DNA methylation biomarkers for head and neck squamous cell carcinoma. Issue 4 (3rd April 2018)

• Record Type: Journal Article
• Authors: Zhou, Chongchang; Ye, Meng; Ni, Shumin; Li, Qun; Ye, Dong; Li, Jinyun; Shen, Zhisen; Deng, Hongxia
• Is Part Of: Epigenetics. Volume 13:Issue 4(2018)
• Page Start: 398
• Page End: 409
• Publication Date: 2018-04-03
• Subjects: DNA methylation -- biomarker -- head and neck squamous cell carcinoma; Epigenesis -- Periodicals; Epigenetica; 572.86505
• DOI: 10.1080/15592294.2018.1465790
• Languages: English
• ISSNs: 1559-2294

Abstract

ABSTRACT: DNA methylation plays an important role in the etiology and pathogenesis of head and neck squamous cell carcinoma (HNSCC). The current study aimed to identify aberrantly methylated-differentially expressed genes (DEGs) by a comprehensive bioinformatics analysis. In addition, we screened for DEGs affected by DNA methylation modification and further investigated their prognostic values for HNSCC. We included microarray data of DNA methylation (GSE25093 and GSE33202) and gene expression (GSE23036 and GSE58911) from Gene Expression Omnibus. Aberrantly methylated-DEGs were analyzed with R software. The Cancer Genome Atlas (TCGA) RNA sequencing and DNA methylation (Illumina HumanMethylation450) databases were utilized for validation. In total, 27 aberrantly methylated genes accompanied by altered expression were identified. After confirmation by The Cancer Genome Atlas (TCGA) database, 2 hypermethylated-low-expression genes ( FAM135B and ZNF610 ) and 2 hypomethylated-high-expression genes ( HOXA9 and DCC ) were identified. A receiver operating characteristic (ROC) curve confirmed the diagnostic value of these four methylated genes for HNSCC. Multivariate Cox proportional hazards analysis showed that FAM135B methylation was a favorable independent prognostic biomarker for overall survival of HNSCC patients.