dc.contributor.author
Richter, Gesa M.
dc.contributor.author
Kruppa, Jochen
dc.contributor.author
Munz, Matthias
dc.contributor.author
Wiehe, Ricarda
dc.contributor.author
Häsler, Robert
dc.contributor.author
Franke, Andre
dc.contributor.author
Martins, Orlando
dc.contributor.author
Jockel-Schneider, Yvonne
dc.contributor.author
Bruckmann, Corinna
dc.contributor.author
Dommisch, Henrik
dc.contributor.author
Schaefer, Arne S.
dc.date.accessioned
2019-08-05T11:38:59Z
dc.date.available
2019-08-05T11:38:59Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/25226
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-3930
dc.description.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.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
epigenome-wide association study (EWAS)
en
dc.subject
masticatory mucosa
en
dc.subject
cytochrome P 450 pathway
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
A combined epigenome- and transcriptome-wide association study of the oral masticatory mucosa assigns CYP1B1 a central role for epithelial health in smokers
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
105
dcterms.bibliographicCitation.doi
10.1186/s13148-019-0697-y
dcterms.bibliographicCitation.journaltitle
Clinical Epigenetics
dcterms.bibliographicCitation.originalpublishername
BMC
dcterms.bibliographicCitation.volume
11
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
31331382
dcterms.isPartOf.eissn
1868-7083