Serum‑derived exosomal hsa‑let‑7b‑5p as a biomarker for predicting the severity of coronary stenosis in patients with coronary heart disease and hyperglycemia.


Journal

Molecular medicine reports
ISSN: 1791-3004
Titre abrégé: Mol Med Rep
Pays: Greece
ID NLM: 101475259

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 22 03 2023
accepted: 21 08 2023
medline: 18 9 2023
pubmed: 15 9 2023
entrez: 15 9 2023
Statut: ppublish

Résumé

Exosomal microRNAs (miRNAs/miRs) are potential biomarkers for the diagnosis and treatment of cardiovascular disease, and hyperglycemia serves an important role in the development of atherosclerosis. The present study aimed to investigate the expression profile of serum‑derived exosomal miRNAs in coronary heart disease (CHD) with hyperglycemia, and to identify effective biomarkers for predicting coronary artery lesions. Serum samples were collected from eight patients with CHD and hyperglycemia and eight patients with CHD and normoglycemia, exosomes were isolated and differentially expressed miRNAs (DEMIs) were filtered using a human miRNA microarray. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses were performed using standard enrichment computational methods for the target genes of DEMIs. Receiver operating characteristic (ROC) curve analysis was applied to evaluate the values of the selected DEMIs in predicting the severity of coronary stenosis. A total of 10 DEMIs, including four upregulated miRNAs (hsa‑let‑7b‑5p, hsa‑miR‑4313, hsa‑miR‑4665‑3p and hsa‑miR‑940) and six downregulated miRNAs (hsa‑miR‑4459, hsa‑miR‑4687‑3p, hsa‑miR‑6087, hsa‑miR‑6089, hsa‑miR‑6740‑5p and hsa‑miR‑6800‑5p), were screened in patients with CHD and hyperglycemia. GO analysis showed that the 'cellular process', 'single‑organism process' and 'biological regulation' were significantly enriched. KEGG pathway analysis revealed that the 'mTOR signaling pathway', 'FoxO signaling pathway' and 'neurotrophin signaling pathway' were significantly enriched. Among these DEMIs, only hsa‑let‑7b‑5p expression was positively correlated with both hemoglobin A1C levels and Synergy between Percutaneous Coronary Intervention with Taxus and Cardiac Surgery score. ROC curves showed that hsa‑let‑7b‑5p could serve as an effective biomarker for differentiating the severity of coronary stenosis. In conclusion, the present study demonstrated that serum‑derived exosomal hsa‑let‑7b‑5p is upregulated in patients with CHD and hyperglycemia, and may serve as a noninvasive biomarker for the severity of coronary stenosis.

Identifiants

pubmed: 37711034
doi: 10.3892/mmr.2023.13090
pii: 203
pmc: PMC10539999
doi:
pii:

Substances chimiques

Biomarkers 0
MicroRNAs 0
mirnlet7 microRNA, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Shufang Han (S)

Department of Cardiology, The 960th Hospital of The Joint Service Support Force of The People's Liberation Army, Jinan, Shandong 250031, P.R. China.

Jie Fang (J)

Department of Cardiology, The 960th Hospital of The Joint Service Support Force of The People's Liberation Army, Jinan, Shandong 250031, P.R. China.

Lili Yu (L)

Department of Cardiology, The 960th Hospital of The Joint Service Support Force of The People's Liberation Army, Jinan, Shandong 250031, P.R. China.

Bin Li (B)

Department of Cardiology, The 960th Hospital of The Joint Service Support Force of The People's Liberation Army, Jinan, Shandong 250031, P.R. China.

Yuhong Hu (Y)

Department of Cardiology, The 960th Hospital of The Joint Service Support Force of The People's Liberation Army, Jinan, Shandong 250031, P.R. China.

Ruimin Chen (R)

Department of Cardiology, The 960th Hospital of The Joint Service Support Force of The People's Liberation Army, Jinan, Shandong 250031, P.R. China.

Changyong Li (C)

Department of Cardiology, The 960th Hospital of The Joint Service Support Force of The People's Liberation Army, Jinan, Shandong 250031, P.R. China.

Chuanxu Zhao (C)

Department of Cardiology, The 960th Hospital of The Joint Service Support Force of The People's Liberation Army, Jinan, Shandong 250031, P.R. China.

Jiaying Li (J)

Department of Cardiology, The 960th Hospital of The Joint Service Support Force of The People's Liberation Army, Jinan, Shandong 250031, P.R. China.

Yinan Wang (Y)

Department of Cardiology, The 960th Hospital of The Joint Service Support Force of The People's Liberation Army, Jinan, Shandong 250031, P.R. China.

Yuqi Gao (Y)

Department of Cardiology, The 960th Hospital of The Joint Service Support Force of The People's Liberation Army, Jinan, Shandong 250031, P.R. China.

Hong Tan (H)

Department of Cardiology, The 960th Hospital of The Joint Service Support Force of The People's Liberation Army, Jinan, Shandong 250031, P.R. China.

Qun Jin (Q)

Department of Cardiology, The 960th Hospital of The Joint Service Support Force of The People's Liberation Army, Jinan, Shandong 250031, P.R. China.

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Classifications MeSH