Noncoding RNA-Mediated Epigenetic Regulation in Hepatic Stellate Cells of Liver Fibrosis.

IF 3.6 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ruoyu Gao, Jingwei Mao
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引用次数: 0

Abstract

Liver fibrosis is a significant contributor to liver-related disease mortality on a global scale. Despite this, there remains a dearth of effective therapeutic interventions capable of reversing this condition. Consequently, it is imperative that we gain a comprehensive understanding of the underlying mechanisms driving liver fibrosis. In this regard, the activation of hepatic stellate cells (HSCs) is recognized as a pivotal factor in the development and progression of liver fibrosis. The role of noncoding RNAs (ncRNAs) in epigenetic regulation of HSCs transdifferentiation into myofibroblasts has been established, providing new insights into gene expression changes during HSCs activation. NcRNAs play a crucial role in mediating the epigenetics of HSCs, serving as novel regulators in the pathogenesis of liver fibrosis. As research on epigenetics expands, the connection between ncRNAs involved in HSCs activation and epigenetic mechanisms becomes more evident. These changes in gene regulation have attracted considerable attention from researchers in the field. Furthermore, epigenetics has contributed valuable insights to drug discovery and the identification of therapeutic targets for individuals suffering from liver fibrosis and cirrhosis. As such, this review offers a thorough discussion on the role of ncRNAs in the HSCs activation of liver fibrosis.

非编码 RNA 介导的肝纤维化肝星状细胞表观遗传调控
在全球范围内,肝纤维化是造成肝脏相关疾病死亡的重要原因。尽管如此,能够逆转这种状况的有效治疗干预措施仍然匮乏。因此,我们必须全面了解驱动肝纤维化的潜在机制。在这方面,肝星状细胞(HSCs)的活化被认为是肝纤维化发生和发展的关键因素。非编码 RNA(ncRNA)在造血干细胞向肌成纤维细胞转分化的表观遗传调控中的作用已被证实,这为了解造血干细胞活化过程中基因表达的变化提供了新的视角。NcRNA 在介导造血干细胞表观遗传学方面发挥着关键作用,是肝纤维化发病机制中的新型调控因子。随着表观遗传学研究的深入,参与造血干细胞活化的 ncRNA 与表观遗传学机制之间的联系变得越来越明显。这些基因调控的变化引起了该领域研究人员的极大关注。此外,表观遗传学还为药物发现和确定肝纤维化和肝硬化患者的治疗靶点提供了宝贵的见解。因此,本综述深入探讨了 ncRNA 在造血干细胞激活肝纤维化过程中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Non-Coding RNA
Non-Coding RNA Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
6.70
自引率
4.70%
发文量
74
审稿时长
10 weeks
期刊介绍: Functional studies dealing with identification, structure-function relationships or biological activity of: small regulatory RNAs (miRNAs, siRNAs and piRNAs) associated with the RNA interference pathway small nuclear RNAs, small nucleolar and tRNAs derived small RNAs other types of small RNAs, such as those associated with splice junctions and transcription start sites long non-coding RNAs, including antisense RNAs, long ''intergenic'' RNAs, intronic RNAs and ''enhancer'' RNAs other classes of RNAs such as vault RNAs, scaRNAs, circular RNAs, 7SL RNAs, telomeric and centromeric RNAs regulatory functions of mRNAs and UTR-derived RNAs catalytic and allosteric (riboswitch) RNAs viral, transposon and repeat-derived RNAs bacterial regulatory RNAs, including CRISPR RNAS Analysis of RNA processing, RNA binding proteins, RNA signaling and RNA interaction pathways: DICER AGO, PIWI and PIWI-like proteins other classes of RNA binding and RNA transport proteins RNA interactions with chromatin-modifying complexes RNA interactions with DNA and other RNAs the role of RNA in the formation and function of specialized subnuclear organelles and other aspects of cell biology intercellular and intergenerational RNA signaling RNA processing structure-function relationships in RNA complexes RNA analyses, informatics, tools and technologies: transcriptomic analyses and technologies development of tools and technologies for RNA biology and therapeutics Translational studies involving long and short non-coding RNAs: identification of biomarkers development of new therapies involving microRNAs and other ncRNAs clinical studies involving microRNAs and other ncRNAs.
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