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• W4312069352 abstract "Abstract Background: Cellular senescence refers to cells entering a relatively stable state of cell cycle arrest, which is a barrier that tumor cells must cross to achieve immortalization and plays an extremely important role in preventing the occurrence and development of tumors. In recent years, numerous studies have shown that inducing tumor cells to enter a senescent state has become a feasible tumor control strategy. At present, cellular senescence has become a research hotspot in tumor prevention and treatment, as well as in cell biology. However, the expression and prognostic values of cellular senescence genes in head and neck squamous cell carcinoma (HNSC) remain unclear. Material/Methods: We analyzed the expression patterns and prognostic values of cellular senescence genes in HNSC from TCGA and GEO. The TCGA-HNSC data wereused as the training group and were divided into high- and low-risk groups, and the GEO database was used as the test group. Analyses included survival analysis, ROC curve analysis, risk curve analysis, independent prognostic analysis and model validation for clinical grouping. We used the HPA database for protein-level validation of the genes. Results: We identified 5 cellular senescence genes associated with HNSC, namely,BTG3, EHF, EZH2, TACC3 and TXN. These cellular senescence genes were analyzed in the training and test groups and were found to be significantly associated with the prognosis of HNSC patients. Conclusions: The tumor immune microenvironment of HNSC is closely related to cellular senescence-related features. Cellular senescence genes (BTG3, EHF, EZH2, TACC3, and TXN) have the potential to be diagnostic and prognostic biomarkers for HNSC." @default.
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• W4312069352 date "2022-12-21" @default.
• W4312069352 modified "2023-10-16" @default.
• W4312069352 title "Expression and prognosis of cellular senescence genes in head and neck squamous cell carcinoma" @default.
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• W4312069352 doi "https://doi.org/10.21203/rs.3.rs-2348895/v1" @default.
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