DNA methylation alterations in response to pesticide exposure in vitro.

Published

Journal Article

Although pesticides are subject to extensive carcinogenicity testing before regulatory approval, pesticide exposure has repeatedly been associated with various cancers. This suggests that pesticides may cause cancer via nonmutagenicity mechanisms. The present study provides evidence to support the hypothesis that pesticide-induced cancer may be mediated in part by epigenetic mechanisms. We examined whether exposure to seven commonly used pesticides (i.e., fonofos, parathion, terbufos, chlorpyrifos, diazinon, malathion, and phorate) induces DNA methylation alterations in vitro. We conducted genome-wide DNA methylation analyses on DNA samples obtained from the human hematopoietic K562 cell line exposed to ethanol (control) and several organophosphate pesticides (OPs) using the Illumina Infinium HumanMethylation27 BeadChip. Bayesian-adjusted t-tests were used to identify differentially methylated gene promoter CpG sites. In this report, we present our results on three pesticides (fonofos, parathion, and terbufos) that clustered together based on principle component analysis and hierarchical clustering. These three pesticides induced similar methylation changes in the promoter regions of 712 genes, while also exhibiting their own OP-specific methylation alterations. Functional analysis of methylation changes specific to each OP, or common to all three OPs, revealed that differential methylation was associated with numerous genes that are involved in carcinogenesis-related processes. Our results provide experimental evidence that pesticides may modify gene promoter DNA methylation levels, suggesting that epigenetic mechanisms may contribute to pesticide-induced carcinogenesis. Further studies in other cell types and human samples are required, as well as determining the impact of these methylation changes on gene expression.

Full Text

Duke Authors

Cited Authors

  • Zhang, X; Wallace, AD; Du, P; Kibbe, WA; Jafari, N; Xie, H; Lin, S; Baccarelli, A; Soares, MB; Hou, L

Published Date

  • August 2012

Published In

Volume / Issue

  • 53 / 7

Start / End Page

  • 542 - 549

PubMed ID

  • 22847954

Pubmed Central ID

  • 22847954

Electronic International Standard Serial Number (EISSN)

  • 1098-2280

Digital Object Identifier (DOI)

  • 10.1002/em.21718

Language

  • eng

Conference Location

  • United States