Regulatory Functions and Mechanisms of Circular RNAs in Hepatic Stellate Cell Activation and Liver Fibrosis

Author:

Nokkeaw Archittapon,Thamjamrassri Pannathon,Tangkijvanich PisitORCID,Ariyachet ChaiyabootORCID

Abstract

Chronic liver injury induces the activation of hepatic stellate cells (HSCs) into myofibroblasts, which produce excessive amounts of extracellular matrix (ECM), resulting in tissue fibrosis. If the injury persists, these fibrous scars could be permanent and disrupt liver architecture and function. Currently, effective anti-fibrotic therapies are lacking; hence, understanding molecular mechanisms that control HSC activation could hold a key to the development of new treatments. Recently, emerging studies have revealed roles of circular RNAs (circRNAs), a class of non-coding RNAs that was initially assumed to be the result of splicing errors, as new regulators in HSC activation. These circRNAs can modulate the activity of microRNAs (miRNAs) and their interacting protein partners involved in regulating fibrogenic signaling cascades. In this review, we will summarize the current knowledge of this class of non-coding RNAs for their molecular function in HSC activation and liver fibrosis progression.

Funder

Thailand Science research and Innovation Fund Chulalongkorn University

Ratchadapiseksompotch Fund, Faculty of Medicine, Chulalongkorn University

Thailand Research Fund (TRF) Senior Research Scholar

Center of Excellence in Hepatitis and Liver Cancer, Faculty of Medicine, Chulalongkorn University

Publisher

MDPI AG

Subject

General Medicine

Reference211 articles.

1. Liver fibrosis;Bataller;J. Clin. Investig.,2005

2. Hepatic stellate cells: Protean, multifunctional, and enigmatic cells of the liver;Friedman;Physiol. Rev.,2008

3. Pathogenesis of liver fibrosis;Friedman;Annu. Rev. Pathol.,2011

4. Liver fibrosis—From bench to bedside;Friedman;J. Hepatol.,2003

5. Cellular and molecular mechanisms in the pathogenesis of liver fibrosis: An update;Elpek;World J. Gastroenterol.,2014

Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3