Events1st International Electronic Conference on Biomedicine
Published
This submission belongs to the session S9. Translational Biomarkers in Clinical Biomedicine and Precision Medicine of the event 1st International Electronic Conference on Biomedicine
Published date
01 Jun, 2021
Citation
Byeong Hwa Jeon, Hee Kyoung Joo, Yu Ran Lee, Eun-Ok Lee, Serologic APE1/Ref-1: New biomarker for Vascular Inflammation in Atherosclerosis., in Proceedings of 1st International Electronic Conference on Biomedicine, 1 June–26 June 2021, MDPI: Basel, Switzerland, doi: 10.3390/ECB2021-10289
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Serologic APE1/Ref-1: New biomarker for Vascular Inflammation in Atherosclerosis.

Eun-Ok Lee 1
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1. Chungnam National University
2. Chungnam National University, South Korea
Abstract

Apurinic/apyrimidinic endonuclease 1/redox factor-1 (APE1/Ref-1) is a secretable multifunctional protein. Since the concept of APE1/Ref-1 secretion was established in 2013, several studies have demonstrated the usefulness of APE1/Ref-1 as a serological biomarker. However, the role of APE1/Ref-1 in atherosclerotic vascular inflammation is unclear. Herein, we investigated the role of APE1/Ref-1 in atherosclerotic apolipoprotein E (ApoE-/-) mice fed with a Western-type diet as an animal model of vascular inflammation. We found that serologic APE1/Ref-1 was strongly correlated with vascular inflammation in these mice. Neutrophil/lymphocyte ratio, endothelial cell/macrophage activation, and atherosclerotic plaque formation, reflected by atherosclerotic inflammation, were increased in the ApoE-/- mice fed with a Western-type diet. Correlation analysis showed a high correlation between plasma APE1/Ref-1 levels and neutrophil/lymphocyte ratio, a marker of systemic inflammation. We conclude that APE1/Ref-1 expression is upregulated in aortic endothelial cells/macrophages of atherosclerotic mice, and that plasma APE1/Ref-1 levels could predict atherosclerotic inflammation, it is a useful biomarker for vascular inflammation in atherosclerosis.

Keywords
APE1/Ref-1
vascular inflammation
biomarker
ApoE KO mice
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