综合生物信息学分析表明,IRF8 是动脉粥样硬化进展过程中免疫浸润的关键生物标志物。

IF 2.9 4区 医学 Q2 Medicine Clinical and Experimental Pharmacology and Physiology Pub Date : 2024-06-17 DOI:10.1111/1440-1681.13872
Donglai Zhou, Tao Yu, Zhi Zhang, Guanhua Li, Yaomin Li
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引用次数: 0

摘要

动脉粥样硬化是一种脂质驱动的慢性炎症性疾病,是全球关注的重大健康问题,发病率和死亡率都很高,给社会造成了沉重负担。本研究的目的是调查动脉粥样硬化的可能分子机制,并确定潜在的治疗靶点。我们利用从基因表达总库(Gene Expression Omnibus)获得的外周血单核细胞和TISSUE数据库的数据进行了综合生物信息学分析,以确定与动脉粥样硬化进展相关的关键基因。研究发现,IRF8 是动脉粥样硬化患者的一个关键基因。用小干扰 RNA 抑制 IRF8 可减少内皮细胞的炎症反应。这表明IRF8是动脉粥样硬化进展过程中免疫浸润的关键生物标志物。
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An integrated bioinformatics analysis reveals IRF8 as a critical biomarker for immune infiltration in atherosclerosis advance

Atherosclerosis, a lipid-driven chronic inflammatory disorder, is a significant global health concern associated with high rates of morbidity and mortality, imposing a substantial societal burden. The purpose of this study is to investigate the possible molecular mechanisms of atherosclerosis and identify potential therapeutic targets. We conducted an integrated bioinformatics analysis using data from peripheral blood mononuclear cell and TISSUE databases obtained from the Gene Expression Omnibus, to identify key genes associated with the progression of atherosclerosis. Here, IRF8 was found to be a key gene in atherosclerosis patients. Silencing IRF8 with small interfering RNA reduced inflammation in endothelial cells. This suggests IRF8 is a crucial biomarker for immune infiltration in atherosclerosis advance.

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来源期刊
CiteScore
6.20
自引率
0.00%
发文量
128
审稿时长
6 months
期刊介绍: Clinical and Experimental Pharmacology and Physiology is an international journal founded in 1974 by Mike Rand, Austin Doyle, John Coghlan and Paul Korner. Our focus is new frontiers in physiology and pharmacology, emphasizing the translation of basic research to clinical practice. We publish original articles, invited reviews and our exciting, cutting-edge Frontiers-in-Research series’.
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