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首页> 外文期刊>American Journal of Translational Research >m6A demethylase FTO promotes hepatocellular carcinoma tumorigenesis via mediating PKM2 demethylation
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m6A demethylase FTO promotes hepatocellular carcinoma tumorigenesis via mediating PKM2 demethylation

机译:M6A脱甲基酶FTO通过介导PKM2去甲基化促进肝细胞癌肿瘤内血

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摘要

N6-methyladenosine (m6A) acts as the most common mRNA modification in mammal cells. Fat Mass and Obesity-associated protein (FTO) is the firstly identified demethylase in the m6A modification. This research tries to discover the potential roles of FTO in the m6A modification in the hepatocellular carcinoma (HCC). FTO level was found to be up-regulated in the HCC tissue and cells. The over-expression of FTO was correlated to the poor prognosis of HCC individuals. Knockdown of FTO suppressed the proliferation and in vivo tumor growth, and induced the G0/G1 phase arrest. Mechanically, FTO triggered the demethylation of PKM2 mRNA and accelerated the translated production. Overall, this finding suggests the critical function of FTO in the HCC oncogenesis and its m6A modification.
机译:N6-甲基腺苷(M6A)是哺乳动物细胞中最常见的mRNA改性。 脂肪质量和肥胖相关的蛋白质(FTO)是M6A改性中的第一个鉴定的去甲基化酶。 该研究试图发现FTO在肝细胞癌(HCC)中M6A改性中的潜在作用。 发现FTO水平在HCC组织和细胞中上调。 FTO的过表达与HCC个人的不良预后相关。 FTO的敲低抑制了增殖和体内肿瘤生长,并诱导G0 / G1相阻滞。 机械地,FTO引发了PKM2 mRNA的去甲基化,加速了翻译的生产。 总体而言,该发现表明FTO在HCC脑发生中的临界功能及其M6A修改。

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