The putative tumour suppressor microRNA-124 modulates hepatocellular carcinoma cell aggressiveness by repressing ROCK2 and EZH2

小RNA 肝细胞癌 抑制器 岩石2 EZH2型 癌症研究 生物 医学 表观遗传学 细胞生物学 癌症 激酶 基因 遗传学 Rho相关蛋白激酶
作者
Fang Zheng,Yiji Liao,Mu-Yan Cai,Yan Hui Liu,Tian-Hao Liu,Shu-Peng Chen,Xiu‐Wu Bian,Xin‐Yuan Guan,Marie C. Lin,Yi-Xin Zeng,Hsiang‐Fu Kung,Dan Xie
出处
期刊:Gut [BMJ]
卷期号:61 (2): 278-289 被引量:376
标识
DOI:10.1136/gut.2011.239145
摘要

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.
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