Epigenomic Dysregulation in Youth Vapers: Implications for Disease Risk Assessment.

IF 5.9 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Stella Tommasi, Luciano Brocchieri, Silvia Tornaletti, Ahmad Besaratinia
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引用次数: 0

Abstract

Despite the ongoing epidemic of youth vaping, the long-term health consequences of electronic cigarette use are largely unknown. We report the effects of vaping versus smoking on the oral cell methylome of healthy young vapers and smokers relative to non-users. Whereas vapers and smokers differ in number of differentially methylated regions (DMRs) (831 vs 2,863), they share striking similarities in the distribution and patterns of DNA methylation, chromatin states, transcription factor binding motifs, and pathways. There is substantial overlap in DMR-associated genes between vapers and smokers, with the shared subset of genes enriched for transcriptional regulation, signaling, tobacco use disorders, and cancer-related pathways. Of significance is the identification of a common hypermethylated DMR at the promoter of "Hypermethylated In Cancer 1" (HIC1), a tumor suppressor gene frequently silenced in smoking-related cancers. Our data support a potential link between epigenomic dysregulation in youth vapers and disease risk. These novel findings have significant implications for public health and tobacco product regulation.

青少年吸食者表观基因组失调:对疾病风险评估的影响。
尽管青少年吸食电子烟正在流行,但使用电子烟的长期健康后果在很大程度上还不为人所知。我们报告了吸烟与吸电子烟对健康年轻吸电子烟者和吸烟者口腔细胞甲基组的影响。虽然吸食者和吸烟者在差异甲基化区域(DMRs)的数量(831 对 2863)上存在差异,但他们在 DNA 甲基化的分布和模式、染色质状态、转录因子结合基序和途径方面却有着惊人的相似之处。吸食者和吸烟者的 DMR 相关基因有大量重叠,共同的基因子集富含转录调控、信号转导、烟草使用障碍和癌症相关途径。值得注意的是,在 "HIC1"(Hypermethylated In Cancer 1)的启动子上发现了一个共同的高甲基化 DMR,HIC1 是一种肿瘤抑制基因,在与吸烟有关的癌症中经常被沉默。我们的数据支持青少年吸食者表观基因组失调与疾病风险之间的潜在联系。这些新发现对公共卫生和烟草产品监管具有重要意义。
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来源期刊
CiteScore
11.20
自引率
3.10%
发文量
370
审稿时长
3-8 weeks
期刊介绍: The American Journal of Respiratory Cell and Molecular Biology publishes papers that report significant and original observations in the area of pulmonary biology. The focus of the Journal includes, but is not limited to, cellular, biochemical, molecular, developmental, genetic, and immunologic studies of lung cells and molecules.
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