Tobacco exposure-related alterations in DNA methylation and gene expression in human monocytes: the Multi-Ethnic Study of Atherosclerosis (MESA)

Lindsay M. Reynolds, Kurt Lohman, Gary S. Pittman, R. Graham Barr, Gloria C. Chi, Joel Kaufman, Ma Wan, Douglas A. Bell, Michael J. Blaha, Carlos J. Rodriguez, Yongmei Liu

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

Abstract

Alterations in DNA methylation and gene expression in blood leukocytes are potential biomarkers of harm and mediators of the deleterious effects of tobacco exposure. However, methodological issues, including the use of self-reported smoking status and mixed cell types have made previously identified alterations in DNA methylation and gene expression difficult to interpret. In this study, we examined associations of tobacco exposure with DNA methylation and gene expression, utilizing a biomarker of tobacco exposure (urine cotinine) and CD14+ purified monocyte samples from 934 participants of the community-based Multi-Ethnic Study of Atherosclerosis (MESA). Urine cotinine levels were measured using an immunoassay. DNA methylation and gene expression were measured with microarrays. Multivariate linear regression was used to test for associations adjusting for age, sex, race/ethnicity, education, and study site. Urine cotinine levels were associated with methylation of 176 CpGs [false discovery rate (FDR)<0.01]. Four CpGs not previously identified by studies of non-purified blood samples nominally replicated (P value<0.05) with plasma cotinine-associated methylation in 128 independent monocyte samples. Urine cotinine levels associated with expression of 12 genes (FDR<0.01), including increased expression of P2RY6 (Beta ± standard error = 0.078 ± 0.008, P = 1.99 × 10−22), a gene previously identified to be involved in the release of pro-inflammatory cytokines. No cotinine-associated (FDR<0.01) methylation profiles significantly (FDR<0.01) correlated with cotinine-associated (FDR<0.01) gene expression profiles. In conclusion, our findings i) identify potential monocyte-specific smoking-associated methylation patterns and ii) suggest that alterations in methylation may not be a main mechanism regulating gene expression in monocytes in response to cigarette smoking.

Original languageEnglish (US)
Pages (from-to)1092-1100
Number of pages9
JournalEpigenetics
Volume12
Issue number12
DOIs
StatePublished - Dec 2 2017
Externally publishedYes

Keywords

  • CD14+ monocyte
  • Cigarette
  • DNA methylation
  • cotinine
  • gene expression
  • smoking
  • tobacco

ASJC Scopus subject areas

  • Molecular Biology
  • Cancer Research

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