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M-Phase Phosphoprotein 9 upregulation associates with poor prognosis and activates mTOR signaling in gastric cancer

机译:M相磷蛋白9预后差和激活胃癌中的MTOR信号传导的伴随助理

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The function of M-Phase Phosphoprotein 9 (MPHOSPH9) has not been investigated in gastric cancer yet. In the present study, the public cancer databases Oncomine and TCGA were analyzed, and MPHOSPH9 was found upregulated in gastric cancer tumor tissues. Immunohistochemistry (IHC) was also carried out to further confirm the results, and IHC analysis showed MPHOSPH9 was elevated in tumor tissues compared with the paracancerous tissues. QRT-PCR analysis also revealed that MPHOSPH9 mRNA was upregulated in gastric cancer cell lines. In addition, Kaplan–Meier estimates showed gastric cancer patients with high MPHOSPH9 level predicted a poor prognosis. Then, Western blot and CCK-8 assay showed overexpressed MPHOSPH9 enhanced gastric cancer cell proliferation, but MPHOSPH9 knockdown suppressed gastric cancer cell proliferation. Additionally, Western blot showed that MPHOSPH9 regulated the activation of mTOR, and overexpressed MPHOSPH9 reduced the inhibitory effects of mTOR inhibitors on cell survival in gastric cancer cells. Taken together, our results suggested that MPHOSPH9 .could be an oncogene in gastric cancer by regulating mTOR signaling.
机译:尚未在胃癌中研究M相磷蛋白9(MPhosph9)的功能。在本研究中,分析了公共癌症数据库oncommase和TCGA,发现胃癌肿瘤组织中的MPHOSH7上调。还进行了免疫组织化学(IHC)以进一步证实结果,与副血管组织相比,IHC分析显示在肿瘤组织中升高了MPHOSP9。 QRT-PCR分析还揭示了MPHOSH7 mRNA在胃癌细胞系中上调。此外,Kaplan-Meier估计显示胃癌患者高棉米磷患者预测预后差。然后,Western印迹和CCK-8测定显示过表达的MPHOSH7增强的胃癌细胞增殖,但MPHOSH77敲低抑制胃癌细胞增殖。另外,Western印迹表明,MPHOSH7调节了MTOR的活化,过表达的MPHOMP9降低了MTOR抑制剂对胃癌细胞中细胞存活的抑制作用。我们的结果表明,通过调节MTOR信号传导,MPHOSP7。可以是胃癌中的癌基因。

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