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Updated: Dec 13, 2025

Digital PCR for Quantifying Circulating MicroRNAs in Acute Myocardial Infarction and Cardiovascular Disease
Published on: July 3, 2018
MicroRNA microarray analysis to detect biomarkers of aortic dissection from paraffin-embedded tissue samples
1Department of Cardiovascular Surgery, University of Chinese Academy of Sciences Shenzhen Hospital, Shenzhen, China.
MicroRNA-636 is significantly elevated in acute aortic dissection (AAD) tissues. This finding suggests microRNA-636 may serve as a novel biomarker for diagnosing AAD.
Area of Science:
- Molecular Biology
- Cardiovascular Research
- Biomarker Discovery
Background:
- Acute aortic dissection (AAD) is a life-threatening condition requiring improved diagnostic tools.
- MicroRNAs (miRNAs) are small non-coding RNAs with roles in various biological processes, including cardiovascular diseases.
Purpose of the Study:
- To investigate differential microRNA expression profiles in acute aortic dissection (AAD) tissues.
- To identify potential microRNA biomarkers for AAD diagnosis and pathogenesis.
Main Methods:
- MicroRNA microarray analysis of 92 paraffin-embedded AAD tissues and 54 control aortic segments.
- Validation of differentially expressed miRNAs using real-time fluorescence quantitative polymerase chain reaction (RT-qPCR) and fluorescence in situ hybridization (FISH).
Main Results:
- 71 differentially expressed miRNAs were identified between AAD and control groups.
- Hsa-miR-636 was significantly up-regulated in AAD tissues (3.3-fold by RT-qPCR, P=0.012).
- FISH confirmed significantly increased hsa-miR-636 expression in AAD tissues (P<0.001).
Conclusions:
- Hsa-miR-636 is implicated in the pathogenesis of acute aortic dissection.
- Hsa-miR-636 shows potential as a diagnostic biomarker for AAD.
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