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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蛋白水平与前列腺肿瘤进展相关并诱导癌细胞依赖CXCR4的迁移

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摘要

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:我们较早地发现子宫内膜癌中线粒体核糖体蛋白S18-2(MRPS18-2,S18-2)的异常表达与增生和正常子宫内膜的表达相比。在这里,我们报道在前列腺癌(PCa)的临床标本中,S18-2的表达随疾病进展而增加。上皮细胞向间质细胞转化(EMT)的诱导水平与PCa细胞系中S18-2的表达水平相关。此外,如在斑马鱼胚胎模型和跨孔测定中所评估的,细胞在S18-2过表达时获得了提高的迁移能力。我们发现这是由于CXCR4细胞表面表达增加所致。中和CXCR4蛋白或废除细胞中的S18-2表达会大大降低其针对CXCL12的迁移能力。 TWIST2的mRNA表达,编码在CXCR4增加时诱导EMT的转录因子之一,与S18-2蛋白水平正相关。总之,这些数据表明,S18-2蛋白通过TWIST2 / E-钙粘着蛋白信号传导诱导EMT,并因此通过CXCR4介导的PCa细胞迁移。

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