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Updated: Jan 6, 2026
Isolation and Characterization of a Head and Neck Squamous Cell Carcinoma Subpopulation Having Stem Cell Characteristics
Published on: May 11, 2016
Sphingolipid metabolism patterns reveal distinct prognostic and immune landscapes in head and neck squamous cell
Bingtong Yue1, Huiqian Zhang2, Zhuoran Li3
1Department of Pathophysiology, School of Basic Medical Sciences, Medical College, Zhengzhou University, Zhengzhou, Henan Province 450001, PR China; The First Clinical Medical College of Zhengzhou University, Zhengzhou, Henan Province 450001, PR China.
Background:
Head and neck squamous cell carcinoma (HNSCC) remains a global public health concern due to its poor prognosis and high mortality. Sphingolipids, integral components of cell membranes, are emerging as potential therapeutic targets in cancer because of their critical roles in oncogenic signaling. However, a prognostic model based on sphingolipid metabolism in HNSCC with immune implications is still lacking.
Methods:
We obtained transcriptomic and clinical data for HNSCC from TCGA and GEO databases, and retrieved sphingolipid metabolism-related genes from MSigDB. Qualitatively, HNSCC patients were categorized via unsupervised consensus clustering. Quantitatively, a risk model was constructed using Lasso regression. In addition, single-cell RNA sequencing analysis was performed for further investigation. Finally, the core gene of the risk model was identified by WGCNA analysis, and then validated by qRT-PCR and IHC in clinical specimens.
Results:
We developed a novel five-gene prognostic signature (SPNS2, NEU1, B4GALNT1, CSNK1G2, and ARSI) to predict outcomes in HNSCC. Furthermore, the high-risk group exhibited a decreased immune infiltration level and a suppressive microenvironment. Immunotherapy response analysis further demonstrated the clinical utility of this risk stratification in guiding treatment decisions. Moreover, the core gene B4GALNT1 was confirmed to be highly expressed in clinical HNSCC samples.
Conclusions:
This study is the first to establish a sphingolipid metabolism-based five-gene signature in HNSCC. Its superior reliability and accuracy in predicting prognosis and immune response offer new clinical perspectives.
