Literature DB >> 28259753

Long noncoding RNAs (LncRNAs) - The dawning of a new treatment for cardiac hypertrophy and heart failure.

Dong Han1, Quansheng Gao2, Feng Cao3.   

Abstract

Long noncoding RNAs (lncRNAs) represent a category of noncoding RNAs with the potential for genetic and epigenetic regulations. As important regulators of gene expression, increasing evidence has proven that lncRNAs play a significant regulatory role in various cardiovascular pathologies. In particular, lncRNAs have been proved to be participating in gene regulatory mechanisms involved in heart growth and development that can be exploited to repair the injured adult heart. Furthermore, lncRNAs have been revealed as possible therapeutic targets for heart failure with different causes and in different stages. In the journey from a healthy heart to heart failure, lncRNAs have been shown to participate in almost every landmark of heart failure pathogenesis including ischemic injury, cardiac hypertrophy, and cardiac fibrosis. Furthermore, the manipulation of lncRNAs palliates the progression of heart failure by attenuating ischemic heart injury, cardiac hypertrophy and cardiac fibrosis, as well as facilitating heart regeneration and therapeutic angiogenesis. This review will highlight recent updates regarding the involvement of lncRNAs in cardiac hypertrophy and heart failure and their potential as novel therapeutic targets. This article is part of a Special Issue entitled: Genetic and epigenetic control of heart failure - edited by Jun Ren & Megan Yingmei Zhang.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Biomarker; Genetic; Heart failure; Hypertrophy; Ischemic heart disease; Long noncoding RNAs; Treatment

Mesh:

Substances:

Year:  2017        PMID: 28259753     DOI: 10.1016/j.bbadis.2017.02.024

Source DB:  PubMed          Journal:  Biochim Biophys Acta Mol Basis Dis        ISSN: 0925-4439            Impact factor:   5.187


  7 in total

1.  LncRNA TUG1 contributes to cardiac hypertrophy via regulating miR-29b-3p.

Authors:  Xue Zou; Jialiang Wang; Li Tang; Qian Wen
Journal:  In Vitro Cell Dev Biol Anim       Date:  2019-06-10       Impact factor: 2.416

Review 2.  Epigenetic signatures in cardiac fibrosis, special emphasis on DNA methylation and histone modification.

Authors:  Hui Tao; Zheng-Yu Song; Xuan-Sheng Ding; Jing-Jing Yang; Kai-Hu Shi; Jun Li
Journal:  Heart Fail Rev       Date:  2018-09       Impact factor: 4.214

3.  Relationship between lncRNA-Ang362 and prognosis of patients with coronary heart disease after percutaneous coronary intervention.

Authors:  Hui Wang; Huichao Gong; Yingwu Liu; Limin Feng
Journal:  Biosci Rep       Date:  2020-07-31       Impact factor: 3.840

4.  Silencing long non-coding RNA MIAT ameliorates myocardial dysfunction induced by myocardial infarction via MIAT/miR-10a-5p/EGR2 axis.

Authors:  Xiangke Cao; Qinghua Ma; Bin Wang; Qingqiang Qian; Ning Liu; Tiejun Liu; Xiaoliu Dong
Journal:  Aging (Albany NY)       Date:  2021-03-26       Impact factor: 5.682

Review 5.  Long non-coding RNAs and microRNAs as crucial regulators in cardio-oncology.

Authors:  Sarath Babu Nukala; Jordan Jousma; Yoonje Cho; Won Hee Lee; Sang-Ging Ong
Journal:  Cell Biosci       Date:  2022-03-04       Impact factor: 7.133

6.  RNA binding Motif protein-38 regulates myocardial hypertrophy in LXR-α-dependent lipogenesis pathway.

Authors:  Yao Li; Yanhu Shi; Yaoli He; Xiaoming Li; Junlu Yang
Journal:  Bioengineered       Date:  2021-12       Impact factor: 3.269

7.  A Novel Class of tRNA-Derived Small Non-Coding RNAs Respond to Myocardial Hypertrophy and Contribute to Intergenerational Inheritance.

Authors:  Linyuan Shen; Mailin Gan; Zhengdong Tan; Dongmei Jiang; Yanzhi Jiang; Mingzhou Li; Jinyong Wang; Xuewei Li; Shunhua Zhang; Li Zhu
Journal:  Biomolecules       Date:  2018-07-16
  7 in total

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