Sun Zhongyi, Hu Yanan, Qu Jiachen, Zhao Qiuyue, Gao Han, Peng Zhiyong
Department of Critical Care Medicine, Zhongnan Hospital of Wuhan University, Wuhan, China.
Clinical Research Center of Hubei Critical Care Medicine, Wuhan, China.
Front Genet. 2024 Jun 4;15:1389630. doi: 10.3389/fgene.2024.1389630. eCollection 2024.
Sepsis leads to multi-organ dysfunction due to disorders of the host response to infections, which makes diagnosis and prognosis challenging. Apoptosis, a classic programmed cell death, contributes to the pathogenesis of various diseases. However, there is much uncertainty about its mechanism in sepsis.
Three sepsis gene expression profiles (GSE65682, GSE13904, and GSE26378) were downloaded from the Gene Expression Omnibus database. Apoptosis-related genes were obtained from the Kyoto Encyclopedia of Genes and Genomes Pathway database. We utilized LASSO regression and SVM-RFE algorithms to identify characteristic genes associated with sepsis. CIBERSORT and single cell sequencing analysis were employed to explore the potential relationship between hub genes and immune cell infiltration. The diagnostic capability of hub genes was validated across multiple external datasets. Subsequently, the animal sepsis model was established to assess the expression levels of hub genes in distinct target organs through RT-qPCR and Immunohistochemistry analysis.
We identified 11 apoptosis-related genes as characteristic diagnostic markers for sepsis: , , , , , , , , , , and . Subsequently, a prognostic model was constructed using LASSO regression with , , and identified as hub genes. Apoptosis-related genes were closely associated with the immune response during the sepsis process. Furthermore, in the validation datasets, aside from , other hub genes demonstrated similar expression patterns and diagnostic abilities as observed in GSE65682 dataset. In the mouse model, the expression differences of hub genes between sepsis and control group revealed the potential impacts on sepsis-induced organ injury.
The current findings indicated the participant of apoptosis in sepsis, and apoptosis-related differentially expressed genes could be used for diagnosis biomarkers. , , and might be key regulatory genes affecting apoptosis in sepsis. Our findings provided a novel aspect for further exploration of the pathological mechanisms in sepsis.
脓毒症由于宿主对感染的反应紊乱而导致多器官功能障碍,这使得诊断和预后具有挑战性。细胞凋亡是一种经典的程序性细胞死亡,参与多种疾病的发病机制。然而,其在脓毒症中的机制仍存在诸多不确定性。
从基因表达综合数据库下载了三个脓毒症基因表达谱(GSE65682、GSE13904和GSE26378)。从京都基因与基因组百科全书通路数据库中获取细胞凋亡相关基因。我们利用LASSO回归和支持向量机递归特征消除算法来识别与脓毒症相关的特征基因。采用CIBERSORT和单细胞测序分析来探讨枢纽基因与免疫细胞浸润之间的潜在关系。在多个外部数据集中验证了枢纽基因的诊断能力。随后,建立动物脓毒症模型,通过实时定量聚合酶链反应和免疫组织化学分析评估枢纽基因在不同靶器官中的表达水平。
我们鉴定出11个细胞凋亡相关基因作为脓毒症的特征性诊断标志物: , , , , , , , , , , 和 。随后,使用LASSO回归构建了一个预后模型,其中 , , 和 被确定为枢纽基因。细胞凋亡相关基因与脓毒症过程中的免疫反应密切相关。此外,在验证数据集中,除了 之外,其他枢纽基因表现出与GSE65682数据集中观察到的相似表达模式和诊断能力。在小鼠模型中,脓毒症组和对照组之间枢纽基因表达差异揭示了其对脓毒症诱导的器官损伤的潜在影响。
目前的研究结果表明细胞凋亡参与了脓毒症,且细胞凋亡相关差异表达基因可作为诊断生物标志物。 , , 和 可能是影响脓毒症中细胞凋亡的关键调控基因。我们的研究结果为进一步探索脓毒症的病理机制提供了一个新的视角。