Single-cell RNA sequencing and traditional RNA sequencing reveals the role of cancer-associated fibroblasts in head and neck squamous cell carcinomas cohort.

backgroundHead and neck squamous cell carcinomas (HNSCs) are among the most common tumors worldwide. Despite the availability of various diagnostic and therapeutic strategies, the incidence and mortality rates of HNSC remain high. Cancer-associated fibroblasts (CAFs), as a major component of the tumor microenvironment, exhibit diverse biological characteristics in terms of origin, genetics, and phenotype, and have been increasingly recognized for their roles in tumor progression.

methodsTo investigate the potential role of CAFs in HNSC, we performed a comprehensive bioinformatics analysis based on the TCGA HNSC cohort. We applied single-sample gene set enrichment analysis (ssGSEA), single-cell RNA sequencing (scRNA-seq) analysis, differential expression analysis, Cox regression, LASSO regression, and pathway enrichment analysis to identify CAF-related genes and assess their prognostic value.

resultsWe successfully identified a set of CAF-related genes and stratified the HNSC patients into high- and low-CAF groups. Based on the expression of these genes, we constructed a prognostic prediction model using LASSO and multivariate Cox regression analyses. A nomogram integrating the risk score and clinical characteristics was developed to improve individualized survival prediction. Enrichment analysis revealed that the type I interferon signaling pathway, cellular response to type I interferon, defense response to symbiont, and extracellular matrix organization were significantly associated with CAFs in HNSC.

conclusionOur study provides a novel CAF-based prognostic model and nomogram for predicting patient outcomes in HNSC. These findings highlight the importance of CAFs in the tumor microenvironment and their potential as therapeutic and prognostic biomarkers.