The function of miRNAs in hepatocarcinogenesis induced by hepatitis B virus X protein

被引:19
作者
Wang, Ziyao [1 ]
Wu, Zhongjun [1 ]
Huang, Ping [1 ]
机构
[1] Chongqing Med Univ, Affiliated Hosp 1, Dept Hepatobiliary Surg, Natl Key Clin Dept, Youyi Rd 1, Chongqing 400000, Peoples R China
关键词
MicroRNA; HBx; hepatocarcinogenesis; interaction; mechanism; HEPATOCELLULAR-CARCINOMA CELLS; ABNORMAL LIPID-METABOLISM; ABERRANT DNA METHYLATION; NF-KAPPA-B; DOWN-REGULATION; UP-REGULATION; LIVER-CANCER; HEPATOMA-CELLS; PROMOTES PROLIFERATION; EPIGENETIC REPRESSION;
D O I
10.3892/or.2017.5716
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs are short RNAs that play a crucial role in all biological processes through post-transcriptional regulation for protein-coding genes and inducing mRNA degradation. Hepatitis B virus infection has been considered as a major risk factor in hepatocellular carcinoma, further research indicates that hepatitis B virus X protein (HBx) is one of the critical links of hepatocarcinogenesis. HBx takes part in hepatocarcinogenesis via regulating transcription, signal transduction, apoptosis, protein degradation and DNA repair. miRNA is the important target gene of HBx, their interaction impacts many tumor processes, such as proliferation, apoptosis, invasion, metastasis, differentiation and adipogenesis. In the present study we reviewed the current state of knowledge of regulation pathway of HBx acting on miRNAs, and focused on the role of their interplay in hepatocarcinogenesis.
引用
收藏
页码:652 / 664
页数:13
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[31]   Hepatitis B virus-induced hepatocarcinogenesis: A virological and oncological perspective [J].
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[32]   Interleukin-32 expression induced by hepatitis B virus protein X is mediated through activation of NF-κB [J].
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[33]   SIRT1 sensitizes hepatocellular carcinoma cells expressing hepatitis B virus X protein to oxidative stress-induced apoptosis [J].
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[34]   C-terminal-truncated hepatitis B virus X protein promotes hepatocarcinogenesis by activating the MAPK pathway [J].
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[36]   Proteomic Profiling Identifies Aberrant Epigenetic Modifications Induced by Hepatitis B Virus X Protein [J].
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[37]   Modulation of Apoptotic Signaling by the Hepatitis B Virus X Protein [J].
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[38]   Epigenetic control of metastasis-associated protein 1 gene expression by hepatitis B virus X protein during hepatocarcinogenesis [J].
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Seong, J-K ;
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[39]   Hepatitis B virus HBx gene and hepatocarcinogenesis [J].
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