Analysis of methylation‐driven genes for predicting the prognosis of patients with head and neck squamous cell carcinoma
Autor: | Lanxin Cheng, Yidan Song, Hongdan Xu, Yihua Pan, Jun Liu |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Oncology medicine.medical_specialty medicine.medical_treatment Biochemistry Targeted therapy 03 medical and health sciences 0302 clinical medicine Internal medicine Biomarkers Tumor medicine Humans Gene Regulatory Networks Epigenetics Molecular Biology Survival rate Gene Survival analysis Receiver operating characteristic Sequence Analysis RNA Squamous Cell Carcinoma of Head and Neck business.industry Gene Expression Profiling Cell Biology Methylation DNA Methylation Prognosis medicine.disease Head and neck squamous-cell carcinoma Gene Expression Regulation Neoplastic Survival Rate 030104 developmental biology Head and Neck Neoplasms 030220 oncology & carcinogenesis business |
Zdroj: | Journal of Cellular Biochemistry. 120:19482-19495 |
ISSN: | 1097-4644 0730-2312 |
DOI: | 10.1002/jcb.29252 |
Popis: | To help provide evidence for prognosis prediction and personalized targeted therapy for patients with head and neck squamous cell carcinoma (HNSCC), we investigated prognosis-specific methylation-driven genes in HNSCC. Survival time data, RNA sequencing data, and methylation data for HNSCC patients were downloaded from The Cancer Genome Atlas. The MethylMix R package based on the β mixture model was utilized to screen genes with different methylation statuses in tumor tissues and adjacent normal tissues, and a total of 182 HNSCC-related methylation-driven genes were then identified. A survival prediction scoring model based on multivariate Cox analysis was developed to screen the genes related to the prognosis of HNSCC, and a linear risk model of the methylation status of six genes (INA, LINC01354, TSPYL4, MAGEB2, EPHX3, and ZNF134) was constructed. The prognostic values of the six genes were further independently explored by survival analysis combined with methylation and gene expression analyses. The 5-year survival rate in the high-risk group of patients in the test set was 30.4% (95% CI: 22.7%-40.8%) and that in the low-risk group of patients was 65.5% (95% CI: 56.1%-76.5%). The area under the receiver operating characteristic curve for the model was 0.723, which further verified the specificity and sensitivity of the model. In addition, subsequent combined survival analysis revealed that all six genes could be used as independent prognostic markers and thus might be potential drug targets. The innovative method provides new insight into the molecular mechanism and prognosis of HNSCC. |
Databáze: | OpenAIRE |
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