4.4 Article

An Oxidative Stress-Related Genes Signature for Predicting Survival in Bladder Cancer: Based on TCGA Database and Bioinformatics

Journal

INTERNATIONAL JOURNAL OF GENERAL MEDICINE
Volume 15, Issue -, Pages 2645-2667

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/IJGM.S348945

Keywords

bladder cancer; oxidative stress; prognosis; risk signature; immune cell infiltration; drug sensitivity

Funding

  1. National Science Foundation of China [81960342]
  2. Natural Science Foundation of Guangxi
  3. Health Department Fund Project of Guangxi Province [z20201184]

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This study developed an OS-related genes signature for predicting overall survival and impacting the immune status in bladder cancer (BC) patients. The new nomogram integrating the risk score with TNM stage showed superior predictive value in forecasting the survival rate of BC patients. The study highlighted the significant role of immune cells and functions in carcinogenesis and development, and the levels of expression of prognostic genes were shown to be substantially linked with drug sensitivity.
Background: Oxidative stress (OS) responses have been linked to oncogenesis and tumor progression and have recently been regarded as a potential strategy for tumor therapy. However, OS-related therapeutic targets have not been identified to date in the bladder cancer (BC). Methods: The mRNA expression and clinical data of BC were downloaded from the public database. Prognostic risk score signature was constructed using LASSO Cox regression analysis. External validation was performed in GSE15307 cohort. ESTIMATE, CIBERSORT, and ssGSEA algorithm were used to analyze immune cell infiltration and immune microenvironment. Next, functional enrichment analysis was performed to elucidate the mechanism underlying the signature. Additionally, we performed a nomogram to forecast the survival rate of individual BC patients. Results: An OS-related genes (OSRGs) signature was constructed. Overall survival was lower in the high-risk group than in the low-risk group, according to survival analyses. The area under the curve (AUC) of ROC curves further validated the prognostic signature's strong prediction performance in these two cohorts. The risk score was verified as an independent risk factor for BC by independent prognostic analysis. Moreover, as compared to TNM stage alone, a nomogram that integrated the risk score with TNM stage showed a much superior predictive value. Immune infiltration and tumor microenvironment studies indicated that immune cells and functions may play a significant role in carcinogenesis and development. The levels of expression of prognostic genes were shown to be substantially linked with drug sensitivity. Conclusion: We developed a novel OSRGs signature for predicting overall survival and impacting the immune status in patients with BC. New nomogram can help clinicians predict the survival rate of BC patients. These findings shed new light on the potential usage of OSRGs signature in BC patients.

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