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pmid:37689745
Identification of molecular subgroups and establishment of risk model based on the response to oxidative stress to predict overall survival of patients with lung adenocarcinoma.
Linzhuang Liu · Qinghua Hou · Baorong Chen · Xiyi Lai · Hanwen Wang · Haozhen Liu · Liusheng Wu · Sheng Liu · Kelin Luo · Jixian Liu
European journal of medical research · 2023 doi:10.1186/s40001-023-01290-5
Paper
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Experiment
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Data
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Analysis
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Complete file
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However, the specific association between lung cancer and oxidative stress is unclear. This study aimed to investigate the role of oxidative stress in the progression and prognosis of lung adenocarcinoma (LUAD).\nMETHODS: The gene expression profiles and corresponding clinical information were collected from GEO and TCGA databases. Differentially expressed oxidative stress-related genes (OSRGs) were identified between normal and tumor samples. Consensus clustering was applied to identify oxidative stress-related molecular subgroups. Functional enrichment analysis, GSEA, and GSVA were performed to investigate the potential mechanisms. xCell was used to assess the immune status of the subgroups. A risk model was developed by the LASSO algorithm and validated using TCGA-LUAD, GSE13213, and GSE30219 datasets.\nRESULTS: A total of 40 differentially expressed OSRGs and two oxidative stress-associated subgroups were identified. Enrichment analysis revealed that cell cycle-, inflammation- and oxidative stress-related pathways varied significantly in the two subgroups. Furthermore, a risk model was developed and validated based on the OSRGs, and findings indicated that the risk model exhibits good prediction and diagnosis values for LUAD patients.\nCONCLUSION: The risk model based on the oxidative stress could act as an effective prognostic tool for LUAD patients. 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