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The Role of KLF2 in the Regulation of Atherosclerosis Development and Potential Use of KLF2-Targeted Therapy.

作者信息

Dabravolski Siarhei A, Sukhorukov Vasily N, Kalmykov Vladislav A, Grechko Andrey V, Shakhpazyan Nikolay K, Orekhov Alexander N

机构信息

Department of Clinical Diagnostics, Vitebsk State Academy of Veterinary Medicine [UO VGAVM], 7/11 Dovatora Str., 210026 Vitebsk, Belarus.

Laboratory of Cellular and Molecular Pathology of Cardiovascular System, AP Avtsyn Research Institute of Human Morphology, 3 Tsyurupy Str., 117418 Moscow, Russia.

出版信息

Biomedicines. 2022 Jan 24;10(2):254. doi: 10.3390/biomedicines10020254.


DOI:10.3390/biomedicines10020254
PMID:35203463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8869605/
Abstract

Kruppel like factor 2 (KLF2) is a mechanosensitive transcription factor participating in the regulation of vascular endothelial cells metabolism. Activating KLF2 in endothelial cells induces eNOS (endothelial nitric oxide synthase) expression, subsequent NO (nitric oxide) release, and vasodilatory effect. In addition, many KLF2-regulated genes participate in the anti-thrombotic, antioxidant, and anti-inflammatory activities, thereby preventing atherosclerosis development and progression. In this review, we summarise recent evidence suggesting that KLF2 plays a major role in regulating atheroprotective effects in endothelial cells. We also discuss several recently identified repurposed drugs and natural plant-based bioactive compounds with KLF2-mediated atheroprotective activities. Herein, we present a comprehensive overview of the role of KLF2 in atherosclerosis and as a pharmacological target for different drugs and natural compounds and highlight the potential application of these phytochemicals for the treatment of atherosclerosis.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40be/8869605/cea3b9331b80/biomedicines-10-00254-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40be/8869605/3942ae9e97ca/biomedicines-10-00254-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40be/8869605/cea3b9331b80/biomedicines-10-00254-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40be/8869605/3942ae9e97ca/biomedicines-10-00254-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40be/8869605/cea3b9331b80/biomedicines-10-00254-g002.jpg

相似文献

[1]
The Role of KLF2 in the Regulation of Atherosclerosis Development and Potential Use of KLF2-Targeted Therapy.

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本文引用的文献

[1]
Modulation of endothelium function by fatty acids.

Mol Cell Biochem. 2022-1

[2]
Disturbed flow's impact on cellular changes indicative of vascular aneurysm initiation, expansion, and rupture: A pathological and methodological review.

J Cell Physiol. 2022-1

[3]
The Role of Mitochondria-Derived Peptides in Cardiovascular Diseases and Their Potential as Therapeutic Targets.

Int J Mol Sci. 2021-8-16

[4]
Investigation of Wall Shear Stress in Cardiovascular Research and in Clinical Practice-From Bench to Bedside.

Int J Mol Sci. 2021-5-26

[5]
Chrysin boosts KLF2 expression through suppression of endothelial cell-derived exosomal microRNA-92a in the model of atheroprotection.

Eur J Nutr. 2021-12

[6]
A20/TNFAIP3 Increases ENOS Expression in an ERK5/KLF2-Dependent Manner to Support Endothelial Cell Health in the Face of Inflammation.

Front Cardiovasc Med. 2021-5-7

[7]
Azilsartan ameliorates ox-LDL-induced endothelial dysfunction via promoting the expression of KLF2.

Aging (Albany NY). 2021-5-4

[8]
Metformin attenuates atherosclerosis and plaque vulnerability by upregulating KLF2-mediated autophagy in apoE mice.

Biochem Biophys Res Commun. 2021-6-11

[9]
Shear-Regulated Extracellular Microenvironments and Endothelial Cell Surface Integrin Receptors Intertwine in Atherosclerosis.

Front Cell Dev Biol. 2021-4-6

[10]
Potential roles of Kruppel-like factors in mediating adverse vascular effects of nanomaterials: A review.

J Appl Toxicol. 2022-1

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