Integrated virus-host methylome analysis in head and neck squamous cell carcinoma

• Published in: Epigenetics 2013-09, Vol.8 (9), p.953-961
• Main Authors: Wilson, Gareth A, Lechner, Matthias, Köferle, Anna, Caren, Helena, Butcher, Lee M, Feber, Andrew, Fenton, Tim, Jay, Amrita, Boshoff, Chris, Beck, Stephan
• Format: Article
• Language: English
• Subjects: Cadherins - genetics; Carcinoma, Squamous Cell - genetics; Carcinoma, Squamous Cell - metabolism; Carcinoma, Squamous Cell - virology; Cell Line, Tumor; DNA Methylation; DNA-Binding Proteins - physiology; Epigenesis, Genetic; epigenome; Genome, Human; Genome, Viral; Head and Neck Neoplasms - genetics; Head and Neck Neoplasms - metabolism; Head and Neck Neoplasms - virology; head and neck squamous cell carcinoma (HNSCC); human papillomavirus (HPV); Human papillomavirus 16 - genetics; Human papillomavirus 16 - physiology; Humans; methylome; Oligonucleotide Array Sequence Analysis; Oncogene Proteins, Viral - physiology; Research Paper; Squamous Cell Carcinoma of Head and Neck; Tumor Cells, Cultured; Virus Integration - genetics
• ISSN: 1559-2294; 1559-2308; 1559-2308
• DOI: 10.4161/epi.25614

One in six cancers worldwide is caused by infection and human papillomavirus (HPV) is one of the main culprits. To better understand the dynamics of HPV integration and its effect on both the viral and host methylomes, we conducted whole-genome DNA methylation analysis using MeDIP-seq of HPV+ and HPV- head and neck squamous cell carcinoma (HNSCC). We determined the viral subtype to be HPV-16 in all cases and show that HPV-16 integrates into the host genome at multiple random sites and that this process predominantly involves the transcriptional repressor gene (E2) in the viral genome. Comparative analysis identified 453 (FDR ≤ 0.01) differentially methylated regions (DMRs) in the HPV+ host methylome. Bioinformatics characterization of these DMRs confirmed the previously reported cadherin genes to be affected but also revealed new targets for HPV-mediated methylation changes at regions not covered by array-based platforms, including the recently identified super-enhancers.