Identification of two distinct head and neck squamous cell carcinoma subtypes based on fatty acid metabolism-related signatures: Implications for immunotherapy and chemotherapy
- Jianjun Zou 1, Yanbi Dai 2, Guangbo Xu 2, Yilong Kai 2, Lingfeng Lan 2, Junkun Zhang 2, Yufeng Wang 2
- Jianjun Zou 1, Yanbi Dai 2, Guangbo Xu 2
- 1Department of Otolaryngology, Hangzhou Red Cross Hospital (Zhejiang Hospital of Integrated Traditional Chinese and Western Medicine), Hangzhou, China.
- 2Department of Otolaryngology, The First People's Hospital of Yuhang District (The First Affiliated Hospital, Zhejiang University School of Medicine, Liangzhu Branch), Hangzhou, China.
- 0Department of Otolaryngology, Hangzhou Red Cross Hospital (Zhejiang Hospital of Integrated Traditional Chinese and Western Medicine), Hangzhou, China.
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View abstract on PubMed
Summary
This summary is machine-generated.This study identifies two molecular subtypes of head and neck squamous cell carcinoma (HNSCC) based on fatty acid metabolism genes. A novel 11-gene risk model and nomogram can predict patient prognosis and stratify risk, aiding treatment decisions.
Area Of Science
- Oncology
- Metabolomics
- Immunology
Background
- Lipid metabolism dysregulation is crucial in tumor initiation and progression.
- Head and neck squamous cell carcinoma (HNSCC) subtypes require molecular characterization for improved prognostication.
Purpose Of The Study
- To classify HNSCC molecular subtypes based on fatty acid metabolism.
- To develop a prognostic risk model and nomogram for HNSCC patients.
Main Methods
- Transcriptomic and clinical data from public databases were analyzed.
- Non-negative matrix factorization identified prognostic fatty acid metabolism genes (FAMGs).
- Cox regression and machine learning constructed a prognostic risk model and nomogram.
Main Results
- Two distinct HNSCC molecular subtypes were identified based on 3 FAMGs, showing prognostic and immune heterogeneity.
- An 11-gene risk model stratified patients into high- and low-risk groups with differential prognoses and immune infiltration.
- The risk model correlated with immune cell populations (B cells, T cells, macrophages, mast cells, dendritic cells).
Conclusions
- A novel molecular classification and prognostic risk model for HNSCC based on FAMGs were developed.
- FAMGs play a role in shaping the tumor immune microenvironment and influencing treatment response.
- The developed nomogram integrating risk signature and radiotherapy shows promise for HNSCC prognosis prediction.
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