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Prostaglandin E2 (Pge2) Synthesis Pathway Is Involved in Coronary Artery Stenosis and Restenosis Publisher Pubmed



Kakavandi N1 ; Rezaee S1 ; Hosseinifard SR2 ; Ghasempour G1 ; Khosravi M3 ; Shabani M1 ; Najafi M1
Authors
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Authors Affiliations
  1. 1. Iran University of Medical Sciences, Medical School, Biochemistry Department, Iran
  2. 2. Tehran University of Medical Sciences, Biochemistry Department, Iran
  3. 3. Medicine Biochemistry, Qom Branch, Islamic Azad University, Qom, Iran

Source: Gene Published:2021


Abstract

The inflammatory events related to prostaglandins may play an important role in the progression of vessel stenosis. The aim of this study was to investigate the monocyte PTGES and 15-PGDH gene expression levels and the serum 13,14-dihyro-15-keto-PGF2α value involved in PGE2 metabolism in patients with coronary artery stenosis and restenosis. Moreover, the effects of miR-520, miR-1297 and miR-34 were studied on the gene expression levels. A total of sixty subjects referred for coronary angiography including healthy controls (stenosis <5%), subjects with stent no restenosis) SNR, stenosis <5%) and subjects in stent restenosis (ISR, restenosis >70%) were participated in the study. The gene expression levels and the serum 13,14-dihyro-15-keto- PGF2α value were measured by RT-qPCR and ELISA techniques, respectively. Moreover, the effects of miRNAs on the gene expression levels were investigated by the monocyte transfection of miR/PEI complexes. The PTGES and 15-PGDH gene expression levels and serum 13,14-dihyro-15-keto- PGF2α value increased significantly (P <0.05). Based on the miR-520 and miR-34 expression levels, the miR/PEI transfection studies were confirmed significantly the gene expression changes. The monocyte PGE2 synthesis pathway is actively considered in the SNR and ISR patients and might be related to miR-34 and miR-520 functions. © 2020