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      A combined epigenome- and transcriptome-wide association study of the oral masticatory mucosa assigns CYP1B1 a central role for epithelial health in smokers

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          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.

          Electronic supplementary material

          The online version of this article (10.1186/s13148-019-0697-y) contains supplementary material, which is available to authorized users.

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          Most cited references33

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            Phenotypic plasticity and the epigenetics of human disease.

            It is becoming clear that epigenetic changes are involved in human disease as well as during normal development. A unifying theme of disease epigenetics is defects in phenotypic plasticity--cells' ability to change their behaviour in response to internal or external environmental cues. This model proposes that hereditary disorders of the epigenetic apparatus lead to developmental defects, that cancer epigenetics involves disruption of the stem-cell programme, and that common diseases with late-onset phenotypes involve interactions between the epigenome, the genome and the environment. Increased understanding of epigenetic-disease mechanisms could lead to disease-risk stratification for targeted intervention and to targeted therapies.
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              50-year trends in smoking-related mortality in the United States.

              The disease risks from cigarette smoking increased in the United States over most of the 20th century, first among male smokers and later among female smokers. Whether these risks have continued to increase during the past 20 years is unclear. We measured temporal trends in mortality across three time periods (1959-1965, 1982-1988, and 2000-2010), comparing absolute and relative risks according to sex and self-reported smoking status in two historical cohort studies and in five pooled contemporary cohort studies, among participants who became 55 years of age or older during follow-up. For women who were current smokers, as compared with women who had never smoked, the relative risks of death from lung cancer were 2.73, 12.65, and 25.66 in the 1960s, 1980s, and contemporary cohorts, respectively; corresponding relative risks for male current smokers, as compared with men who had never smoked, were 12.22, 23.81, and 24.97. In the contemporary cohorts, male and female current smokers also had similar relative risks for death from chronic obstructive pulmonary disease (COPD) (25.61 for men and 22.35 for women), ischemic heart disease (2.50 for men and 2.86 for women), any type of stroke (1.92 for men and 2.10 for women), and all causes combined (2.80 for men and 2.76 for women). Mortality from COPD among male smokers continued to increase in the contemporary cohorts in nearly all the age groups represented in the study and within each stratum of duration and intensity of smoking. Among men 55 to 74 years of age and women 60 to 74 years of age, all-cause mortality was at least three times as high among current smokers as among those who had never smoked. Smoking cessation at any age dramatically reduced death rates. The risk of death from cigarette smoking continues to increase among women and the increased risks are now nearly identical for men and women, as compared with persons who have never smoked. Among men, the risks associated with smoking have plateaued at the high levels seen in the 1980s, except for a continuing, unexplained increase in mortality from COPD.
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                Author and article information

                Contributors
                +49 30 450 562 343 , gesa.richter@charite.de
                jochen.kruppa@charite.de
                m.munz@uni-luebeck.de
                ricarda.wiehe@charite.de
                r.haesler@mucosa.de
                a.franke@mucosa.de
                opmartins@fmed.uc.pt
                jockel_y@ukw.de
                corinna.bruckmann@meduniwien.ac.at
                henrik.dommisch@charite.de
                arne.schaefer@charite.de
                Journal
                Clin Epigenetics
                Clin Epigenetics
                Clinical Epigenetics
                BioMed Central (London )
                1868-7075
                1868-7083
                22 July 2019
                22 July 2019
                2019
                : 11
                : 105
                Affiliations
                [1 ]Department of Periodontology and Synoptic Dentistry, Institute for Dental and Craniofacial Sciences, Charité – Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Aßmannshauser Str. 4-6, 14197 Berlin, Germany
                [2 ]ISNI 0000 0001 2248 7639, GRID grid.7468.d, Institute for Biometry and Clinical Epidemiology, Charité – Universitätsmedizin Berlin, Freie Universität Berlin, , Humboldt-Universität zu Berlin, and Berlin Institute of Health, ; Charitéplatz 1, 10117 Berlin, Germany
                [3 ]ISNI 0000 0001 0057 2672, GRID grid.4562.5, Medical Systems Biology Group, Institute of Experimental Dermatology, Institute for Cardiogenetics, , University of Lübeck, ; 23562 Lübeck, Germany
                [4 ]ISNI 0000 0001 2153 9986, GRID grid.9764.c, Institute of Clinical Molecular Biology, , Christian-Albrechts-University, ; Rosalind-Franklin-Straße 12, 24105 Kiel, Germany
                [5 ]ISNI 0000 0000 9511 4342, GRID grid.8051.c, Institute of Periodontology, Dentistry Department, Faculty of Medicine, , University of Coimbra, ; Av. Bissaya Barreto, Bloco de Celas, 3000-075 Coimbra, Portugal
                [6 ]ISNI 0000 0001 1958 8658, GRID grid.8379.5, Department of Periodontology, Clinic of Preventive Dentistry and Periodontology, , University Medical Center of the Julius-Maximilians-University, ; Pleicherwall, 97070 Würzburg, Germany
                [7 ]ISNI 0000 0000 9259 8492, GRID grid.22937.3d, Department of Conservative Dentistry and Periodontology, , Medical University Vienna, School of Dentistry, ; Sensengasse 2a, 1090 Vienna, Austria
                Author information
                http://orcid.org/0000-0002-4825-4670
                Article
                697
                10.1186/s13148-019-0697-y
                6647091
                31331382
                b2bccf7c-1831-41fe-bfeb-b812086ae593
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 23 January 2019
                : 18 June 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001659, Deutsche Forschungsgemeinschaft;
                Award ID: RI 2827/1-1
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100002347, Bundesministerium für Bildung und Forschung;
                Award ID: 01DL15002
                Funded by: Deutsche Gesellschaft für Parodontologie/CP GABA
                Award ID: 2015
                Categories
                Research
                Custom metadata
                © The Author(s) 2019

                Genetics
                ewas,methylation,expression,masticatory mucosa,cyp1b1,ahrr,cytochrome p 450 pathway,oscc,smoking
                Genetics
                ewas, methylation, expression, masticatory mucosa, cyp1b1, ahrr, cytochrome p 450 pathway, oscc, smoking

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