Low Levels of MicroRNA-10a in Cardiovascular Endothelium and Blood Serum Are Related to Human Atherosclerotic Disease.


Journal

Cardiology research and practice
ISSN: 2090-8016
Titre abrégé: Cardiol Res Pract
Pays: United States
ID NLM: 101516542

Informations de publication

Date de publication:
2021
Historique:
received: 22 04 2021
accepted: 30 06 2021
entrez: 2 8 2021
pubmed: 3 8 2021
medline: 3 8 2021
Statut: epublish

Résumé

MicroRNA-10a (miR-10a) inhibits transcriptional factor GATA6 to repress inflammatory GATA6/VCAM-1 signaling, which is regulated by blood flow to affect endothelial function/dysfunction. This study aimed to identify the expression patterns of miR-10a/GATA6/VCAM-1 Human atherosclerotic coronary arteries and nondiseased arteries were used to detect the expressions of miR-10a/GATA6/VCAM-1 in pathogenic The comparison of human atherosclerotic coronary arteries with nondiseased arteries demonstrated that lower levels of endothelial miR-10a are related to human atherogenesis. Moreover, GATA6/VCAM-1 (a downstream target of miR-10a) was highly expressed in the endothelium, accompanied by the reduced levels of miR-10a during the development of human atherosclerosis. In addition, CAD patients had a significantly lower concentration of miR-10a in their serum compared to healthy subjects. Our findings suggest that low miR-10a and high GATA6/VCAM-1 in the cardiovascular endothelium correlates to the development of human atherosclerotic lesions, suggesting that miR-10a signaling has the potential to be developed as a biomarker for human atherosclerosis.

Sections du résumé

BACKGROUND BACKGROUND
MicroRNA-10a (miR-10a) inhibits transcriptional factor GATA6 to repress inflammatory GATA6/VCAM-1 signaling, which is regulated by blood flow to affect endothelial function/dysfunction. This study aimed to identify the expression patterns of miR-10a/GATA6/VCAM-1
METHODS METHODS
Human atherosclerotic coronary arteries and nondiseased arteries were used to detect the expressions of miR-10a/GATA6/VCAM-1 in pathogenic
RESULTS RESULTS
The comparison of human atherosclerotic coronary arteries with nondiseased arteries demonstrated that lower levels of endothelial miR-10a are related to human atherogenesis. Moreover, GATA6/VCAM-1 (a downstream target of miR-10a) was highly expressed in the endothelium, accompanied by the reduced levels of miR-10a during the development of human atherosclerosis. In addition, CAD patients had a significantly lower concentration of miR-10a in their serum compared to healthy subjects.
CONCLUSIONS CONCLUSIONS
Our findings suggest that low miR-10a and high GATA6/VCAM-1 in the cardiovascular endothelium correlates to the development of human atherosclerotic lesions, suggesting that miR-10a signaling has the potential to be developed as a biomarker for human atherosclerosis.

Identifiants

pubmed: 34336268
doi: 10.1155/2021/1452917
pmc: PMC8298183
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1452917

Informations de copyright

Copyright © 2021 Jong-Tar Kuo et al.

Déclaration de conflit d'intérêts

The authors declare that there are no conflicts of interest.

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Auteurs

Jong-Tar Kuo (JT)

Department of Biological Science and Technology, China University of Science and Technology, Taipei, Taiwan.

Hsiao-En Tsai (HE)

Division of Cardiovascular Surgery, Department of Surgery, National Taiwan University Hsin-Chu Hospital, Hsinchu, Taiwan.
Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine, Taipei, Taiwan.

Ching-Ting Lin (CT)

School of Chinese Medicine, China Medical University, Taichung, Taiwan.

Chih-I Lee (CI)

Institute of Cellular and System Medicine, National Health Research Institutes, Miaoli, Taiwan.

Pei-Ling Lee (PL)

Institute of Cellular and System Medicine, National Health Research Institutes, Miaoli, Taiwan.

Yu-Rong Ruan (YR)

Department of Biological Science and Technology, China University of Science and Technology, Taipei, Taiwan.

Jeng-Jiann Chiu (JJ)

Institute of Cellular and System Medicine, National Health Research Institutes, Miaoli, Taiwan.

Ding-Yu Lee (DY)

Department of Biological Science and Technology, China University of Science and Technology, Taipei, Taiwan.

Classifications MeSH