The potential of microRNAs in liver fibrosis

被引:106
作者
He, Yong [1 ]
Huang, Cheng [1 ]
Zhang, Sheng-peng [1 ]
Sun, Xu [1 ]
Long, Xiao-ran [1 ]
Li, Jun [1 ]
机构
[1] Anhui Med Univ, Anhui Key Lab Bioact Natrual Prod, Sch Pharm, Hefei 230032, Anhui, Peoples R China
关键词
miRNA; Liver fibrosis; Hepatic stellate cells; Signal transduction pathways; HEPATIC STELLATE CELL; TGF-BETA; RHEUMATOID-ARTHRITIS; DOWN-REGULATION; PDGF-B; ACTIVATION; EXPRESSION; MECHANISMS; APOPTOSIS; OVEREXPRESSION;
D O I
10.1016/j.cellsig.2012.07.023
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
MicroRNAs (miRNAs) are a class of similar to 22-nucleotides noncoding RNAs that regulate gene expression by specifically binding with 3'-untranslated region (3'-UTR) of target gene mRNAs to posttranscriptionally effect mRNA stability and translation,and play essential roles in a variety of biological processes, including cell development, proliferation, differentiation, and apoptosis. Liver fibrosis is the occurrence of liver cell necrosis and inflammatory stimulation, and is characterized by excessive accumulation of extracellular matrices(ECMs). In the fibrotic liver, hepatic stellate cells (HSCs), which are regulated by multiple signal transduction pathways, undergo myofibroblastic transdifferentiation and are generally regarded as the major ECM producer responsible for liver fibrosis. A growing body of evidence suggests that divergent miRNAs participate in liver fibrotic process and activation of HSC. Moreover, members of many signal transduction pathways are important targets for miRNAs. In this review, we make a summary on current understanding of the roles of miRNAs in the development of liver fibrosis, HSC functions and their potential as novel drug targets. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:2268 / 2272
页数:5
相关论文
共 53 条
[1]   Hepatic stellate cell: A star cell in the liver [J].
Atzori, Luigi ;
Poli, Giuseppe ;
Perra, Andrea .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2009, 41 (8-9) :1639-1642
[2]   MicroRNAs Regulating a Change of Heart [J].
Barringhaus, Kurt G. ;
Zamore, Phillip D. .
CIRCULATION, 2009, 119 (16) :2217-2224
[3]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[4]   TGFβ1 in liver fibrosis:: time to change paradigms? [J].
Bauer, M ;
Schuppan, D .
FEBS LETTERS, 2001, 502 (1-2) :1-3
[5]   Mechanisms and Biomarkers of Apoptosis in Liver Disease and Fibrosis [J].
Chakraborty, Jayashree Bagchi ;
Oakley, Fiona ;
Walsh, Meagan J. .
INTERNATIONAL JOURNAL OF HEPATOLOGY, 2012, 2012
[6]   Hepatic Stellate Cell-Specific Gene Silencing Induced by an Artificial MicroRNA for Antifibrosis In Vitro [J].
Chang, Ying ;
Jiang, Hua-jun ;
Sun, Xue-mei ;
Cai, Xiao-kun ;
He, Xing-xing ;
Li, Pei-yuan ;
Tang, Wang-xian ;
Song, Yu-hu ;
Lin, Ju-sheng .
DIGESTIVE DISEASES AND SCIENCES, 2010, 55 (03) :642-653
[7]   A polymorphism in the 3′-UTR of interleukin-1 receptor-associated kinase (IRAK1), a target gene of miR-146a, is associated with rheumatoid arthritis susceptibility [J].
Chatzikyriakidou, Anthoula ;
Voulgari, Paraskevi V. ;
Georgiou, Ioannis ;
Drosos, Alexandros A. .
JOINT BONE SPINE, 2010, 77 (05) :411-413
[8]   Loss of expression of miR-335 is implicated in hepatic stellate cell migration and activation [J].
Chen, Chao ;
Wu, Chao-Qun ;
Zhang, Zong-Qi ;
Yao, Ding-Kang ;
Zhu, Liang .
EXPERIMENTAL CELL RESEARCH, 2011, 317 (12) :1714-1725
[9]   Liver fibrosis induced by hepatic overexpression of PDGF-B in transgenic mice [J].
Czochra, Piotr ;
Klopcic, Borut ;
Meyer, Erik ;
Herkel, Johannes ;
Garcia-Lazaro, Jose Francisco ;
Thieringer, Florian ;
Schirmacher, Peter ;
Biesterfeld, Stefan ;
Galle, Peter R. ;
Lohse, Ansgar W. ;
Kanzler, Stephan .
JOURNAL OF HEPATOLOGY, 2006, 45 (03) :419-428
[10]  
Doh KO, 2008, KOREAN J PHYSIOL PHA, V12, P1, DOI 10.4196/kjpp.2008.12.1.1