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Published on: November 2, 2020
Epigenetics in Cardiac Hypertrophy and Heart Failure
Chia-Feng Liu1, W H Wilson Tang1,2
1Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio.
Epigenetic regulators offer therapeutic potential for heart failure (HF). This review summarizes epigenomic studies in human and animal models, highlighting DNA methylation, histone modifications, chromatin remodeling, and non-coding RNAs in HF pathophysiology.
Area of Science:
- Cardiovascular Research
- Molecular Biology
- Genetics
Background:
- Heart failure (HF) is a global health challenge affecting millions.
- Epigenetic dysregulation is increasingly recognized in HF pathogenesis.
- Targeting epigenetic mechanisms presents a promising therapeutic avenue for HF.
Purpose of the Study:
- To review the current understanding of epigenomic alterations in heart failure.
- To summarize findings from human and animal studies on epigenetics in HF.
- To highlight the role of specific epigenetic mechanisms in HF pathophysiology.
Main Methods:
- Comprehensive literature search of epigenomic studies in HF.
- Analysis of studies focusing on DNA methylation, histone modifications, chromatin remodeling, and non-coding RNAs.
- Inclusion of both human and animal model data.
Main Results:
- Next-generation sequencing has advanced the understanding of epigenomic roles in HF.
- Key epigenetic modifications, including DNA methylation and histone alterations, are implicated in HF.
- Non-coding RNAs and ATP-dependent chromatin remodeling are critical in HF development.
Conclusions:
- Epigenetic regulation plays a significant role in heart failure.
- Understanding these mechanisms is crucial for developing novel HF therapies.
- Further research into epigenomic targets holds potential for effective HF treatment.
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