Heterogeneity analysis and prognostic model construction of HPV negative oral squamous cell carcinoma T cells using ScRNA-seq and bulk-RNA analysis
- Chunyan Li 1, Zengbo Lv 1, Chongxin Li 1, Shixuan Yang 1, Feineng Liu 1, Tengfei Zhang 1, Lin Wang 1, Wen Zhang 1, Ruoyu Deng 1, Guoyu Xu 1, Huan Luo 1, Yinhong Zhao 1, Jialing Lv 2, Chao Zhang 3
- Chunyan Li 1, Zengbo Lv 1, Chongxin Li 1
- 1Department of Oncology, the First People's Hospital of Qujing City/the Qujing Affiliated Hospital of Kunming Medical University, 1 Yuanlin Road, Qujing, Yunnan, China.
- 2Department of Oncology, the First People's Hospital of Qujing City/the Qujing Affiliated Hospital of Kunming Medical University, 1 Yuanlin Road, Qujing, Yunnan, China. lvjialinglvjialing@126.com.
- 3Department of Oncology, the First People's Hospital of Qujing City/the Qujing Affiliated Hospital of Kunming Medical University, 1 Yuanlin Road, Qujing, Yunnan, China. chesanjin@163.com.
- 0Department of Oncology, the First People's Hospital of Qujing City/the Qujing Affiliated Hospital of Kunming Medical University, 1 Yuanlin Road, Qujing, Yunnan, China.
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View abstract on PubMed
Summary
This summary is machine-generated.This study identifies T-cell marker genes to predict survival and immune infiltration in human papilloma virus (HPV)-negative oral squamous cell carcinoma (OSCC). A novel risk model aids in understanding T-cell roles in HPV-negative OSCC prognosis.
Area Of Science
- Oncology
- Immunology
- Genomics
Background
- T cells play a crucial role in tumor development and the tumor microenvironment (TME).
- Human papilloma virus (HPV)-negative oral squamous cell carcinoma (OSCC) is a significant health concern.
- Understanding T-cell dynamics is vital for predicting OSCC progression and treatment response.
Purpose Of The Study
- To analyze T-cell marker gene expression profiles in HPV-negative OSCC.
- To develop a predictive risk model for HPV-negative OSCC using T-cell genes.
- To investigate the link between the risk score and immunotherapy response.
Main Methods
- Single-cell RNA sequencing (scRNA-seq) of HPV-negative OSCC samples.
- Cell-cell communication, trajectory, and pathway enrichment analyses.
- Construction and validation of a T-cell-associated gene prognostic model using TCGA and GEO data.
- Assessment of immune infiltration and qRT-PCR validation of key genes.
Main Results
- Identified 774 differentially expressed T-cell-associated genes across five subtypes.
- Developed a prognostic model predicting survival and TME immune infiltration.
- High-risk group showed significantly upregulated expression of PMEPA1, SH2D2A, SMS, and PRDX4 compared to the low-risk group.
Conclusions
- The study offers a valuable resource for understanding T-cell heterogeneity in HPV-negative OSCC.
- Prognostic risk models based on T-cell genes provide insights into survival and immune infiltration.
- Findings may guide personalized treatment strategies for HPV-negative OSCC patients.
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