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一项针对口腔咀嚼黏膜的表观基因组和转录组全基因组关联研究将 CYP1B1 确定为吸烟人群中上皮健康的核心因素。

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

机构信息

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.

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.

出版信息

Clin Epigenetics. 2019 Jul 22;11(1):105. doi: 10.1186/s13148-019-0697-y.

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) and two mapping to AHRR (aryl-hydrocarbon receptor repressor; best p = 5.9 × 10). 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. RNA-Seq data showed significantly increased expression of CYP1B1 in smokers compared to non-smokers (p = 2.2 × 10), 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.

摘要

背景

口腔黏膜在胃肠道和呼吸道的门户处维持屏障完整性方面起着重要作用。吸烟是导致常见口腔炎症性疾病牙周炎和口腔癌的一个强烈的环境风险因素。香烟烟雾会影响各种组织中的基因甲基化和表达。这是首次针对与吸烟相关的口腔咀嚼黏膜的生物活性甲基化标记物进行的全基因组关联研究(EWAS)。

结果

对 18 名当前吸烟者和 21 名从不吸烟者的口腔咀嚼黏膜活检组织进行了分析,使用 Infinium Methylation EPICBeadChip 芯片和相同样本的全转录组 RNA 测序(RNA-Seq;每个样本 1600 万条读数)进行了联合分析。我们在协方差分析(ANCOVA)中分析了 CpG 甲基化值与吸烟和吸烟包年(SPY)水平的相关性。有 9 个 CpG 与吸烟状态显著相关,其中 3 个 CpG 映射到 CYP1B1 的遗传区域(细胞色素 P450 家族 1 亚家族 B 成员 1;最佳 p=5.5×10),2 个映射到 AHRR(芳香烃受体抑制剂;最佳 p=5.9×10)。在 SPY 分析中,52 个基因座的 61 个 CpG 位点与吸烟量引起的甲基化值变化显著相关。其中,最显著的关联位于 CYP1B1 基因,p=4.0×10。与非吸烟者相比,吸烟者的 CYP1B1 表达明显增加(p=2.2×10),同时有 13 个转录本明显上调。6 个转录本下调。AHRR 无差异表达。体外研究表明,香烟烟雾提取物直接上调了牙龈成纤维细胞中 CYP1B1 的表达。

结论

本研究验证了 CYP1B1 和 AHRR 在烟草烟雾中异生物质代谢中的既定作用,并强调了这些基因的表观遗传调控的重要性。我们首次为口腔咀嚼黏膜提供了这一作用的证据。

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