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Lentivirus-Mediated Overexpression of MicroRNA-199a Inhibits Cell Proliferation of Human Hepatocellular Carcinoma
被引:80
|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.
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页码:237 / 244
页数:8
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