
Aim. To investigate the expression of miR-940 in the hepatocellular carcinoma (HCC) and its impact on function and biological mechanism in the HCC cells.Methods. Quantitative RT-PCR analysis was used to quantify miR-940 expression in 46 cases of tissues and cells. Transfection of HCC cell lines was performed by miR-940 mimics; the abilities of invasion and migration were assessed through Transwell array. Western blot represents the alteration in expression of CXCR2 by miR-940 mimics.Results. miR-940 expression was decreased significantly in the HCC tissues and the relevant cell lines. miR-940 upregulation suppressed the invasion and migration of HCC cells in vitro. Furthermore, the CXCR2 was downregulated to suppress invasion and migration after miR-940 mimics. Moreover, decreased miR-940 expression was negatively correlated with Edmondson grade (P=0.008), tumor microsatellite or multiple tumors (P=0.04), vascular invasion (P=0.035), and recurrence and metastasis (P=0.038). Kaplan-Meier analysis demonstrated that decreased miR-940 expression contributed to poor overall survival (P<0.05).Conclusions. Our findings present that miR-940 acts as a pivotal adaptor of CXCR2 and its transcription downregulated CXCR2 expression to decrease HCC invasion and migration in vitro. Our study suggests that miR-940 may be a novel poor prognostic biomarker for HCC.
Male, Carcinoma, Hepatocellular, Liver Neoplasms, Receptors, Interleukin-8B, Neoplasm Proteins, Gene Expression Regulation, Neoplastic, MicroRNAs, Cell Movement, Cell Line, Tumor, Biomarkers, Tumor, Humans, Female, Neoplasm Invasiveness, RNA, Neoplasm, Research Article
Male, Carcinoma, Hepatocellular, Liver Neoplasms, Receptors, Interleukin-8B, Neoplasm Proteins, Gene Expression Regulation, Neoplastic, MicroRNAs, Cell Movement, Cell Line, Tumor, Biomarkers, Tumor, Humans, Female, Neoplasm Invasiveness, RNA, Neoplasm, Research Article
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