Plasma miR-18 Screens Acute Myocardial Infarction from Healthy Controls by Targeting Hypoxia Inducible Factor 1α

被引:5
|
作者
Jiang, Meng [1 ]
Yin, Yutong [1 ]
Xie, Lianna [1 ]
He, Huozhen [2 ]
机构
[1] Danlian Univ, Dept Cardiol, Zhongshan Hosp, Dalian 116001, Liaoning, Peoples R China
[2] Dalian Univ, Dept Resp Med, Zhongshan Hosp, Jiefang St 6, Dalian 116001, Liaoning, Peoples R China
关键词
acute myocardial infarction; plasma miR-18; HIF1; alpha; biomarker; ENDOTHELIAL GROWTH-FACTOR; DOWN-REGULATION; RATS ROLE; BIOMARKER; EXPRESSION; DIAGNOSIS; MICRORNA; MIR-208B; CELLS;
D O I
10.7754/Clin.Lab.2018.180208
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: This study aims to evaluate the expression of plasma miR-18, thereby evaluating its potential use as a biomarker to screen acute myocardial infarction (AMI) patients from healthy controls. Methods: Real time PCR was carried out to evaluate the level of miR-18 in AMI patients and healthy controls. ROC analysis was performed to evaluate whether miR-18 could be used as a potential biomarker. Dual luciferase assay was used to identify the potential target of miR-18. Results: We showed novel data that plasma miR-18 was significantly greater in AMI patients than in healthy controls. ROC analysis indicated that plasma miR-18 could screen AMI patients from healthy controls with high sensitivity and specificity. Further study demonstrated that plasma miR-18 was positively correlated with serum cardiac troponin I (cTnI) and creatine phosphokinase-MB (CK-MB) concentrations. Additionally, plasma miR-18 was increased in AMI patients with more stenosed coronary vessels. More importantly, plasma miR-18 was decreased in AMI patients after receiving percutaneous coronary intervention (PCI). Dual luciferase reporter assay indicated that overexpression of miR-18 significantly suppressed the relative luciferase activity of pmirGLO-HIF1 alpha-3 'UTR Conclusions: In summary, enhanced plasma miR-18 could be used as a potential biomarker to screen AMI patients from healthy controls via targeting HIF1 alpha.
引用
收藏
页码:1207 / 1212
页数:6
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