uPA production and secretion in colon cancer cells
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Glucose regulated protein 78 promotes cell invasion via regulation of uPA production and secretion in colon cancer cells

机译:葡萄糖调节蛋白78通过调节UPA生产和分泌在结肠癌细胞中促进细胞侵袭

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Glucose regulated protein 78 (GRP78) is frequently highly expressed in tumor cells, contributing to the acquisition of several phenotypic cancer hallmarks. GRP78 expression is also positively correlated with tumor metastasis, and promotes hepatocellular carcinoma cell invasion via increasing cell motility, however, other mechanisms involving the prometastatic roles of GRP78 remain to be elucidated. Here we report that forced GRP78 expression promotes colon cancer cell migration and invasion through upregulating MMP-2, MMP-9 and especially uPA production. These effects of GRP78 are mediated by enhancing the activation of β-catenin signaling. Interestingly, we identify that GRP78 interacts with uPA both in the cells and in the culture medium, suggesting that GRP78 protein is likely to directly facilitate uPA secretion via protein-protein interaction. Taken together, our findings demonstrate for the first time that besides stimulation of cell motility, GRP78 can act by increasing proteases production to promote tumor cell invasion.
机译:葡萄糖调节蛋白质78(GRP78)经常在肿瘤细胞中高度表达,有助于收购几种表型癌症标志。 GRP78表达也与肿瘤转移呈正相关,通过增加细胞活力促进肝细胞癌细胞侵袭,然而,涉及GRP78的常规作用的其他机制仍然阐明。在这里,我们通过上调MMP-2,MMP-9和尤其是UPA生产来报告强制GRP78表达促进结肠癌细胞迁移和侵袭。通过增强β-catenin信号传导的激活来介导的GRP78的这些效果。有趣的是,鉴定GRP78在细胞和培养基中均在UPA中与UPA相互作用,表明GRP78蛋白可能直接通过蛋白质 - 蛋白质相互作用促进UPA分泌。在一起,我们的研究结果首次证明了除了刺激细胞运动之外,GRP78可以通过增加蛋白酶产生来促进肿瘤细胞侵袭。

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