MiR-182 is up-regulated and targeting Cebpa in hepatocellular carcinoma

被引:46
|
作者
Wang, Chenggang [1 ,2 ]
Ren, Ren [3 ,4 ]
Hu, Haolin [3 ,4 ]
Tan, Changjun [5 ]
Han, Miao [3 ,4 ]
Wang, Xiaolin [1 ,2 ]
Zheng, Yun [6 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Intervent Radiol, Shanghai 200032, Peoples R China
[2] Shanghai Inst Med Imaging, Shanghai 200032, Peoples R China
[3] Fudan Univ, Sch Life Sci, State Key Lab Genet Engn, Shanghai 200433, Peoples R China
[4] Fudan Univ, Sch Life Sci, Inst Dev Biol & Mol Med, Shanghai 200433, Peoples R China
[5] Fudan Univ, Liver Canc Inst, Shanghai 200032, Peoples R China
[6] Kunming Univ Sci & Technol, Fac Life Sci & Technol, Kunming 650500, Peoples R China
关键词
miR-182; Cebpa; miR-122; hepatocellular carcinoma (HCC); oncogene; DOWN-REGULATION; STEM-CELLS; HUMAN MICRORNA; C/EBP-ALPHA; EXPRESSION; GENE; DIFFERENTIATION; DATABASE; TOOL; G1;
D O I
10.3978/j.issn.1000-9604.2014.01.01
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) are endogenous small non-coding RNAs that repress their targets at post transcriptional level. Existing studies have shown that miRNAs are important regulatory genes in hepatocellular carcinoma (HCC), as either tumor suppressors or oncogenes. MiR-122 is normally downregulated in HCC and regarded as a tumor suppressor. Recently miR-122 has been reported to be regulated by CEBPA, which is then involved in a novel pathway to influence proliferation of tumor cells. However it is unknown whether CEBPA is regulated by miRNAs in HCC. In this study, we find that miR-182 is upregulated in HCC model rat, and represses CEBPA in both rat and human. This further improves the current CEBPA/miR-122 pathway that controls the proliferation of tumor cells. These results suggest that miR-182 is a potential oncogene in HCC and could be used as a diagnostic marker and drug target of HCC.
引用
收藏
页码:17 / 29
页数:13
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