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Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
Circulating circ_0069094 is Correlated with the Present and Endothelial Injury of Acute Coronary Syndrome
Zhen Gao1, Peng Wu2, Hezhong Zhu3
1Department of Cardiology, Taihe Hospital, Hubei University of Medicine, No. 32, Renmin South Road, Shiyan, 442000, China.
Insights
Circ_0069094 levels decrease in acute coronary syndrome (ACS). Increasing circ_0069094 expression improves cardiac function and cell survival in ACS models by regulating miR-484.
Area of Science:
- Cardiovascular Biology
- Molecular Biology
- Biochemistry
Background:
- Acute coronary syndrome (ACS) is a major cause of mortality worldwide.
- CircRNAs are increasingly recognized for their roles in various diseases, including cardiovascular conditions.
- Understanding the specific roles of circRNAs like circ_0069094 in ACS pathogenesis is crucial for developing novel diagnostic and therapeutic strategies.
Purpose of the Study:
- To investigate the expression and functional role of circ_0069094 in acute coronary syndrome (ACS).
- To explore the diagnostic value of circ_0069094 in ACS.
- To elucidate the underlying molecular mechanism of circ_0069094 in ACS, including its interaction with miR-484.
Main Methods:
- Real-time polymerase chain reaction (RT-PCR) for circ_0069094 expression analysis.
- Receiver Operating Characteristic (ROC) curve analysis for diagnostic performance evaluation.
- Assessment of biochemical markers (SOD, MDA, vWF) and cardiac function parameters (LVIDs, LVDD, LVEF) in ACS rat models.
- Cell viability (CCK-8), migration (Transwell), and apoptosis (flow cytometry) assays in H/R HUVEC models.
- Bioinformatic analysis (GO, KEGG) to identify targeted genes of miR-484.
- Correlation analysis using Spearman's method.
Main Results:
- Circ_0069094 concentration was significantly decreased in patients with ACS, ACS rat models, and H/R HUVEC models.
- Increased circ_0069094 expression ameliorated the dysfunction of SOD, MDA, vWF, LVIDs, LVDD, and LVEF in ACS models.
- Circ_0069094 positively regulated the viability, migration, and apoptosis of H/R cell models.
- MiR-484 was identified as a competing endogenous RNA (ceRNA) of circ_0069094, mediating its functional effects.
Conclusions:
- Circ_0069094 acts as a protective factor in acute coronary syndrome.
- Circ_0069094 exhibits potential as a diagnostic biomarker for ACS.
- The circ_0069094/miR-484 axis plays a critical role in the pathogenesis and progression of ACS.
Abstract:
To investigate the impacts of circ_0069094 on acute coronary syndrome. Real-time polymerase chain reaction was used to detect the expression levels of circ_0069094, and its diagnostic performance was evaluated using ROC curve. Spearman's method was performed for correlation analysis. The levels of SOD, MDA, vWF in ACS rat models were assessed by commercial kits. The activities of H/R cell models were detected by CCK-8, Transwell, flow cytometry. The GO and KEGG were performed to analyze the function of targeted genes of miR-484. The concentration of circ_0069094 was decreased in patients with ACS, ACS rat models and H/R HUVEC models. The dysfunction of SOD, MDA, vWF, LVIDs, LVDD, and LVEF in the ACS models was regulated by the increase of circ_0069094. The viability, migration, apoptosis of the H/R models were regulated by circ_0069094. MiR-484 was a ceRNA of circ_0069094 and mediated the function of circ_0069094.
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