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.