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Purification of H3 and H4 Histone Proteins and the Quantification of Acetylated Histone Marks in Cells and Brain Tissue
Published on: November 30, 2018
Epigenetic histone acetylation modifiers in vascular remodelling: new targets for therapy in cardiovascular disease
Douwe Pons1, Florentine R de Vries, Peter J van den Elsen
1Department of Cardiology, Leiden University Medical Center, C5-P, PO Box 9600, 2300 RC Leiden, The Netherlands.
Insights
Epigenetic mechanisms like histone acetylation and DNA methylation are key in cardiovascular diseases such as atherosclerosis and restenosis. Targeting these reversible epigenetic changes offers a promising new therapeutic strategy.
Area of Science:
- Cardiovascular Science
- Epigenetics
- Molecular Biology
Background:
- Current treatments for atherosclerosis and restenosis show limited efficacy due to disease heterogeneity and incomplete understanding of underlying mechanisms.
- Epigenetic mechanisms, including histone acetylation and DNA methylation, regulate gene expression without altering DNA sequence, influencing cellular processes.
- These epigenetic processes are implicated in extracellular matrix formation, inflammation, and proliferation, all critical in cardiovascular pathologies.
Purpose of the Study:
- To review the role of epigenetic regulators in the pathogenesis of atherosclerosis and restenosis.
- To highlight the potential of targeting epigenetic modifications for novel cardiovascular disease therapies.
Main Methods:
- Review of current literature on epigenetic mechanisms in cardiovascular diseases.
- Analysis of the role of histone acetylating and deacetylating enzymes in disease development.
- Examination of the reversibility of epigenetic alterations for therapeutic potential.
Main Results:
- Epigenetic regulators, specifically those controlling histone acetylation and deacetylation, are significantly involved in the development of atherosclerosis and restenosis.
- Alterations in chromatin structure mediated by these epigenetic factors contribute to disease pathogenesis.
- The reversible nature of these epigenetic modifications suggests they are druggable targets.
Conclusions:
- Epigenetic modifications are crucial contributors to the pathogenesis of atherosclerosis and restenosis.
- Pharmacological interventions targeting epigenetic regulators represent a potential new avenue for managing cardiovascular diseases.
- Further research into epigenetic therapies could lead to improved treatment outcomes for patients with these conditions.
Abstract:
Significant progress has been made in the clinical management of a variety of cardiovascular diseases. Nevertheless, the therapeutic efficacy of the current treatment modalities for atherosclerosis and restenosis is not fully sufficient in a large proportion of patients. One of the major contributing factors is the clinical and biological heterogeneity of these still life-threatening diseases, which involve processes that we do not fully understand at the moment. Over the past decades, it has become increasingly clear that part of the gene-environmental interactions relevant for complex diseases is regulated by epigenetic mechanisms such as histone acetylation and DNA methylation. Epigenetic processes modulate gene expression patterns without modifying the actual DNA sequence and have profound effects on the cellular repertoire of expressed genes. They contribute to the expression of genes that play a key role in extracellular matrix formation, inflammation, and proliferation, processes involved in cardiovascular pathologies such as atherosclerosis and restenosis. Therefore, in this review, we argue that epigenetic regulators involved in histone acetylating and deacetylating activities contribute to the pathogenesis of atherosclerosis and restenosis. Furthermore, as alterations in chromatin structure are reversible, these epigenetic modifications are amendable to pharmacological intervention, which may prove to be an effective treatment modality for the management of cardiovascular diseases.
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