» Articles » PMID: 35529430

New Insight in HDACs: Potential Therapeutic Targets for the Treatment of Atherosclerosis

Overview
Journal Front Pharmacol
Date 2022 May 9
PMID 35529430
Authors
Affiliations
Soon will be listed here.
Abstract

Atherosclerosis (AS) features include progressive hardening and reduced elasticity of arteries. AS is the leading cause of morbidity and mortality. An increasing amount of evidence showed that epigenetic modifications on genes serve are a main cause of several diseases, including AS. Histone deacetylases (HDACs) promote the deacetylation at lysine residues, thereby condensing the chromatin structures and further inhibiting the transcription of downstream genes. HDACs widely affect various physiological and pathological processes through transcriptional regulation or deacetylation of other non-histone proteins. In recent years, the role of HDACs in vascular systems has been revealed, and their effects on atherosclerosis have been widely reported. In this review, we discuss the members of HDACs in vascular systems, determine the diverse roles of HDACs in AS, and reveal the effects of HDAC inhibitors on AS progression. We provide new insights into the potential of HDAC inhibitors as drugs for AS treatment.

Citing Articles

Knockdown of USP7 alleviates atherosclerosis in ApoE-deficient mice by regulating EZH2 expression.

Zhang Y, Zhang Y Open Life Sci. 2024; 19(1):20220929.

PMID: 39310812 PMC: 11416069. DOI: 10.1515/biol-2022-0929.


Zinc-Dependent Histone Deacetylases in Lung Endothelial Pathobiology.

Patil R, Maloney M, Lucas R, Fulton D, Patel V, Bagi Z Biomolecules. 2024; 14(2).

PMID: 38397377 PMC: 10886568. DOI: 10.3390/biom14020140.


Cardiac cell senescence: molecular mechanisms, key proteins and therapeutic targets.

Luan Y, Zhu X, Jiao Y, Liu H, Huang Z, Pei J Cell Death Discov. 2024; 10(1):78.

PMID: 38355681 PMC: 10866973. DOI: 10.1038/s41420-023-01792-5.


Deacetylation of Histones and Non-histone Proteins in Inflammatory Diseases and Cancer Therapeutic Potential of Histone Deacetylase Inhibitors.

Man E, Evran S Curr Genomics. 2024; 24(3):136-145.

PMID: 38178983 PMC: 10761333. DOI: 10.2174/0113892029265046231011100327.


PRC2-dependent regulation of ganglioside expression during dedifferentiation contributes to the proliferation and migration of vascular smooth muscle cells.

Sasaki N, Hirano K, Shichi Y, Itakura Y, Ishiwata T, Toyoda M Front Cell Dev Biol. 2022; 10:1003349.

PMID: 36313564 PMC: 9606594. DOI: 10.3389/fcell.2022.1003349.

References
1.
Wang X, Cao K, Sun X, Chen Y, Duan Z, Sun L . Macrophages in spinal cord injury: phenotypic and functional change from exposure to myelin debris. Glia. 2014; 63(4):635-51. PMC: 4331228. DOI: 10.1002/glia.22774. View

2.
Hou J, Wang S, Shang Y, Chong Z, Maiese K . Erythropoietin employs cell longevity pathways of SIRT1 to foster endothelial vascular integrity during oxidant stress. Curr Neurovasc Res. 2011; 8(3):220-35. PMC: 3149772. DOI: 10.2174/156720211796558069. View

3.
Rajendrasozhan S, Yang S, Edirisinghe I, Yao H, Adenuga D, Rahman I . Deacetylases and NF-kappaB in redox regulation of cigarette smoke-induced lung inflammation: epigenetics in pathogenesis of COPD. Antioxid Redox Signal. 2008; 10(4):799-811. PMC: 2758554. DOI: 10.1089/ars.2007.1938. View

4.
Qin B, Shu Y, Xiao L, Lu T, Lin Y, Yang H . MicroRNA-150 targets ELK1 and modulates the apoptosis induced by ox-LDL in endothelial cells. Mol Cell Biochem. 2017; 429(1-2):45-58. DOI: 10.1007/s11010-016-2935-3. View

5.
Li Y, Seto E . HDACs and HDAC Inhibitors in Cancer Development and Therapy. Cold Spring Harb Perspect Med. 2016; 6(10). PMC: 5046688. DOI: 10.1101/cshperspect.a026831. View