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生物信息学和系统生物学方法揭示新型冠状病毒肺炎与非酒精性肝炎之间的共享基因和分子机制。

Bioinformatic and systems biology approach revealing the shared genes and molecular mechanisms between COVID-19 and non-alcoholic hepatitis.

作者信息

Lu Huishuang, Ma Jiaxiu, Li Yalan, Zhang Jin, An Yaxin, Du Wei, Cai Xuefei

机构信息

The Key Laboratory of Molecular Biology of Infectious Diseases Designated by the Chinese Ministry of Education, Chongqing Medical University, Chongqing, China.

出版信息

Front Mol Biosci. 2023 Jun 19;10:1164220. doi: 10.3389/fmolb.2023.1164220. eCollection 2023.

Abstract

Coronavirus disease 2019 (COVID-19) has become a global pandemic and poses a serious threat to human health. Many studies have shown that pre-existing nonalcoholic steatohepatitis (NASH) can worsen the clinical symptoms in patients suffering from COVID-19. However, the potential molecular mechanisms between NASH and COVID-19 remain unclear. To this end, key molecules and pathways between COVID-19 and NASH were herein explored by bioinformatic analysis. The common differentially expressed genes (DEGs) between NASH and COVID-19 were obtained by differential gene analysis. Enrichment analysis and protein-protein interaction (PPI) network analysis were carried out using the obtained common DEGs. The key modules and hub genes in PPI network were obtained by using the plug-in of Cytoscape software. Subsequently, the hub genes were verified using datasets of NASH (GSE180882) and COVID-19 (GSE150316), and further evaluated by principal component analysis (PCA) and receiver operating characteristic (ROC). Finally, the verified hub genes were analyzed by single-sample gene set enrichment analysis (ssGSEA) and NetworkAnalyst was used for the analysis of transcription factor (TF)-gene interactions, TF-microRNAs (miRNA) coregulatory network, and Protein-chemical Interactions. A total of 120 DEGs between NASH and COVID-19 datasets were obtained, and the PPI network was constructed. Two key modules were obtained via the PPI network, and enrichment analysis of the key modules revealed the common association between NASH and COVID-19. In total, 16 hub genes were obtained by five algorithms, and six of them, namely, Kruppel-like factor 6 (KLF6), early growth response 1 (EGR1), growth arrest and DNA-damage-inducible 45 beta (GADD45B), JUNB, FOS, and FOS-like antigen 1 (FOSL1) were confirmed to be closely related to NASH and COVID-19. Finally, the relationship between hub genes and related pathways was analyzed, and the interaction network of six hub genes was constructed with TFs, miRNAs, and compounds. This study identified six hub genes related to COVID-19 and NASH, providing a new perspective for disease diagnosis and drug development.

摘要

2019冠状病毒病(COVID-19)已成为全球大流行疾病,对人类健康构成严重威胁。许多研究表明,既往存在的非酒精性脂肪性肝炎(NASH)会使COVID-19患者的临床症状恶化。然而,NASH与COVID-19之间潜在的分子机制仍不清楚。为此,本文通过生物信息学分析探索了COVID-19与NASH之间的关键分子和通路。通过差异基因分析获得了NASH与COVID-19之间的共同差异表达基因(DEG)。利用获得的共同DEG进行富集分析和蛋白质-蛋白质相互作用(PPI)网络分析。使用Cytoscape软件插件获得PPI网络中的关键模块和枢纽基因。随后,利用NASH(GSE180882)和COVID-19(GSE150316)数据集对枢纽基因进行验证,并通过主成分分析(PCA)和受试者工作特征(ROC)进一步评估。最后,通过单样本基因集富集分析(ssGSEA)对验证后的枢纽基因进行分析,并使用NetworkAnalyst对转录因子(TF)-基因相互作用、TF-微小RNA(miRNA)共调控网络和蛋白质-化学相互作用进行分析。在NASH与COVID-19数据集之间共获得120个DEG,并构建了PPI网络。通过PPI网络获得了两个关键模块,对关键模块的富集分析揭示了NASH与COVID-19之间的共同关联。通过五种算法共获得16个枢纽基因,其中6个,即 Kruppel样因子6(KLF6)、早期生长反应1(EGR1)、生长停滞和DNA损伤诱导45β(GADD45B)、JUNB、FOS和FOS样抗原1(FOSL1)被证实与NASH和COVID-19密切相关。最后,分析了枢纽基因与相关通路之间的关系,并用TF、miRNA和化合物构建了6个枢纽基因的相互作用网络。本研究鉴定了6个与COVID-19和NASH相关的枢纽基因,为疾病诊断和药物开发提供了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9fb1/10315682/78c894376610/fmolb-10-1164220-g001.jpg

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