Non-coding RNAs as direct and indirect modulators of epigenetic mechanism regulation of cardiac fibrosis

被引:30
|
作者
Tao, Hui [1 ,2 ]
Yang, Jing-Jing [3 ]
Shi, Kai-Hu [1 ,2 ]
机构
[1] Anhui Med Univ, Hosp 2, Dept Cardiothorac Surg, Hefei 230601, Anhui, Peoples R China
[2] Anhui Med Univ, Cardiovasc Res Ctr, Hefei 230601, Peoples R China
[3] Anhui Med Univ, Hosp 2, Dept Pharmacol, Hefei 230601, Peoples R China
关键词
cardiac fibrosis; DNA methylation; epigenetic; histone modification; long non-coding RNA; microRNA; POLYCOMB-GROUP PROTEIN; DNA METHYLATION; GENE-EXPRESSION; GENOME REGULATION; LONG; MICRORNAS; HYPERTROPHY; REPRESSION; HISTONE; BINDING;
D O I
10.1517/14728222.2014.1001740
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Cardiac fibroblast activation is a pivotal cellular event in cardiac fibrosis. Numerous studies have indicated that epigenetic modifications control cardiac fibroblast activation. Greater knowledge of the role of epigenetic modifications could improve understanding of the cardiac fibrosis pathogenesis. Areas covered: The aim of this review is to describe the present knowledge about the important role of non-coding RNA (ncRNA) transcripts in epigenetic gene regulation in cardiac fibrosis and looks ahead on new perspectives of epigenetic modification research. Furthermore, we will discuss examples of ncRNAs that interact with histone modification or DNA methylation to regulate gene expression. Expert opinion: MicroRNAs (miRNAs) and long ncRNAs (lncRNAs) modulate several important aspects of function. Recently, some studies continue to find novel pathways, including the important role of ncRNA transcripts in epigenetic gene regulation. Targeting the miRNAs and lncRNAs can be a promising direction in cardiac fibrosis treatment. We discuss new perspectives of ncRNAs that interact with histone modification or DNA methylation to regulate gene expression, others that are targets of these epigenetic mechanisms. The emerging recognition of the diverse functions of ncRNAs in regulating gene expression by epigenetic mechanisms suggests that they may represent new targets for therapeutic intervention.
引用
收藏
页码:707 / 716
页数:10
相关论文
共 50 条
  • [31] Non-coding RNAs in Cardiac Regeneration
    Yuan, Ting
    Krishnan, Jaya
    [J]. FRONTIERS IN PHYSIOLOGY, 2021, 12
  • [32] Non-coding RNAs in Cardiac Regeneration
    van der Ven, C. F. T.
    Hogewoning, B. C. R.
    van Mil, A.
    Sluijter, Joost P. G.
    [J]. NON-CODING RNAS IN CARDIOVASCULAR DISEASES, 2020, 1229 : 163 - 180
  • [33] Non-Coding RNAs in Cardiac Aging
    Wang, Hui
    Bei, Yihua
    Shi, Jing
    Xiao, Junjie
    Kong, Xiangqing
    [J]. CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2015, 36 (05) : 1679 - 1687
  • [34] Non-coding RNAs and Cardiac Aging
    Zhao, Cuimei
    Li, Guoping
    Li, Jin
    [J]. NON-CODING RNAS IN CARDIOVASCULAR DISEASES, 2020, 1229 : 247 - 258
  • [35] Non-coding RNAs in cardiac hypertrophy
    Ottaviani, Lara
    da Costa Martins, Paula A.
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 2017, 595 (12): : 4037 - 4050
  • [36] Gene regulation by non-coding RNAs
    Patil, Veena S.
    Zhou, Rui
    Rana, Tariq M.
    [J]. CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2014, 49 (01) : 16 - 32
  • [37] Epigenetic regulation of RET receptor tyrosine kinase and non-coding RNAs in MTC
    Joo, Lauren Jin Suk
    Zhao, Jing Ting
    Gild, Matti L.
    Glover, Anthony R.
    Sidhu, Stan B.
    [J]. MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2018, 469 : 48 - 53
  • [38] Histone Modifications and Non-Coding RNAs: Mutual Epigenetic Regulation and Role in Pathogenesis
    Bure, Irina, V
    Nemtsova, Marina, V
    Kuznetsova, Ekaterina B.
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (10)
  • [39] Genetic regulation by non-coding RNAs
    Qi Liwang
    Li Xinmin
    Zhang Shougong
    An Daochang
    [J]. SCIENCE IN CHINA SERIES C-LIFE SCIENCES, 2006, 49 (03): : 201 - 217
  • [40] Non-coding RNAs in Transcriptional Regulation
    Yung-Chia Ariel Chen
    Alexei A. Aravin
    [J]. Current Molecular Biology Reports, 2015, 1 (1) : 10 - 18