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微小RNA-195通过靶向成纤维细胞生长因子2(FGF2)和血管内皮生长因子A(VEGFA),成为肝细胞癌转移的关键负调控因子。

MiR-195 is a key negative regulator of hepatocellular carcinoma metastasis by targeting FGF2 and VEGFA.

作者信息

Wang Min, Zhang Junjie, Tong Linlong, Ma Xiaofei, Qiu Xinguang

机构信息

Department of General Surgery, The First Affiliated Hospital of Zhengzhou UniversityZhengzhou 450052, China; Department of General Surgery, People's Hospital of ZhengzhouZhengzhou 450003, China.

Department of General Surgery, People's Hospital of Zhengzhou Zhengzhou 450003, China.

出版信息

Int J Clin Exp Pathol. 2015 Nov 1;8(11):14110-20. eCollection 2015.

Abstract

Hepatocellular carcinoma (HCC) is the most common primary tumor of liver and the fifth most common cancer in the world. Lung is the most frequent site for extra hepatic metastasis from hepatocellular carcinoma, while the cause and mechanism of it is still poor understood. Here, we identify that the expression of miR-195 is markedly impaired in the lung metastasis cell lines of HCC. The result of Real-time PCR reveals the expression of miR-195 is significantly downregulated in 92 HCC tissues. Low expression of miR-195 is associated with tumor size, portal vein thrombosis, TNM stage and patients survival. Luciferase reporter and ELISA assay prove that hematogenous metastasis related genes including FGF2 and VEGFA are the target genes of miR-195. Overexpression of miR-195 in HCC cell line BEL-7402 markedly inhibits the capability of migration and invasion. Taken together, our results suggest that miR-195, a tumor suppressor miRNA, contributes to the lung metastasis of HCC by negatively regulating FGF2 and VEGFA, providing key implications of miR-195 for the therapeutic intervention of HCC.

摘要

肝细胞癌(HCC)是肝脏最常见的原发性肿瘤,也是全球第五大常见癌症。肺是肝细胞癌肝外转移最常见的部位,但其发生原因和机制仍不清楚。在此,我们发现miR-195在肝癌肺转移细胞系中的表达明显受损。实时荧光定量PCR结果显示,92例肝癌组织中miR-195的表达显著下调。miR-195低表达与肿瘤大小、门静脉血栓形成、TNM分期及患者生存相关。荧光素酶报告基因和ELISA分析证明,包括FGF2和VEGFA在内的血行转移相关基因是miR-195的靶基因。在肝癌细胞系BEL-7402中过表达miR-195可显著抑制其迁移和侵袭能力。综上所述,我们的结果表明,肿瘤抑制性miRNA miR-195通过负调控FGF2和VEGFA促进肝癌的肺转移,为肝癌的治疗干预提供了关于miR-195的关键启示。

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