AI Article Synopsis

  • Cigarette smoke exposure influences DNA methylation, particularly increasing methylation at enhancers in lung tissue over time, while having less impact on liver tissue.
  • The study used advanced sequencing techniques to analyze these effects in genetically modified mice over eight months of exposure.
  • Importantly, stopping smoking or switching to a less harmful tobacco product (THS 2.2) significantly reduced these methylation changes, indicating that the epigenetic effects of cigarette smoke can be reversed.

Article Abstract

Cigarette smoke (CS) exposure has been shown to correlate with changes in DNA methylation levels, however, the impact of CS on DNA methylation at genome-wide scale is missing. Here, we used whole-genome bisulfite sequencing to assess the effects of CS extract and aerosol from the Tobacco Heating System (THS) 2.2, a candidate modified risk tobacco product, on DNA methylation in lung and liver tissues from apolipoprotein E-deficient mice during an eight-month period of exposure. We found that in lung tissue, CS mainly induced hypermethylation of candidate enhancers at late time points, while promoters were less affected. This effect was strongly reduced upon cessation or switching to THS 2.2. By contrast, chronic exposure to THS 2.2 had a limited effect on DNA methylation at both promoters and enhancers. We also identified members of the Ets and Fox families of transcription factors as potential players in the epigenetic response to CS exposure in lung tissue. In contrast to the lung, DNA methylation in the liver was largely insensitive to all investigated exposures. In summary, our investigations indicate that CS-related DNA methylation alterations are tissue-specific, occur mainly at enhancers and are strongly reduced upon smoking cessation or switching to THS2.2.

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Source
http://dx.doi.org/10.1016/j.fct.2018.11.020DOI Listing

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