Author:
Lai Zhichao,Wang Chaonan,Liu Xiaoyan,Sun Haidan,Guo Zhengguang,Shao Jiang,Li Kang,Chen Junye,Wang Jiaxian,Lei Xiangling,Shu Keqiang,Feng Yuyao,Kong Deqiang,Sun Wei,Liu Bao
Abstract
Abstract
Background
Currently, noninvasive imaging techniques and circulating biomarkers are still insufficient to accurately assess carotid plaque stability, and an in-depth understanding of the molecular mechanisms that contribute to plaque instability is still lacking.
Methods
We established a clinical study cohort containing 182 patients with carotid artery stenosis. After screening, 39 stable and 49 unstable plaques were included in the discovery group, and quantitative proteomics analysis based on data independent acquisition was performed for these plaque samples. Additionally, 35 plaques were included in the validation group to validate the proteomics results by immunohistochemistry analysis.
Results
A total of 397 differentially expressed proteins were identified in stable and unstable plaques. These proteins are primarily involved in ferroptosis and lipid metabolism-related functions and pathways. Plaque validation results showed that ferroptosis- and lipid metabolism-related proteins had different expression trends in stable plaques versus unstable fibrous cap regions and lipid core regions. Ferroptosis- and lipid metabolism-related mechanisms in plaque stability were discussed.
Conclusions
Our results may provide a valuable strategy for revealing the mechanisms affecting plaque stability and will facilitate the discovery of specific biomarkers to broaden the therapeutic scope.
Funder
National Natural Science Foundation of China
National High Level Hospital Clinical Research Funding
CAMS Innovation Fund for Medical Sciences
Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences
Fundamental Research Funds for the Central Universities
Beijing Medical Research
Publisher
Springer Science and Business Media LLC
Cited by
1 articles.
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