首页> 外文期刊>Gut: Journal of the British Society of Gastroenterology >The putative tumour suppressor microRNA-124 modulates hepatocellular carcinoma cell aggressiveness by repressing ROCK2 and EZH2.
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The putative tumour suppressor microRNA-124 modulates hepatocellular carcinoma cell aggressiveness by repressing ROCK2 and EZH2.

机译:推定的抑癌基因microRNA-124通过抑制ROCK2和EZH2来调节肝癌细胞的侵袭性。

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BACKGROUND: Recent profile studies of microRNA (miRNA) expression have documented a deregulation of miRNA (miR-124) in hepatocellular carcinoma (HCC). OBJECTIVE: To determine the status of miR-124 expression and its underlying mechanisms in the pathogenesis of HCC. METHODS: The expression levels of miR-124 were first examined in HCC cell lines and tumour tissues by real-time PCR. The in vitro and in vivo functional effect of miR-124 was examined further. A luciferase reporter assay was conducted to confirm target associations. RESULTS: The expression levels of miR-124 were frequently reduced in HCC cells and tissues, and low-level expression of miR-124 was significantly associated with a more aggressive and/or poor prognostic phenotype of patients with HCC (p<0.05). In HCC cell lines, stable overexpression of miR-124 was sufficient to inhibit cell motility and invasion in vitro, and suppress intrahepatic and pulmonary metastasis in vivo. In addition, ectopic overexpression of miR-124 in HCC cells inhibited epithelial-mesenchymal cell transition, formation of stress fibres, filopodia and lamellipodia. Further studies showed that miR-124 could directly target the 3'-untranslated region (3'-UTR) of both ROCK2 and EZH2 mRNAs, and suppress their mRNA and protein expressions. These findings suggest that miR-124 plays a critical role in regulating cytoskeletal events and epithelial-mesenchymal cell transition and, ultimately, inhibits the invasive and/or metastatic potential of HCC, probably by its direct target on ROCK2 and EZH2 genes. These results provide functional and mechanistic links between the tumour suppressor miRNA-124 and the two oncogenes ROCK2 and EZH2 on the aggressive nature of HCC. CONCLUSION: These data highlight an important role for miR-124 in the regulation of invasion and metastasis in the molecular aetiology of HCC, and suggest a potential application of miR-124 in prognosis prediction and cancer treatment.
机译:背景:最近对microRNA(miRNA)表达的研究表明,肝细胞癌(HCC)中miRNA(miR-124)的失控。目的:确定miR-124表达的状态及其在肝癌发病机理中的作用机制。方法:首先通过实时荧光定量PCR检测miR-124在肝癌细胞株和肿瘤组织中的表达水平。进一步检查了miR-124的体外和体内功能作用。进行荧光素酶报告基因测定以确认靶标关联。结果:miR-124在肝细胞癌组织和组织中的表达水平经常降低,而miR-124的低水平表达与HCC患者的侵袭性和/或不良预后表型显着相关(p <0.05)。在HCC细胞系中,miR-124的稳定过度表达足以抑制体外细胞运动和侵袭,并在体内抑制肝内和肺转移。此外,HCC细胞中miR-124的异位过表达抑制了上皮-间充质细胞的转化,应激纤维的形成,丝状伪足和片状脂质体。进一步的研究表明,miR-124可以直接靶向ROCK2和EZH2 mRNA的3'-非翻译区(3'-UTR),并抑制其mRNA和蛋白表达。这些发现表明,miR-124在调节细胞骨架事件和上皮-间充质细胞转化中起着至关重要的作用,并且最终可能通过直接靶向ROCK2和EZH2基因来抑制HCC的侵袭和/或转移潜能。这些结果提供了在肿瘤抑制因子miRNA-124与两种癌基因ROCK2和EZH2之间对肝癌的侵袭性的功能和机理联系。结论:这些数据突出了miR-124在肝癌分子病因学中调控侵袭和转移的重要作用,并暗示了miR-124在预后预测和癌症治疗中的潜在应用。

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