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Yes-Associated Protein in Atherosclerosis and Related Complications: A Potential Therapeutic Target That Requires Further Exploration

Atherosclerosis and its complications diseases remain leading causes of cardiovascular morbidity and mortality, bringing a massive burden on public health worldwide. Atherosclerosis is recognized as chronic inflammation, and involves several highly correlated processes, including lipid metabolism dy...

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Autores principales: Sun, Congrui, He, Bin, Sun, Mingsheng, Lv, Xiaoshuo, Wang, Feng, Chen, Jie, Zhang, Jianbin, Ye, Zhidong, Wen, Jianyan, Liu, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8430249/
https://www.ncbi.nlm.nih.gov/pubmed/34513949
http://dx.doi.org/10.3389/fcvm.2021.704208
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author Sun, Congrui
He, Bin
Sun, Mingsheng
Lv, Xiaoshuo
Wang, Feng
Chen, Jie
Zhang, Jianbin
Ye, Zhidong
Wen, Jianyan
Liu, Peng
author_facet Sun, Congrui
He, Bin
Sun, Mingsheng
Lv, Xiaoshuo
Wang, Feng
Chen, Jie
Zhang, Jianbin
Ye, Zhidong
Wen, Jianyan
Liu, Peng
author_sort Sun, Congrui
collection PubMed
description Atherosclerosis and its complications diseases remain leading causes of cardiovascular morbidity and mortality, bringing a massive burden on public health worldwide. Atherosclerosis is recognized as chronic inflammation, and involves several highly correlated processes, including lipid metabolism dysfunction, endothelial cell dysfunction, inflammation, oxidative stress, vascular smooth muscle cell activation, platelet activation, thrombosis, altered matrix metabolism, and vascular remodeling. Within the past few decades, accumulating evidence has shown that the Yes-associated protein (YAP), the major effector of the Hippo pathway, can play a crucial role in pathogenesis and development of atherosclerosis. Activation of YAP-related pathways, which are induced by alerting flow pattern and matrix stiffness among others, can regulate processes including vascular endothelial cell dysfunction, monocyte infiltration, and smooth muscle cell migration, which contribute to atherosclerotic lesion formation. Further, YAP potentially modulates atherosclerotic complications such as vascular calcification and intraplaque hemorrhage, which require further investigation. Here, we summarized the relevant literature to outline current findings detailing the relationship between of YAP and atherosclerosis and highlight areas for future research.
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spelling pubmed-84302492021-09-11 Yes-Associated Protein in Atherosclerosis and Related Complications: A Potential Therapeutic Target That Requires Further Exploration Sun, Congrui He, Bin Sun, Mingsheng Lv, Xiaoshuo Wang, Feng Chen, Jie Zhang, Jianbin Ye, Zhidong Wen, Jianyan Liu, Peng Front Cardiovasc Med Cardiovascular Medicine Atherosclerosis and its complications diseases remain leading causes of cardiovascular morbidity and mortality, bringing a massive burden on public health worldwide. Atherosclerosis is recognized as chronic inflammation, and involves several highly correlated processes, including lipid metabolism dysfunction, endothelial cell dysfunction, inflammation, oxidative stress, vascular smooth muscle cell activation, platelet activation, thrombosis, altered matrix metabolism, and vascular remodeling. Within the past few decades, accumulating evidence has shown that the Yes-associated protein (YAP), the major effector of the Hippo pathway, can play a crucial role in pathogenesis and development of atherosclerosis. Activation of YAP-related pathways, which are induced by alerting flow pattern and matrix stiffness among others, can regulate processes including vascular endothelial cell dysfunction, monocyte infiltration, and smooth muscle cell migration, which contribute to atherosclerotic lesion formation. Further, YAP potentially modulates atherosclerotic complications such as vascular calcification and intraplaque hemorrhage, which require further investigation. Here, we summarized the relevant literature to outline current findings detailing the relationship between of YAP and atherosclerosis and highlight areas for future research. Frontiers Media S.A. 2021-08-27 /pmc/articles/PMC8430249/ /pubmed/34513949 http://dx.doi.org/10.3389/fcvm.2021.704208 Text en Copyright © 2021 Sun, He, Sun, Lv, Wang, Chen, Zhang, Ye, Wen and Liu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cardiovascular Medicine
Sun, Congrui
He, Bin
Sun, Mingsheng
Lv, Xiaoshuo
Wang, Feng
Chen, Jie
Zhang, Jianbin
Ye, Zhidong
Wen, Jianyan
Liu, Peng
Yes-Associated Protein in Atherosclerosis and Related Complications: A Potential Therapeutic Target That Requires Further Exploration
title Yes-Associated Protein in Atherosclerosis and Related Complications: A Potential Therapeutic Target That Requires Further Exploration
title_full Yes-Associated Protein in Atherosclerosis and Related Complications: A Potential Therapeutic Target That Requires Further Exploration
title_fullStr Yes-Associated Protein in Atherosclerosis and Related Complications: A Potential Therapeutic Target That Requires Further Exploration
title_full_unstemmed Yes-Associated Protein in Atherosclerosis and Related Complications: A Potential Therapeutic Target That Requires Further Exploration
title_short Yes-Associated Protein in Atherosclerosis and Related Complications: A Potential Therapeutic Target That Requires Further Exploration
title_sort yes-associated protein in atherosclerosis and related complications: a potential therapeutic target that requires further exploration
topic Cardiovascular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8430249/
https://www.ncbi.nlm.nih.gov/pubmed/34513949
http://dx.doi.org/10.3389/fcvm.2021.704208
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