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The Endothelium as a Target for Anti-Atherogenic Therapy: A Focus on the Epigenetic Enzymes EZH2 and SIRT1

Endothelial cell inflammatory activation and dysfunction are key events in the pathophysiology of atherosclerosis, and are associated with an elevated risk of cardiovascular events. Yet, therapies specifically targeting the endothelium and atherosclerosis are lacking. Here, we review how endothelial...

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Autores principales: Fledderus, Jolien, Vanchin, Byambasuren, Rots, Marianne G., Krenning, Guido
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7915331/
https://www.ncbi.nlm.nih.gov/pubmed/33562658
http://dx.doi.org/10.3390/jpm11020103
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author Fledderus, Jolien
Vanchin, Byambasuren
Rots, Marianne G.
Krenning, Guido
author_facet Fledderus, Jolien
Vanchin, Byambasuren
Rots, Marianne G.
Krenning, Guido
author_sort Fledderus, Jolien
collection PubMed
description Endothelial cell inflammatory activation and dysfunction are key events in the pathophysiology of atherosclerosis, and are associated with an elevated risk of cardiovascular events. Yet, therapies specifically targeting the endothelium and atherosclerosis are lacking. Here, we review how endothelial behaviour affects atherogenesis and pose that the endothelium may be an efficacious cellular target for antiatherogenic therapies. We discuss the contribution of endothelial inflammatory activation and dysfunction to atherogenesis and postulate that the dysregulation of specific epigenetic enzymes, EZH2 and SIRT1, aggravate endothelial dysfunction in a pleiotropic fashion. Moreover, we propose that commercially available drugs are available to clinically explore this postulation.
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spelling pubmed-79153312021-03-01 The Endothelium as a Target for Anti-Atherogenic Therapy: A Focus on the Epigenetic Enzymes EZH2 and SIRT1 Fledderus, Jolien Vanchin, Byambasuren Rots, Marianne G. Krenning, Guido J Pers Med Review Endothelial cell inflammatory activation and dysfunction are key events in the pathophysiology of atherosclerosis, and are associated with an elevated risk of cardiovascular events. Yet, therapies specifically targeting the endothelium and atherosclerosis are lacking. Here, we review how endothelial behaviour affects atherogenesis and pose that the endothelium may be an efficacious cellular target for antiatherogenic therapies. We discuss the contribution of endothelial inflammatory activation and dysfunction to atherogenesis and postulate that the dysregulation of specific epigenetic enzymes, EZH2 and SIRT1, aggravate endothelial dysfunction in a pleiotropic fashion. Moreover, we propose that commercially available drugs are available to clinically explore this postulation. MDPI 2021-02-05 /pmc/articles/PMC7915331/ /pubmed/33562658 http://dx.doi.org/10.3390/jpm11020103 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Fledderus, Jolien
Vanchin, Byambasuren
Rots, Marianne G.
Krenning, Guido
The Endothelium as a Target for Anti-Atherogenic Therapy: A Focus on the Epigenetic Enzymes EZH2 and SIRT1
title The Endothelium as a Target for Anti-Atherogenic Therapy: A Focus on the Epigenetic Enzymes EZH2 and SIRT1
title_full The Endothelium as a Target for Anti-Atherogenic Therapy: A Focus on the Epigenetic Enzymes EZH2 and SIRT1
title_fullStr The Endothelium as a Target for Anti-Atherogenic Therapy: A Focus on the Epigenetic Enzymes EZH2 and SIRT1
title_full_unstemmed The Endothelium as a Target for Anti-Atherogenic Therapy: A Focus on the Epigenetic Enzymes EZH2 and SIRT1
title_short The Endothelium as a Target for Anti-Atherogenic Therapy: A Focus on the Epigenetic Enzymes EZH2 and SIRT1
title_sort endothelium as a target for anti-atherogenic therapy: a focus on the epigenetic enzymes ezh2 and sirt1
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7915331/
https://www.ncbi.nlm.nih.gov/pubmed/33562658
http://dx.doi.org/10.3390/jpm11020103
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