Heterogeneity analysis and prognostic model construction of HPV negative oral squamous cell carcinoma T cells using ScRNA-seq and bulk-RNA analysis

  • 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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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.