1.MiR-34a, miR-21 and miR-23a as potential biomarkers for coronary artery disease: a pilot microarray study and confirmation in a 32 patient cohort.
Hui HAN ; Guangjin QU ; Chenghua HAN ; Yuhong WANG ; Tingting SUN ; Fengqing LI ; Junxiao WANG ; Shanshun LUO
Experimental & Molecular Medicine 2015;47(2):e138-
The aim of this study was to investigate the expression of circulating microRNAs (miRNAs) in apolipoprotein E (apoE) knockout mice (apoE-/-) and to validate the role of these miRNAs in human coronary artery disease (CAD). Pooled plasma from 10 apoE-/- mice and 10 healthy C57BL/6 (B6) mice was used to perform the microarray analysis. The results showed that miR-34a, miR-21, miR-23a, miR-30a and miR-106b were differentially expressed in apoE-/- mice, and these expression changes were confirmed by real-time quantitative reverse-transcription PCR. Then, miR-34a, miR-21, miR-23a, miR-30a and miR-106b were detected in the plasma of 32 patients with CAD and of 20 healthy controls. Only miR-34a, miR-21 and miR-23a were significantly differentially expressed in the plasma of CAD patients (all P<0.01). In conclusion, miR-34a, miR-21 and miR-23a were elevated in CAD patients, which means that these miRNAs might serve as biomarkers of CAD development and progression.
Aged
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Animals
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Apolipoproteins E/deficiency
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Biomarkers
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Case-Control Studies
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Coronary Artery Disease/*genetics
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Disease Models, Animal
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Gene Expression Profiling
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Gene Expression Regulation
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Humans
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Male
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Mice
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Mice, Knockout
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MicroRNAs/*genetics
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Middle Aged
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Pilot Projects
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Reproducibility of Results
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Risk Factors