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pmid:40497148

Identification and Validation of Oxidative Stress-Related Diagnostic Marker Genes and Immune Landscape in Ulcerative Interstitial Cystitis by Integrating Bioinformatics and Machine Learning.

Chaowei Fu · Yuwei Zhang · Yu Zhao · Shiyu Wang · Yuhua Zhou · Jing Lv · Shengkai Jin · Fengping Liu · Ninghan Feng

Journal of inflammation research · 2025 doi:10.2147/JIR.S524653

Paper

complete

Experiment

complete

Data

partial

Analysis

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Execution

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title
Identification and Validation of Oxidative Stress-Related Diagnostic Marker Genes and Immune Landscape in Ulcerative Interstitial Cystitis by Integrating Bioinformatics and Machine Learning.
doi
10.2147/JIR.S524653
pmid
40497148
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[0]
Chaowei Fu
[1]
Yuwei Zhang
[2]
Yu Zhao
[3]
Shiyu Wang
[4]
Yuhua Zhou
[5]
Jing Lv
[6]
Shengkai Jin
[7]
Fengping Liu
[8]
Ninghan Feng
journal
Journal of inflammation research
year
2025
abstract
Purpose: Interstitial cystitis (IC) is a chronic inflammatory disease with autoimmune associations, particularly in ulcerative IC, a severe and refractory subtype. Oxidative stress plays a crucial role in IC pathogenesis, interacting with inflammation and immune cell infiltration. This study aimed to identify oxidative stress-linked biomarkers and explore their relationship with immune cell infiltration to enhance diagnosis and treatment strategies. Patients and Methods: The GSE711783 dataset from GEO was analyzed to identify differentially expressed genes in ulcerative IC. Oxidative stress-related genes were sourced from GeneCards, with hub genes identified via WGCNA and protein-protein interaction networks. Diagnostic markers were refined using machine learning, and a nomogram prediction model was developed. Diagnostic biomarkers were validated in vitro and in vivo, immune infiltration was assessed with CIBERSORT, and potential therapeutic drugs were identified through DSigDB. Results: Four diagnostic biomarkers-BMP2, MMP9, CCK, and NOS3-were identified and found to be associated with immune cells, including CD4+ T cells and eosinophils. Decitabine was identified as a potential therapeutic candidate. Experimental validation confirmed the expression of these biomarkers. Conclusion: This study identifies BMP2, MMP9, CCK, and NOS3 as key biomarkers, offering valuable insights into the diagnosis and treatment of IC.
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The limma analysis of GSE11783 identified 1,893 differentially expressed genes between ulcerative IC and control samples.
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By applying statistical criteria (adj.P < 0.05 and |logFC| > 1), a total of 1893 DEGs were identified, comprising 823 up-regulated genes and 1070 down-regulated genes (Additional file 1: Table S2).
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To identify the differentially expressed genes (DEGs) in the GSE11783 dataset, we first normalized the raw expression matrix using R software (version 4.3.3). Subsequently, we employed the “limma (version 3.56.2)” package to conduct a comprehensive analysis of gene expression between IC and controls.
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sections[22] "Identification of the DEGs of IC" paragraph 2
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Gene expression profile of bladder tissue of patients with ulcerative interstitial cystitis
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ostic biomarkers were validated in vitro and in vivo, immune infiltration was assessed with CIBER
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Complete file
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