A Novel Signature of Necroptosis-Associated Genes as a Potential Prognostic Tool for Head and Neck Squamous Cell Carcinoma

被引:4
|
作者
Huang, Jing [1 ]
Huo, Hongqi [2 ]
Lu, Rong [3 ]
机构
[1] Fujian Med Univ, Fujian Canc Hosp, Dept Pharm, Canc Hosp, Fuzhou, Peoples R China
[2] Handan Cent Hosp, Nucl Med Dept, Handan, Peoples R China
[3] Xiamen Univ, Xiamen Key Lab Genet Testing, Sch Med, Dept Lab Med,Affiliated Hosp 1, Xiamen, Peoples R China
关键词
risk score; prognosis; squamous cell carcinoma; necroptosis; immune; tumor; DEATH DOMAIN; EXPRESSION; PROTEIN; CANCER; BNIP3; HYPOXIA; KINASE; AXL; METHYLATION; RECURRENT;
D O I
10.3389/fgene.2022.907985
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Head and neck squamous cell carcinoma (HNSCC) arises from squamous cells in the oral cavity, pharynx and larynx. Although HNSCC is sensitive to radiotherapy, patient prognosis is poor. Necroptosis is a novel programmed form of necrotic cell death. The prognostic value of necroptosis-associated gene expression in HNSCC has not been explored.Material and Methods: We downloaded mRNA expression data of HNSCC patients from TCGA databases and Gene Expression Omnibus (GEO) databases, and compared gene expression between tumor tissues and adjacent normal tissues to identify differentially expressed genes (DEGs) and necroptosis-related prognostic genes. A model with necroptosis-related genes was established to predict patient prognosis via LASSO method and Kaplan-Meier analysis. GSE65858 data set (n = 270) from GEO was used to verify the model's predictive ability. Gene set enrichment analyses, immune microenvironment analysis, principal component analysis, and anti-tumor compound IC50 prediction were also performed.Results: We identified 49 DEGs and found 10 DEGs were associated with patient survival (p < 0.05). A risk model of 6-gene signature was constructed using the TCGA training data set and further validated with the GEO data set. Patients in the low-risk group survived longer than those in the high-risk group (p < 0.05) in the GEO validation sets. Functional analysis showed the two patient groups were associated with distinct immunity conditions and IC50.Conclusion: We constructed a prognostic model with 6 necroptosis-associated genes for HNSCC. The model has potential usage to guide treatment because survival was different between the two groups.
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页数:11
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