Lentivirus-Mediated Overexpression of MicroRNA-199a Inhibits Cell Proliferation of Human Hepatocellular Carcinoma

被引:81
作者
Jia, Xiao Qin [2 ,3 ,4 ]
Cheng, Hai Qing [1 ,2 ,3 ]
Qian, Xu [2 ,3 ]
Bian, Chuan Xiu [2 ,3 ]
Shi, Zhu Mei [2 ,3 ]
Zhang, Jian Ping [5 ]
Jiang, Bing Hua [2 ,3 ]
Feng, Zhen Qing [1 ,2 ,3 ]
机构
[1] Nanjing Med Univ, Minist Hlth, Key Lab Antibody Tech, Nanjing 210029, Peoples R China
[2] Nanjing Med Univ, Ctr Canc, Nanjing 210029, Peoples R China
[3] Nanjing Med Univ, Dept Pathol, Nanjing 210029, Peoples R China
[4] Yangzhou Univ, Dept Pathol, Yangzhou 225001, Peoples R China
[5] Nanjing Med Univ, Affiliated Hosp 2, Dept Gen Surg, Nanjing 210011, Peoples R China
关键词
miR-199a; Hepatocellular carcinoma; Cell proliferation; Hypoxia inducible factor-1 alpha; HepG2; HYPOXIA; SIGNATURES; BIOLOGY; GROWTH;
D O I
10.1007/s12013-011-9263-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
microRNA-199a (miR-199a) is a highly conserved miRNA, always deregulated in numerous human tumors. The results of microarray analysis indicated that miR-199a was frequently downregulated in hepatocellular carcinoma (HCC). The expression levels of miR-199a in 11 pairs of matched HCC neoplastic and adjacent non-neoplastic tissues, 5 HCC cell lines and liver cell line L02 were examined by quantitative real-time PCR analysis. We found miR-199a was significantly down-regulated in HCC tissues when compared with pair-matched adjacent non-tumor tissues. We also found the expression level of miR-199a was also substantially decreased in several human HCC cell lines including SMMC-7721, BEL-7402, BEL-7701, MHCC97H, and HepG2. To investigate the role of miR-199a in tumorigenesis, we developed a lentiviral vector for the expression of pre-miR-199a (Lenti-miR-199a). Lenti-miR-199a inhibited HCC cell proliferation in vitro and in vivo. Compared to parental cells or cells transfected with a control vector, the overexpression of microRNA-199a in the HCC cell lines HepG2 stably was showed to reduce cell proliferation in vitro and in vivo. Luciferase reporter assay revealed the regulation of miR-199a on 3'-UTR of HIF-1 alpha. Further investigation confirmed that miR-199a significantly reduced the endogenous protein level of HIF-1 alpha in hypoxia. MiR-199a inhibits cell proliferation in vitro and in vivo partly through down-regulation of HIF-1 alpha in human HCC. Thus, these studies provide an important new insight into the pathogenesis of human HCC and it may open a new perspective for the development of effective gene therapy for human HCC.
引用
收藏
页码:237 / 244
页数:8
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