Department of Thoracic Surgery, Tangshan People's Hospital, Hebei, P.R. China.
Department of Breast Surgery, Tangshan People's Hospital, Hebei, P.R. China.
Gen Physiol Biophys. 2023 Nov;42(6):479-493. doi: 10.4149/gpb_2023025.
This study aimed to identify glycosylation-related genes associated with lung adenocarcinoma (LUAD) prognosis through comprehensive bioinformatic analysis. Glycosylation-related genes were identified from the Human Gene Nomenclature Committee, and LUAD prognostic genes were screened from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO)-GSE68465 datasets. Glycosylation risk score (GLRS) was calculated to predict LUAD prognostic risk. Samples were grouped into GLRS-high and GLRS-low and compared. The Tumor Immune Dysfunction and Exclusion (TIDE) score was computed to assess the antitumor immune escape possibility after immunotherapy. From 213 glycosylation-related genes, five gene signatures served as prognostic LUAD predictors using univariate and stepwise Cox regression analyses. GLRS-based models were constructed using TCGA and GSE68465 samples; their sensitivity and specificity in predicting LUAD prognosis were confirmed. GLRS was an independent LUAD prognostic factor and contributed to the nomogram to predict patient survival. High GLRS was associated with advanced tumor stage and higher mutation frequencies, estimate scores, and TIDE scores. GLRS-high and GLRS-low patients differed in immune cell infiltration and epithelial-mesenchymal transition (EMT)-related gene expression. Thus, we propose five glycosylation-related gene signatures to predict overall survival and prognostic risks of LUAD. Their regulatory roles may be related to immune invasion, immunotherapy response, mutation, and EMT.
本研究旨在通过综合生物信息学分析,确定与肺腺癌(LUAD)预后相关的糖基化相关基因。从人类基因命名委员会中鉴定糖基化相关基因,并从癌症基因组图谱(TCGA)和基因表达综合数据库(GEO)-GSE68465 数据集筛选 LUAD 预后基因。计算糖基化风险评分(GLRS)以预测 LUAD 预后风险。将样本分为 GLRS 高和 GLRS 低两组进行比较。计算肿瘤免疫功能障碍和排除(TIDE)评分,以评估免疫治疗后抗肿瘤免疫逃逸的可能性。从 213 个糖基化相关基因中,使用单变量和逐步 Cox 回归分析,筛选出 5 个基因特征作为 LUAD 预后预测标志物。使用 TCGA 和 GSE68465 样本构建基于 GLRS 的模型,验证其预测 LUAD 预后的敏感性和特异性。GLRS 是 LUAD 的独立预后因素,并有助于预测患者生存的列线图的构建。高 GLRS 与肿瘤晚期、更高的突变频率、估计评分和 TIDE 评分相关。GLRS 高和 GLRS 低患者的免疫细胞浸润和上皮-间充质转化(EMT)相关基因表达存在差异。因此,我们提出了 5 个糖基化相关基因特征来预测 LUAD 的总生存期和预后风险。它们的调控作用可能与免疫浸润、免疫治疗反应、突变和 EMT 有关。