MicroRNA-592 targets IGF-1R to suppress cellular proliferation, migration and invasion in hepatocellular carcinoma

被引:23
作者
Wang, Wenyao [1 ]
Zhang, Hongfei [1 ]
Tang, Mao [1 ]
Liu, Longlong [1 ]
Zhou, Zhengfang [1 ]
Zhang, Shaojun [1 ]
Wang, Lichao [1 ]
机构
[1] Hebei Med Univ, Hosp 2, Dept Gen Surg, 80 Huanghe Rd, Shijiazhuang 050000, Hebei, Peoples R China
关键词
FACTOR; 1; RECEPTOR; TUMOR PROGRESSION; GROWTH; METASTASIS; MIR-592; EXPRESSION; RESISTANCE; PROGNOSIS; CELLS; LUNG;
D O I
10.3892/ol.2017.5902
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
NlicroRNAs (miRs) can function as tumor suppressors or oncogenes in different types of human malignancy, and may provide an effective therapy for cancer. The expression and functions of miR-592 have previously been studied in relation to cancer. However, the expression and potential functions of miR-592 in hepatocellular carcinoma (HCC) are still unknown. Using quantitative polymerasc chain reaction, MITT assays, cellular migration and invasion assays, bioinformatics software, western blot analysis and dual-luciferase report assays, the present study explored the expression and roles of miR-592 in HCC. it was identified that miR-592 was significantly downregulated in HCC tissues and cell lines. The statistical analysis revealed that low expression of miR-592 was evidently associated with tumor node metastasis stage and lymph node metastasis. Additionally, the present study provided the first evidence that miR-592 was likely to directly target the insulin-like growth factor 1 receptor in vitro. The present results indicated that miR-592 could be investigated as an efficacious therapeutic target for HCC in the future.
引用
收藏
页码:3522 / 3528
页数:7
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