The prognostic value of bioinformatics analysis of ECM receptor signaling pathways and LAMB1 identification as a promising prognostic biomarker of lung adenocarcinoma

被引:1
作者
Liu, Tingjun [1 ]
Liu, Jing [2 ]
Chen, Quangang [1 ]
Wu, Lianlian [1 ]
Zhang, Lingzhi [1 ]
Qiao, Dandan [1 ]
Huang, Zhutao [1 ]
Lu, Tianyuan [1 ]
Hu, Ankang [1 ]
Wang, Jie [1 ]
机构
[1] Xuzhou Med Univ, Ctr Anim Lab, Xuzhou 221009, Jiangsu, Peoples R China
[2] Xuzhou Cent Hosp, Dept Resp Med, Xuzhou, Jiangsu, Peoples R China
关键词
extracellular matrix receptor interaction; lung adenocarcinoma; prognostic model; tumor immune microenvironment; EXTRACELLULAR-MATRIX; CANCER CELLS;
D O I
10.1097/MD.0000000000039854
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The extracellular matrix (ECM) is a complex and dynamic network of cross-linked proteins and a fundamental building block in multicellular organisms. Our study investigates the impact of genes related to the ECM receptor interaction pathway on immune-targeted therapy and lung adenocarcinoma (LUAD) prognosis. This study obtained LUAD chip data (GSE68465, GSE31210, and GSE116959) from NCBI GEO. Moreover, the gene data associated with the ECM receptor interaction pathway was downloaded from the Molecular Signature Database. Differentially expressed genes were identified using GEO2R, followed by analyzing their correlation with immune cell infiltration. Univariate Cox regression analysis screened out ECM-related genes significantly related to the survival prognosis of LUAD patients. Additionally, Lasso regression and multivariate Cox regression analysis helped construct a prognostic model. Patients were stratified by risk score and survival analyses. The prognostic models were evaluated using receiver operating characteristic curves, and risk scores and prognosis associations were analyzed using univariate and multivariate Cox regression analyses. A core gene was selected for gene set enrichment analysis and CIBERSORT analysis to determine its function and tumor-infiltrating immune cell proportion, respectively. The results revealed that the most abundant pathways among differentially expressed genes in LUAD primarily involved the cell cycle, ECM receptor interaction, protein digestion and absorption, p53 signaling pathway, complement and coagulation cascade, and tyrosine metabolism. Two ECM-associated subtypes were identified by consensus clustering. Besides, an ECM-related prognostic model was validated to predict LUAD survival, and it was associated with the tumor immune microenvironment. Additional cross-analysis screened laminin subunit beta 1 (LAMB1) for further research. The survival time of LUAD patients with elevated LAMB1 expression was longer than those with low LAMB1 expression. Gene set enrichment analysis and CIBERSORT analyses revealed that LAMB1 expression correlated with tumor immune microenvironment. In conclusion, a prognostic model of LUAD patients depending on the ECM receptor interaction pathway was constructed. Screening out LAMB1 can become a prognostic risk factor for LUAD patients or a potential target during LUAD treatment.
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页数:11
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