Faculty of Pharmacy, Guangxi Agricultural Vocational and Technical University, Nanning 530007, China; Faculty of Pharmacy, Guangxi University of Chinese Medicine, Nanning 530022, China.
Guangxi International Zhuang Medical Hospital, Nanning 530003, China.
Gene. 2023 Feb 5;852:147032. doi: 10.1016/j.gene.2022.147032. Epub 2022 Nov 17.
Gastric cancer (GC) is a common primary stomach tumor of the central nervous system with a poor prognosis. In this study, 274 differentially expressed immune-related genes (DEIRGs) were identified among six cell subpopulations in GSE112302 single-cell RNA sequencing (scRNA-seq) data of GC. Those DEIRGs were able to divide GC patients into three distinct subtypes with different overall survivals and tumor microenvironment. By univariate Cox and LASSO regression analyses, eight immune-related genes, including CTGF, CXCL3, CXCR4, NRP1, OAS1, SP1, STC1 and TAP1, were identified as GC prognostic signatures. Accordingly, a risk score model for predicting GC prognosis was constructed in TCGA-GC training cohort and validated in the external GSE66229 dataset. Moreover, a nomogram for predicting the survival of GC patients was also established based on independent prognostic factors (age, grade, cancer status and risk score) identified by univariate and multivariate Cox regression analyses. In addition, Gene Set Variation Analysis (GSVA) analysis indicated that the prognostic immune signatures may regulate GC via inflammation and cell proliferation related pathways, such as DNA replication, complement and coagulation cascades, focal adhesion and TGF-β signaling pathway.
胃癌(GC)是一种常见的中枢神经系统原发性胃肿瘤,预后不良。在这项研究中,我们从 GSE112302 单细胞 RNA 测序(scRNA-seq)数据的 GC 的六个细胞亚群中鉴定出了 274 个差异表达的免疫相关基因(DEIRGs)。这些 DEIRGs 能够将 GC 患者分为三种不同的亚型,具有不同的总体生存率和肿瘤微环境。通过单因素 Cox 和 LASSO 回归分析,我们鉴定出了 8 个免疫相关基因,包括 CTGF、CXCL3、CXCR4、NRP1、OAS1、SP1、STC1 和 TAP1,作为 GC 的预后特征。相应地,我们在 TCGA-GC 训练队列中构建了预测 GC 预后的风险评分模型,并在外部 GSE66229 数据集进行了验证。此外,我们还基于单因素和多因素 Cox 回归分析确定的独立预后因素(年龄、分级、癌症状态和风险评分),建立了预测 GC 患者生存的列线图。此外,基因集变异分析(GSVA)分析表明,这些预后免疫特征可能通过炎症和细胞增殖相关途径(如 DNA 复制、补体和凝血级联、黏附和 TGF-β 信号通路)调节 GC。