Predicting biomarkers in laryngeal squamous cell carcinoma based on the cytokine-cytokine receptor interaction pathway
- Qingyong Chen 1, Dongqing Wang 2, Zhipeng Chen 2, Liqiang Lin 2, Qiang Shao 2, Han Zhang 3, Peng Li 2, Huaiqing Lv 2
- Qingyong Chen 1, Dongqing Wang 2, Zhipeng Chen 2
- 1The Second School of Clinical Medicine of Binzhou Medical University, Yan Tai, China.
- 2Department of Otorhinolaryngology, Linyi People's Hospital, Linyi, China.
- 3No.One Clinical Medicine School of Binzhou Medical University, Bing Zhou, China.
- 0The Second School of Clinical Medicine of Binzhou Medical University, Yan Tai, China.
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View abstract on PubMed
Summary
This summary is machine-generated.Bioinformatics identified seven differentially expressed genes in the cytokine-cytokine receptor interaction (CCRI) pathway. Mendelian randomization confirmed cytokine receptors as a risk factor for laryngeal squamous cell carcinoma (LSCC), offering new therapeutic targets.
Area Of Science
- Oncology
- Genetics
- Bioinformatics
Background
- Laryngeal squamous cell carcinoma (LSCC) is a significant health concern.
- Identifying molecular pathways and biomarkers is crucial for understanding LSCC pathogenesis.
- The cytokine-cytokine receptor interaction (CCRI) pathway's role in LSCC requires further investigation.
Purpose Of The Study
- To identify differentially expressed genes within the CCRI pathway in LSCC.
- To validate potential biomarkers for LSCC using bioinformatics and Mendelian randomization (MR).
- To explore the causal relationship between cytokine receptors and LSCC risk.
Main Methods
- Downloaded and analyzed LSCC-related gene expression datasets from the GEO database.
- Screened for differentially expressed genes in the CCRI pathway.
- Performed two-way Mendelian randomization to assess the causal link between cytokine receptors and LSCC.
- Utilized multiple databases (DGIdb, Miranda, etc.) to analyze gene-drug, gene-immune cell, and gene-RNA interactions.
Main Results
- Identified seven differentially expressed genes (CD27, CXCL2, CXCL9, INHBA, IL6, CXCL11, TNFRSF17) in the CCRI pathway.
- MR analysis indicated that CCRI receptors are a risk factor for LSCC (OR = 1.629, P = 0.026).
- The identified genes showed correlations with drug responses, immune cell infiltration, and RNA interactions.
- Validation set analysis confirmed the differential gene expression findings.
Conclusions
- Differential gene expression in the CCRI pathway was identified in LSCC.
- Mendelian randomization supports cytokine receptors as risk factors for LSCC.
- These findings offer novel insights into LSCC pathogenesis and potential therapeutic targets.
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