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自噬介导的表达簇参与冠心病的免疫调节。

Autophagy-mediated expression clusters are involved in immunity regulation of coronary artery disease.

机构信息

Cardiovascular Disease Center, The Central Hospital Of Enshi Tujia And Miao Autonomous Prefecture, Enshi, 445000, Hubei, China.

出版信息

BMC Genom Data. 2022 Apr 2;23(1):24. doi: 10.1186/s12863-022-01023-3.

Abstract

BACKGROUND

The association between autophagy and immunity, including infiltrating immunocytes, immune reaction gene-sets, and HLAs (human leukocyte antigen) gene, remains unclear. The present study aimed to provide a valid diagnostic tool for coronary artery disease (CAD), and explore the pathological mechanisms of CAD based on the association between autophagy and immunity.

METHODS

First, the overlap between differentially expressed genes (DEGs) and autophagy-related genes (ARGs) was identified. Subsequently, machine learning was conducted to screen risk genes closely related to CAD. Diverse autophagy phenotype-related clusters were identified using unsupervised clustering. The connections between different clusters and immune characteristics were evaluated as well.

RESULTS

The present study identified 27 differentially expressed autophagy-related genes (DEAGRs) in CAD samples compared with healthy conrtrols. A classifier constructing by 9 DEARGs was regarded as an effective diagnostic tool for CAD. Furthermore, three distinct autophagy phenotype - related clusters were identified, each cluster exhibited different immune characteristics. Finally, the gene ontology (GO) analysis of 901 autophagy phenotype-related genes showed that immune response, protein phosphorylation, and innate immune response were remarkable enrichment components.

CONCLUSIONS

This study identified an effective classifier constituted by 9-DEARGs that has good diagnostic performance for CAD, and revealed that autophagy and the immunity may be common critical factors in the occurrence and development of CAD.

摘要

背景

自噬与免疫之间的关系,包括浸润免疫细胞、免疫反应基因集和 HLA(人类白细胞抗原)基因,尚不清楚。本研究旨在为冠状动脉疾病 (CAD) 提供有效的诊断工具,并基于自噬与免疫之间的关系,探讨 CAD 的病理机制。

方法

首先,确定差异表达基因 (DEGs) 和自噬相关基因 (ARGs) 之间的重叠。然后,采用机器学习筛选与 CAD 密切相关的风险基因。使用无监督聚类识别不同的自噬表型相关聚类。评估不同聚类与免疫特征之间的关系。

结果

与健康对照组相比,本研究在 CAD 样本中鉴定出 27 个差异表达的自噬相关基因 (DEAGRs)。由 9 个 DEARGs 构建的分类器被认为是 CAD 的有效诊断工具。此外,鉴定出三种不同的自噬表型相关聚类,每个聚类表现出不同的免疫特征。最后,对 901 个自噬表型相关基因的基因本体 (GO) 分析表明,免疫反应、蛋白磷酸化和固有免疫反应是显著富集的成分。

结论

本研究确定了一个由 9 个 DEARGs 组成的有效分类器,对 CAD 具有良好的诊断性能,并揭示了自噬和免疫可能是 CAD 发生和发展的共同关键因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb77/8976398/bda3ddb1a9a2/12863_2022_1023_Fig1_HTML.jpg

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