Immunotherapy has been demonstrated favorable in head and neck squamous cell carcinoma (HNSCC). Studies indicated that immune-related gene prognostic index (IRGPI) was a robust signature, and N-methyladenosine (mA) methylation had a significant impact on the tumor immune microenvironment (TIME) and immunotherapy of head and neck squamous cell carcinoma. Thus, combining indicated that immune-related gene prognostic index with mA status should offer a better predictive power for immune responses. Head and neck squamous cell carcinoma samples from the cancer genome atlas (TCGA, = 498) and gene expression omnibus database (GSE65858, = 270) were used in this study. Cox regression analysis was used to construct the indicated that immune-related gene prognostic index through immune-related hub genes which were identified by weighted gene co-expression network analysis (WGCNA). The mA risk score was constructed by least absolute shrinkage and selection operator (LASSO) regression analysis. Principal component analysis was used to construct a composite score, and systematically correlate subgroups according to tumor immune microenvironment cell-infiltrating characteristics. A composite score was determined based on indicated that immune-related gene prognostic index and mA risk score. Head and neck squamous cell carcinoma patients in the cancer genome atlas were divided into four subgroups: A (IRGPI-High&mA-risk-High, = 127), B (IRGPI-High&mA-risk-Low, = 99), C (IRGPI-Low&mA-risk-High, = 99), and D (IRGPI-Low&mA-risk-Low, = 128), and overall survival (OS) was significantly different between subgroups ( < 0.001). The characteristics of tumor immune microenvironment cell infiltration in the four subgroups were significantly different in subgroups ( < 0.05). The receiver operating characteristic (ROC) curves show the predictive value of composite score for overall survival was superior to other scores. The composite score is a promising prognostic signature which might distinguish immune and molecular characteristics, predict prognosis, and guide more effective immunotherapeutic strategies for head and neck squamous cell carcinoma.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9948032 | PMC |
http://dx.doi.org/10.3389/fgene.2023.1061569 | DOI Listing |
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