2024
DOI: 10.1620/tjem.2023.j097
|View full text |Cite
|
Sign up to set email alerts
|

Serum Exosomal MicroRNA-186-5p Positively Correlates with Lipid Indexes, Coronary Stenosis Degree, and Major Adverse Cardiovascular Events in Coronary Heart Disease

Lingyun Ren,
Wei Liu,
Shanshan Chen
et al.

Abstract: Serum exosomal microRNA-186-5p positively correlates with lipid indexes, coronary stenosis degree, and major adverse cardiovascular events in coronary heart disease

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2024
2024
2024
2024

Publication Types

Select...
1

Relationship

1
0

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 32 publications
0
1
0
Order By: Relevance
“…Regarding miR-186-5p, a previous study indicates that serum exosomal miR-186-5p shows a good diagnostic performance for AMI, and its dysregulation in exosomes contributes to atherosclerosis by targeting lectin-like ox-LDL receptor-1 (LOX-1) ( 15 ). Additionally, another study reports that serum exosomal miR-186-5p is positively associated with lipid level, coronary stenosis degree, and MACE risk in coronary heart disease patients ( 16 ). Inspiringly, our recently published study observes that macrophages-delivered exosomal miR-186-5p inactivates the Src homology 2-containing inositol 5-phosphatase 2 (SHIP2)-mediated phosphatidylinositol 3-kinase (PI3 K)/protein kinase B (AKT)/mammalian target of rapamycin (mTOR) pathway to facilitate vascular smooth muscle cell (VSMC) viability and invasion, thereby promoting atherogenesis ( 17 ).…”
Section: Introductionmentioning
confidence: 99%
“…Regarding miR-186-5p, a previous study indicates that serum exosomal miR-186-5p shows a good diagnostic performance for AMI, and its dysregulation in exosomes contributes to atherosclerosis by targeting lectin-like ox-LDL receptor-1 (LOX-1) ( 15 ). Additionally, another study reports that serum exosomal miR-186-5p is positively associated with lipid level, coronary stenosis degree, and MACE risk in coronary heart disease patients ( 16 ). Inspiringly, our recently published study observes that macrophages-delivered exosomal miR-186-5p inactivates the Src homology 2-containing inositol 5-phosphatase 2 (SHIP2)-mediated phosphatidylinositol 3-kinase (PI3 K)/protein kinase B (AKT)/mammalian target of rapamycin (mTOR) pathway to facilitate vascular smooth muscle cell (VSMC) viability and invasion, thereby promoting atherogenesis ( 17 ).…”
Section: Introductionmentioning
confidence: 99%