Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/106862
Title: A combined epigenome- and transcriptome-wide association study of the oral masticatory mucosa assigns CYP1B1 a central role for epithelial health in smokers
Authors: Richter, Gesa M.
Kruppa, Jochen
Munz, Matthias
Wiehe, Ricarda
Häsler, Robert
Franke, Andre
Martins, Orlando 
Jockel-Schneider, Yvonne
Bruckmann, Corinna
Dommisch, Henrik
Schaefer, Arne S.
Keywords: EWAS; Methylation; Expression; Masticatory mucosa; CYP1B1; AHRR; Cytochrome P 450 pathway; OSCC; Smoking
Issue Date: 22-Jul-2019
Publisher: Springer Nature
Serial title, monograph or event: Clinical Epigenetics
Volume: 11
Issue: 1
Abstract: Background: The oral mucosa has an important role in maintaining barrier integrity at the gateway to the gastrointestinal and respiratory tracts. Smoking is a strong environmental risk factor for the common oral inflammatory disease periodontitis and oral cancer. Cigarette smoke affects gene methylation and expression in various tissues. This is the first epigenome-wide association study (EWAS) that aimed to identify biologically active methylation marks of the oral masticatory mucosa that are associated with smoking. Results: Ex vivo biopsies of 18 current smokers and 21 never smokers were analysed with the Infinium Methylation EPICBeadChip and combined with whole transcriptome RNA sequencing (RNA-Seq; 16 mio reads per sample) of the same samples. We analysed the associations of CpG methylation values with cigarette smoking and smoke pack year (SPY) levels in an analysis of covariance (ANCOVA). Nine CpGs were significantly associated with smoking status, with three CpGs mapping to the genetic region of CYP1B1 (cytochrome P450 family 1 subfamily B member 1; best p = 5.5 × 10−8) and two mapping to AHRR (aryl-hydrocarbon receptor repressor; best p = 5.9 × 10−9). In the SPY analysis, 61 CpG sites at 52 loci showed significant associations of the quantity of smoking with changes in methylation values. Here, the most significant association located to the gene CYP1B1, with p = 4.0 × 10−10. RNA-Seq data showed significantly increased expression of CYP1B1 in smokers compared to non-smokers (p = 2.2 × 10−14), together with 13 significantly upregulated transcripts. Six transcripts were significantly downregulated. No differential expression was observed for AHRR. In vitro studies with gingival fibroblasts showed that cigarette smoke extract directly upregulated the expression of CYP1B1. Conclusion: This study validated the established role of CYP1B1 and AHRR in xenobiotic metabolism of tobacco smoke and highlights the importance of epigenetic regulation for these genes. For the first time, we give evidence of this role for the oral masticatory mucosa.
URI: https://hdl.handle.net/10316/106862
ISSN: 1868-7075
1868-7083
DOI: 10.1186/s13148-019-0697-y
Rights: openAccess
Appears in Collections:FMUC Med. Dentária - Artigos em Revistas Internacionais

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