Clinical value of serum LncRNA EPB41L4A-AS1 in high-risk carotid artery stenosis and analysis of its mechanism

Abstract Objectives To investigate the diagnostic value of erythrocyte membrane protein band 4.1 like 4A gene antisense RNA 1 (EPB41L4A-AS1) for carotid artery stenosis (CAS) and its mechanism of action. Methods A total of 157 patients with CAS and 65 healthy individuals were included. Color doppler ultrasound determined the degree of carotid artery stenosis and plaque stability of the patients. Real-time quantitative PCR (RT-qPCR) detected the expression of EPB41L4A-AS1. Receiver operating characteristic (ROC) curve assessed the diagnostic value of EPB41L4A-AS1 for CAS. Cell counting kit-8 (CCK-8) observed the proliferative ability of the cells, Transwell detected the migration, and enzyme-linked immunoassay (ELISA) validated the expression of inflammatory factors. Results Blood pressure and low-density lipoprotein cholesterol (LDL-C) indexes were significantly elevated in CAS patients, and EPB41L4A-AS1 was significantly down-regulated, which was more pronounced in patients with heavy and unstable plaques. EPB41L4A-AS1 has diagnostic significance for the degree of carotid stenosis and plaque stability in CAS patients. Oxidized low-density lipoprotein (ox-LDL) induced cell proliferation and migration, and promotes inflammatory levels. However, overexpression of EPB41L4A-AS1 inhibited cell function and downregulated inflammatory levels. Conclusions Low EPB41L4A-AS1 was positively associated with the degree of carotid artery stenosis and plaque vulnerability in patients with CAS. Overexpression of EPB41L4A-AS1 may alleviate the degree of CAS by downregulating the expression of inflammatory factors.

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Journal
Turkish Journal of Biochemistry
Published
2025-09-08
DOI
https://doi.org/10.1515/tjb-2025-0086
Primary Topic
Cancer-related molecular mechanisms research
Type
article
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article

Clinical value of serum LncRNA EPB41L4A-AS1 in high-risk carotid artery stenosis and analysis of its mechanism

B. Li, Yan Gao, Yufeng He, Pengfei Li et al.
Turkish Journal of Biochemistry
Cancer-related molecular mechanisms research
article

Clinical value of serum LncRNA EPB41L4A-AS1 in high-risk carotid artery stenosis and analysis of its mechanism

B. Li, Yan Gao, Yufeng He, Pengfei Li, Lin Zhao, Changjing Wu, Huhe Bateer
article en

Abstract

Abstract Objectives To investigate the diagnostic value of erythrocyte membrane protein band 4.1 like 4A gene antisense RNA 1 (EPB41L4A-AS1) for carotid artery stenosis (CAS) and its mechanism of action. Methods A total of 157 patients with CAS and 65 healthy individuals were included. Color doppler ultrasound determined the degree of carotid artery stenosis and plaque stability of the patients. Real-time quantitative PCR (RT-qPCR) detected the expression of EPB41L4A-AS1. Receiver operating characteristic (ROC) curve assessed the diagnostic value of EPB41L4A-AS1 for CAS. Cell counting kit-8 (CCK-8) observed the proliferative ability of the cells, Transwell detected the migration, and enzyme-linked immunoassay (ELISA) validated the expression of inflammatory factors. Results Blood pressure and low-density lipoprotein cholesterol (LDL-C) indexes were significantly elevated in CAS patients, and EPB41L4A-AS1 was significantly down-regulated, which was more pronounced in patients with heavy and unstable plaques. EPB41L4A-AS1 has diagnostic significance for the degree of carotid stenosis and plaque stability in CAS patients. Oxidized low-density lipoprotein (ox-LDL) induced cell proliferation and migration, and promotes inflammatory levels. However, overexpression of EPB41L4A-AS1 inhibited cell function and downregulated inflammatory levels. Conclusions Low EPB41L4A-AS1 was positively associated with the degree of carotid artery stenosis and plaque vulnerability in patients with CAS. Overexpression of EPB41L4A-AS1 may alleviate the degree of CAS by downregulating the expression of inflammatory factors.

Turkish Journal of BiochemistryVol. 51(1)
Tongliao Academy of Agricultural Sciences (CN)
Openalex Percentile: Top 69%
Cancer-related molecular mechanisms research
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