Microarray meta-analysis reveals IL6 and p38β/MAPK11 as potential targets of hsa-miR-124 in endothelial progenitor cells: Implications for stent re-endothelization in diabetic patients.

circulating progenitor endothelial cells diabetes micro-RNA microarray meta-analysis stent restenosis

Journal

Frontiers in cardiovascular medicine
ISSN: 2297-055X
Titre abrégé: Front Cardiovasc Med
Pays: Switzerland
ID NLM: 101653388

Informations de publication

Date de publication:
2022
Historique:
received: 08 06 2022
accepted: 25 08 2022
entrez: 30 9 2022
pubmed: 1 10 2022
medline: 1 10 2022
Statut: epublish

Résumé

Circulating endothelial progenitor cells (EPCs) play an important role in the repair processes of damaged vessels, favoring re-endothelization of stented vessels to minimize restenosis. EPCs number and function is diminished in patients with type 2 diabetes, a known risk factor for restenosis. Considering the impact of EPCs in vascular injury repair, we conducted a meta-analysis of microarray to assess the transcriptomic profile and determine target genes during the differentiation process of EPCs into mature ECs. Five microarray datasets, including 13 EPC and 12 EC samples were analyzed, using the online tool ExpressAnalyst. Differentially expressed genes (DEGs) analysis was done by Limma method, with an | log

Identifiants

pubmed: 36176980
doi: 10.3389/fcvm.2022.964721
pmc: PMC9513120
doi:

Types de publication

Journal Article

Langues

eng

Pagination

964721

Informations de copyright

Copyright © 2022 Arencibia and Salazar.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Alberto Arencibia (A)

Department of Basic Sciences, Faculty of Medicine, Center of Molecular Biology and Pharmacogenetics, Universidad de La Frontera, Temuco, Chile.

Luis A Salazar (LA)

Department of Basic Sciences, Faculty of Medicine, Center of Molecular Biology and Pharmacogenetics, Universidad de La Frontera, Temuco, Chile.

Classifications MeSH