Department of Respiratory and Critical Care of the Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Medicine (Baltimore). 2023 Aug 18;102(33):e34840. doi: 10.1097/MD.0000000000034840.
Acute lung injury (ALI) is an acute inflammatory disease characterized by excess production of inflammatory factors in lung tissue and has a high mortality. This research was designed for the identification of novel diagnostic biomarkers for ALI and analyzing the possible association between critical genes and infiltrated immune cells.
The study used 2 datasets (GSE2411 and GSE18341) to identify differentially expressed genes (DEGs) between 2 groups. Then we performed Gene Ontology and Kyoto Encyclopedia of Genes and Genomes analyses to identify the functions of these DEGs. The study also used SVM-recursive feature elimination analysis and least absolute shrinkage and selection operator regression model to screen possible markers. The study further analyzed immune cell infiltration via CIBERSORT. Gene Set Enrichment Analysis was used to explore the molecular mechanism of the critical genes.
DEGs were identified between 2 groups. In total, 690 DEGs were obtained: 527 genes were upregulated and 163 genes were downregulated. We identified PDZK1IP1, CCKAR, and CXCL2 as critical genes. And we then found that these critical genes correlated with Mast Cells, Neutrophil Cells, M1 Macrophage, dendritic cell Actived, Eosinophil Cells, B Cells Naive, Mast Cells, and dendritic cell Immature. Furthermore, we investigated the specific signaling pathways involved in key genes and derived some potential molecular mechanisms by which key genes affect disease progression by use of Gene Set Enrichment Analysis. Moreover, we predict transcription factors. Also, we obtained critical gene-related microRNAs through the targetscan database, and visualized the microRNA network of the genes.
Our findings might provide some novel clue for the exploration of novel markers for ALI diagnosis. The critical genes and their associations with immune infiltration may offer new insight into understanding ALI developments.
急性肺损伤(ALI)是一种以肺组织中炎症因子过度产生为特征的急性炎症性疾病,死亡率较高。本研究旨在寻找用于诊断 ALI 的新型生物标志物,并分析关键基因与浸润免疫细胞之间的可能关联。
本研究使用了 2 个数据集(GSE2411 和 GSE18341)来识别两组间差异表达基因(DEGs)。然后,我们进行了基因本体论和京都基因与基因组百科全书分析,以确定这些 DEGs 的功能。研究还使用 SVM 递归特征消除分析和最小绝对收缩和选择算子回归模型来筛选可能的标记物。研究还通过 CIBERSORT 进一步分析免疫细胞浸润。基因集富集分析用于探索关键基因的分子机制。
在两组之间鉴定出 DEGs。总共获得了 690 个 DEGs:527 个基因上调,163 个基因下调。我们鉴定出 PDZK1IP1、CCKAR 和 CXCL2 为关键基因。我们发现这些关键基因与肥大细胞、中性粒细胞、M1 巨噬细胞、激活的树突状细胞、嗜酸性粒细胞、幼稚 B 细胞、肥大细胞和不成熟的树突状细胞相关。此外,我们还通过基因集富集分析研究了关键基因所涉及的特定信号通路,并得出了一些潜在的分子机制,这些机制可能影响关键基因对疾病进展的作用。我们还预测了转录因子。此外,我们通过 targetscan 数据库获得了关键基因相关的 microRNAs,并可视化了基因的 microRNA 网络。
我们的研究结果可能为探索用于 ALI 诊断的新型生物标志物提供了一些新的线索。关键基因及其与免疫浸润的关联可能为理解 ALI 发展提供新的见解。