LncRNA LUCAT1 offers protection against human coronary artery endothelial cellular oxidative stress injury through modulating hsa-miR-6776-5p/LRRC25 axis and activating autophagy flux

Our results delineated the dynamic disruption of the autophagy landscape during the progression of human coronary atherosclerosis and identified the lncRNA LUCAT1/hsa-miR-6776-5p/LRRC25 axis, uncovered through transcriptomic profiling, as a protective mechanism against endothelial cell injury through autophagy activation. Furthermore, we recognized p62, ATG7, lncRNA LUCAT1, and LRRC25 as dependable autophagy-related diagnostic biomarkers in circulating PBMCs, correlating with CAD severity. Collectively, Our findings furnish novel insights into the intricate autophagy landscape at various levels of coronary atherosclerosis and propose potential diagnostic biomarkers, and a theoretical foundation for managing CAD patients.

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Publication Details

Journal
Journal of Translational Medicine
Published
2024-12-31
DOI
https://doi.org/10.1186/s12967-024-05966-2
Citations
4
Primary Topic
Cancer-related molecular mechanisms research
Type
article
Field-Weighted Citation Impact
1.14

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article

LncRNA LUCAT1 offers protection against human coronary artery endothelial cellular oxidative stress injury through modulating hsa-miR-6776-5p/LRRC25 axis and activating autophagy flux

Boyu Chi, Qiaowei Jia, En‐Zhi Jia, Fenghui An et al.
4 citations
Journal of Translational Medicine
Cancer-related molecular mechanisms research
1.14
article

LncRNA LUCAT1 offers protection against human coronary artery endothelial cellular oxidative stress injury through modulating hsa-miR-6776-5p/LRRC25 axis and activating autophagy flux

Boyu Chi, Qiaowei Jia, En‐Zhi Jia, Fenghui An, Xiongkang Gan, Yahong Fu, Chengcheng Li, Yanjun Wang, Sheng Zhang, Zhiyuan Chen, Mengmeng Ren, Shu He, Xiumei Chen, Hanxiao Zhou, Hengjie Bie, M Duan, Xin Zhang, Qian Zhang
article en
4 citations

Abstract

Our results delineated the dynamic disruption of the autophagy landscape during the progression of human coronary atherosclerosis and identified the lncRNA LUCAT1/hsa-miR-6776-5p/LRRC25 axis, uncovered through transcriptomic profiling, as a protective mechanism against endothelial cell injury through autophagy activation. Furthermore, we recognized p62, ATG7, lncRNA LUCAT1, and LRRC25 as dependable autophagy-related diagnostic biomarkers in circulating PBMCs, correlating with CAD severity. Collectively, Our findings furnish novel insights into the intricate autophagy landscape at various levels of coronary atherosclerosis and propose potential diagnostic biomarkers, and a theoretical foundation for managing CAD patients.

Journal of Translational MedicineVol. 22(1)
Yili Friendship Hospital (CN), Jiangsu Province Hospital (CN), Nanjing Medical University (CN)
National Natural Science Foundation of China, Government of Jiangsu Province, Nanjing Medical University, Priority Academic Program Development of Jiangsu Higher Education Institutions, Collaborative Innovation Center for Cardiovascular Disease Translational Medicine
Good health and well-being
Openalex Percentile: Top 20%
Cancer-related molecular mechanisms research
1.14
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