4.7 Article

Lung mitochondrial DNA copy number, inflammatory biomarkers, gene transcription and gene methylation in vapers and smokers

期刊

EBIOMEDICINE
卷 85, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.ebiom.2022.104301

关键词

Mitochondria copy numbers; Smokers; Vaping; DNA methylation; Gene expression; Inflammation

资金

  1. National Cancer Institute of the National Institutes of Health (NIH) [P30 CA016058]
  2. Food and Drug Administration Center for Tobacco Products (CTP) [P50CA180908]
  3. National Heart, Lung, and Blood Institute [R21HL147401]
  4. National Center For Advancing Translational Sciences [UL1TR001070]
  5. Pelotonia Intramural Research Funds
  6. Prevent Cancer Foundation

向作者/读者索取更多资源

This study found that smoking may cause lung toxic effects through mitochondrial DNA copy number (mtCN). While the impact of electronic cigarettes (EC) is less clear, the presence of EC-specific associations of mtCN with nuclear biomarkers suggests that exposure may not be harmless. Further research is needed to understand the role of smoking and EC-related mtCN in lung disease risks.
Background Mitochondrial DNA copy number (mtCN) maintains cellular function and homeostasis, and is linked to nudear DNA methylation and gene expression. Increased mtCN in the blood is associated with smoking and respiratory disease, but has received little attention for target organ effects for smoking or electronic cigarette (EC) use. Methods Bronchoscopy biospecimens from healthy EC users, smokers (SM), and never-smokers (NS) were assessed for associations of mtCN with mtDNA point mutations, immune responses, nuclear DNA methylation and gene expression using linear regression. Ingenuity pathway analysis was used for enriched pathways. GEO and TCGA respiratory disease datasets were used to explore the involvement of mtCN-associated signatures. Findings mtCN was higher in SM than NS, but EC was not statistically different from either. Overall there was a negative association of mtCN with a point mutation in the D-loop but no difference within groups. Positive associations of mtCN with IL-2 and IL-4 were found in EC only. mtCN was significantly associated with 71,487 CpGs and 321 transcripts. 263 CpGs were correlated with nearby transcripts for genes enriched in the immune system. EC-specific mtCN-associated-CpGs and genes were differentially expressed in respiratory diseases compared to controls, including genes involved in cellular movement, inflammation, metabolism, and airway hyperresponsiveness. Interpretation Smoking may elicit a lung toxic effect through mtCN. While the impact of EC is less clear, EC-specific associations of mtCN with nuclear biomarkers suggest exposure may not be harmless. Further research is needed to understand the role of smoking and EC-related mtCN on lung disease risks. Copyright (C) 2022 The Author(s). Published by Elsevier B.V.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据