» Articles » PMID: 33097495

An Immune-Related Gene Prognostic Index for Head and Neck Squamous Cell Carcinoma

Overview
Journal Clin Cancer Res
Specialty Oncology
Date 2020 Oct 24
PMID 33097495
Citations 143
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: To construct an immune-related gene prognostic index (IRGPI) for head and neck squamous cell carcinoma (HNSCC) and clarify the molecular and immune characteristics and the benefit of immune checkpoint inhibitor (ICI) therapy in IRGPI-defined subgroups of HNSCC.

Experimental Design: On the basis of The Cancer Genome Atlas HNSCC immune dataset ( = 546), 22 immune-related hub genes were identified by weighted gene coexpression network analysis. Three genes were identified to construct an IRGPI by using the Cox regression method and validated with the Gene Expression Omnibus (GEO) dataset ( = 270). Afterward, the molecular and immune characteristics and the benefit of ICI therapy in IRGPI-defined subgroups were analyzed.

Results: The IRGPI was constructed on the basis of , , and genes. IRGPI-high patients had a better overall survival than IRGPI-low patients, consistent with the results in the GEO cohort. The comprehensive results showed that a high IRGPI score was correlated with DNA repair-related pathways; low mutation rate; high infiltration of CD8 T cells, CD4 T cells, and M1 macrophages; active immunity and less aggressive phenotypes; and more benefit from ICI therapy. In contrast, a low IRGPI score was associated with cancer and metastasis-related pathways; high and mutation rate; high infiltration of B cells, M0 macrophages, and M2 macrophages; suppressive immunity and more aggressive phenotypes; and less benefit from ICI therapy.

Conclusions: IRGPI is a promising biomarker to distinguish the prognosis, the molecular and immune characteristics, and the immune benefit from ICI therapy in HNSCC.

Citing Articles

Melanoma Cell Adhesion Molecule Plays a Pivotal Role in Proliferation, Migration, Tumor Immune Microenvironment, and Immunotherapy in Colorectal Cancer.

Zhou J, Liu J, Yu Y, Nie H, Hong Y, Ning Y Cancer Med. 2025; 14(5):e70740.

PMID: 40042109 PMC: 11880918. DOI: 10.1002/cam4.70740.


Multiple mechanisms and applications of tertiary lymphoid structures and immune checkpoint blockade.

Li Z, Liu S, Liu D, Yang K, Xiong J, Fang Z J Exp Clin Cancer Res. 2025; 44(1):84.

PMID: 40038799 PMC: 11881293. DOI: 10.1186/s13046-025-03318-6.


Exploring the role of TIGIT in patients with Small Cell Lung Cancer as a novel predictor of prognosis and immunotherapy response.

Liu L, Wu P, Wang B, Dong J, Zhang C, Liu W Cancer Immunol Immunother. 2025; 74(4):134.

PMID: 40035834 PMC: 11880484. DOI: 10.1007/s00262-025-03985-6.


Bulk and Single-Cell Transcriptomic Reveals Shared Key Genes and Patterns of Immune Dysregulation in Both Intestinal Inflammatory Disease and Sepsis.

Liu C, Liu J, Yang Y J Cell Mol Med. 2025; 29(4):e70415.

PMID: 39993996 PMC: 11850196. DOI: 10.1111/jcmm.70415.


LRRC25 Is a Potential Biomarker for Predicting Immunotherapy Response in Patients with Gastric Cancer.

Yang Z, Yu B, Hu J, Jiang L, Jian M Dig Dis Sci. 2025; .

PMID: 39961962 DOI: 10.1007/s10620-025-08882-7.