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The MRPS18-2 protein levels correlate with prostate tumor progression and it induces CXCR4-dependent migration of cancer cells

机译:MRPS18-2蛋白质水平与前列腺肿瘤进展相关,并诱导CXCR4依赖性癌细胞的迁移

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We have earlier found abnormal expression of the mitochondrial ribosomal protein S18-2 (MRPS18-2, S18-2) in endometrial cancer, compared to the expression in hyperplasia and in normal endometrium. Here we report that expression of S18-2 was increased with disease progression in clinical specimens of prostate cancer (PCa). The level of induction of epithelial to mesenchymal cell transition (EMT) correlated with the expression level of S18-2 in PCa cell lines. Moreover, cells acquired increased ability of migration upon S18-2 overexpression, as was evaluated in zebrafish embryo model and in trans-well assay. We found that this is due to increased CXCR4 cell surface expression. Neutralizing CXCR4 protein or abrogating S18-2 expression in cells significantly reduced their migratory ability directed toward CXCL12. The mRNA expression of TWIST2, encoding one of transcription factors that induce EMT upon CXCR4 increase, positively correlated with the S18-2 protein level. Together, these data suggest that the S18-2 protein induces EMT through the TWIST2/E-cadherin signalling and, consequently, CXCR4-mediated migration of PCa cells.
机译:与增生和正常子宫内膜中的表达相比,我们早先发现子宫内膜核糖体蛋白S18-2(MRPS18-2,S18-2)中的线粒体核糖体蛋白S18-2(MRPS18-2,S18-2)的异常表达。在这里,我们认为S18-2的表达随着前列腺癌(PCA)的临床标本中的疾病进展而增加。上皮对间充质细胞转变(EMT)的诱导水平与PCA细胞系中S18-2的表达水平相关。此外,细胞在S18-2过表达上获得了迁移能力,如斑马鱼胚胎模型和反式井测定中的评价。我们发现这是由于CXCR4细胞表面表达增加。中和CXCR4蛋白或消除细胞中的S18-2表达显着降低了针对CXCL12的迁移能力。 Twist2的mRNA表达,编码在CXCR4上诱导EMT的转录因子之一增加,与S18-2蛋白质水平正相关。这些数据表明,S18-2蛋白通过Twist2 / E-钙粘蛋白信号传导诱导EMT,并且因此CXCR4介导的PCA细胞迁移。

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