microRNA-3646 serves as a diagnostic marker and mediates the inflammatory response induced by acute coronary syndrome

Bioengineered. 2021 Dec;12(1):5632-5640. doi: 10.1080/21655979.2021.1967066.

Abstract

Acute coronary syndrome (ACS) is one of the main syndromes of coronary artery disease with high mortality. The identification of biomarkers associated with disease occurrence and progression could improve early detection and risk prediction. This study was aimed to reveal the clinical significance and function of miR-3646 in ACS.The expression of miR-3646 was evaluated in ACS patients, healthy volunteers, and non-ACS patients and estimated the clinical significance of miR-3646. The ACS modeling rats were also established in this study to explore the potential mechanism underlying the function of miR-3646. miR-3646 was upregulated in ACS patients compared with healthy volunteers and non-ACS patients. The expression of miR-3646 was positively correlated with the severity and progression of ACS patients and could discriminate ACS patients from healthy volunteers and non-ACS patients. The knockdown of miR-3646 could reverse the inflammatory response induced by ACS.miR-3646 serves as a diagnostic biomarker for ACS. The knockdown of miR-3646 could alleviate ACS by reversing inflammatory response. These results provide a potential therapeutic target of ACS.

Keywords: acute coronary syndrome; inflammatory response; miR-3646.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Coronary Syndrome* / genetics
  • Acute Coronary Syndrome* / immunology
  • Acute Coronary Syndrome* / metabolism
  • Aged
  • Animals
  • Biomarkers / metabolism
  • Female
  • Humans
  • Inflammation / genetics
  • Inflammation / immunology
  • Inflammation / metabolism
  • Male
  • MicroRNAs* / genetics
  • MicroRNAs* / immunology
  • MicroRNAs* / metabolism
  • Middle Aged
  • Rats
  • Rats, Sprague-Dawley
  • Up-Regulation

Substances

  • Biomarkers
  • MIRN3646 microRNA, human
  • MicroRNAs

Grants and funding

This study was funded by Zibo City Key Research and Development Program Project Description(2019ZC060015).