Zhang Sheng, Lin Kun, Qiu Jun, Feng Bin, Wang Juan, Li Jia, Peng Xia, Ji Renxin, Qiao Longwei, Liang Yuting
Center for Clinical Laboratory, The First Affiliated Hospital of Soochow University Suzhou 215006, Jiangsu, China.
Department of Laboratory Medicine, The Affiliated Hospital of Putian University Putian 351100, Fujian, China.
Am J Transl Res. 2022 Oct 15;14(10):7350-7361. eCollection 2022.
Asthma is a chronic respiratory disease characterized by airway remodeling and inflammation. Recent studies have demonstrated that multiple autophagy-related genes are involved in the pathogenesis of asthma. However, the roles of many of these autophagy-related genes in asthma remain unclear, particularly with regard to the diagnosis of asthma.
In this study, autophagy-related differentially expressed genes (DEGs) in asthma were identified by bioinformatics analysis of the GSE76262 datasets. Hub genes were screened by protein-protein interaction (PPI) network and module analyses. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analyses were used to explore potential signaling pathways. Receiver operating characteristic (ROC) curve analysis was performed to evaluate the diagnostic value of autophagy-related biomarkers in asthma.
A total of 17 autophagy-related DEGs were identified, most of which were involved in autophagy and protein processing in the endoplasmic reticulum signaling pathway. ROC curve analysis demonstrated that the hub genes (, and ) identified from the PPI network exhibited good performance in the diagnosis of asthma. The GSE137268 and GSE43696 databases were used to verify the expression of 17 autophagy-related DEGs in asthma. Interestingly, was an overlapping gene defined by the intersection of hub autophagy-related DEGs and key modules (including , and ). We also analyzed the interaction between miRNAs and mRNAs for 14 autophagy-related DEGs with an area under the curve > 0.7. The identified genes were involved in the glypican, interferon-gamma, and plasma membrane estrogen receptor signaling pathways.
The results of this study indicate that specific signaling pathways and autophagy-related DEGs are potential diagnostic biomarkers related to the inception and progression of asthma.
哮喘是一种以气道重塑和炎症为特征的慢性呼吸道疾病。最近的研究表明,多个自噬相关基因参与哮喘的发病机制。然而,这些自噬相关基因中许多在哮喘中的作用仍不清楚,特别是在哮喘诊断方面。
在本研究中,通过对GSE76262数据集进行生物信息学分析,鉴定哮喘中自噬相关差异表达基因(DEGs)。通过蛋白质-蛋白质相互作用(PPI)网络和模块分析筛选枢纽基因。利用基因本体论和京都基因与基因组百科全书通路富集分析来探索潜在的信号通路。进行受试者工作特征(ROC)曲线分析以评估自噬相关生物标志物在哮喘诊断中的价值。
共鉴定出17个自噬相关DEGs,其中大部分参与内质网信号通路中的自噬和蛋白质加工。ROC曲线分析表明,从PPI网络中鉴定出的枢纽基因(、和)在哮喘诊断中表现良好。利用GSE137268和GSE43696数据库验证17个自噬相关DEGs在哮喘中的表达。有趣的是,是由枢纽自噬相关DEGs与关键模块(包括、和)的交集定义的重叠基因。我们还分析了曲线下面积>0.7的14个自噬相关DEGs的miRNA与mRNA之间的相互作用。鉴定出的基因参与了磷脂酰肌醇蛋白聚糖、干扰素-γ和质膜雌激素受体信号通路。
本研究结果表明,特定的信号通路和自噬相关DEGs是与哮喘发生和发展相关的潜在诊断生物标志物。