A novel basement membrane-related gene signature for prognosis of lung adenocarcinomas

比例危险模型 腺癌 肿瘤科 基因 免疫系统 内科学 单变量 生存分析 多元统计 肺癌 多元分析 生物 单变量分析 医学 免疫学 癌症 遗传学 计算机科学 机器学习
作者
Zhenxing Zhang,Haoran Zhu,Xiaojun Wang,Shanan Lin,Chenjin Ruan,Qiang Wang
出处
期刊:Computers in Biology and Medicine [Elsevier BV]
卷期号:154: 106597-106597 被引量:27
标识
DOI:10.1016/j.compbiomed.2023.106597
摘要

Lung adenocarcinoma (LUAD) remains a global health concern with its poor prognosis and high mortality. Whether tumor cells invade through the basement membrane (BM) is the key factor to determine the prognosis of LUAD. This study aimed to identify the BM-related gene signatures to improve the overall prognosis of LUAD.A series of bioinformatics analyses were conducted based on TCGA and GEO datasets. Unsupervised consistent cluster analysis was performed, and 500 LUAD patients were assigned to two different groups according to expressions of 222 BM-related genes. The differentially expressed genes (DEGs) between the two clusters were identified, and Lasso regression, ROC curve, univariate and multivariate Cox regression analyses and enrichment analysis were conducted. Besides, ssGSEA, CIBERSORT and ESTIMATE algorithmwere were employed to understand the relationship between the tumor microenvironment (TME) and risk scores. Moreover, single cell clustering and trajectory analyses were performed to further understand the significance of BM-related genes. Finally, qRT-PCR was used to verify the prognosis model.A total of 31 prognostic BM-related genes were determined for LUAD, and a novel 17-mRNA prognostic model named BMsocre was successfully established to predict the overall survival of LUAD patients. The high BMscore group indicated worse prognosis. Seventeen DEGs were enriched mainly in metabolism, ECM-receptor interaction and immune response. In addition, the high-risk group showed higher TMB and lower immune score. The low-risk group had a better immunotherapeutic response where immune escape was less likely. The BMscore model was verified in our patient cohort. Furthermore, NELL2 was mainly expressed in clusters of T cells, and was identified to play a critical role in T-cell differentiation.A novel BMscore model was successfully established and might be effective for providing guidance to LUAD therapy.
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