Non-coding RNA Associated Competitive Endogenous RNA Regulatory Network: Novel Therapeutic Approach in Liver Fibrosis

被引:30
作者
Riaz, Farooq [1 ,2 ]
Li, Dongmin [1 ,2 ]
机构
[1] Xi An Jiao Tong Univ, Hlth Sci Ctr, Sch Basic Med Sci, Dept Biochem & Mol Biol, Xian 710061, Shaanxi, Peoples R China
[2] Minist Educ, Key Lab Environm & Genes Related Dis, Xian 710061, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Liver fibrosis; non-coding RNA; competing endogenous RNA; NAFLD; circular RNA; microRNA; HEPATIC STELLATE CELLS; CIRCULAR RNAS; TRANSCRIPTIONAL ACTIVITY; MICRORNA EXPRESSION; ALTERED EXPRESSION; GENE-EXPRESSION; REVEALS; MECHANISMS; FIBROGENESIS; PROGRESSION;
D O I
10.2174/1566523219666191107113046
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Liver fibrosis or scarring is the most common pathological feature caused by chronic liver injury, and is widely considered one of the primary causes of morbidity and mortality. It is primarily characterised by hepatic stellate cells (HSC) activation and excessive extracellular matrix (ECM) protein deposition. Overwhelming evidence suggests that the dysregulation of several noncoding RNAs (lncRNAs), mainly long non-coding RNAs (lncRNAs), microRNAs (miRNAs) and circular RNAs (circRNAs) contributes to the activation of HSC and progression of liver fibrosis. These ncRNAs not only bind to their target genes for the development and regression of liver fibrosis but also act as competing endogenous RNAs (ceRNAs) by sponging with miRNAs to form signaling cascades. Among these signaling cascades, lncRNA-miRNA-mRNA and circRNA-miRNA-mRNA are critical modulators for the initiation, progression, and regression of liver fibrosis. Thus, targeting these interacting ncRNA cascades can serve as a novel and potential therapeutic target for inhibition of HSC activation and prevention and regression of liver fibrosis.
引用
收藏
页码:305 / 317
页数:13
相关论文
共 115 条
[1]   Circular RNAs as Promising Biomarkers: A Mini-Review [J].
Abu, Nadiah ;
Jamal, Rahman .
FRONTIERS IN PHYSIOLOGY, 2016, 7
[2]   MicroRNA functions in animal development and human disease [J].
Alvarez-Garcia, I ;
Miska, EA .
DEVELOPMENT, 2005, 132 (21) :4653-4662
[3]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[4]   MORPHOLOGY OF CIRRHOSIS [J].
ANTHONY, PP ;
ISHAK, KG ;
NAYAK, NC ;
POULSEN, HE ;
SCHEUER, PJ ;
SOBIN, LH .
JOURNAL OF CLINICAL PATHOLOGY, 1978, 31 (05) :395-414
[5]   A Liver-Specific Long Noncoding RNA With a Role in Cell Viability Is Elevated in Human Nonalcoholic Steatohepatitis [J].
Atanasovska, Biljana ;
Rensen, Sander S. ;
van der Sijde, Marijke R. ;
Marsman, Glenn ;
Kumar, Vinod ;
Jonkers, Iris ;
Withoff, Sebo ;
Shiri-Sverdlov, Ronit ;
Greve, Jan Willem M. ;
Faber, Klaas Nico ;
Moshage, Han ;
Wijmenga, Cisca ;
van de Sluis, Bart ;
Hofker, Marten H. ;
Fu, Jingyuan .
HEPATOLOGY, 2017, 66 (03) :794-808
[6]   miR-122-A key factor and therapeutic target in liver disease [J].
Bandiera, Simonetta ;
Pfeffer, Sebastien ;
Baumert, Thomas F. ;
Zeisel, Mirjam B. .
JOURNAL OF HEPATOLOGY, 2015, 62 (02) :448-457
[7]   New advances of lncRNAs in liver fibrosis, with specific focus on lncRNA-miRNA interactions [J].
Bian, Er-Bao ;
Xiong, Zhi-Gang ;
Li, Jun .
JOURNAL OF CELLULAR PHYSIOLOGY, 2019, 234 (03) :2194-2203
[8]   Hotair facilitates hepatic stellate cells activation and fibrogenesis in the liver [J].
Bian, Er-Bao ;
Wang, Yuan-Yuan ;
Yang, Yang ;
Wu, Bao-Ming ;
Xu, Tao ;
Meng, Xiao-Ming ;
Huang, Cheng ;
Zhang, Lei ;
Lv, Xiong-Wen ;
Xiong, Zhi-Gang ;
Li, Jun .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2017, 1863 (03) :674-686
[9]   Liver Immunology [J].
Bogdanos, Dimitrios P. ;
Gao, Bin ;
Gershwin, M. Eric .
COMPREHENSIVE PHYSIOLOGY, 2013, 3 (02) :567-598
[10]   RNA polymerase III transcribes human microRNAs [J].
Borchert, Glen M. ;
Lanier, William ;
Davidson, Beverly L. .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2006, 13 (12) :1097-1101