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Article

Changes in DNA methylation induced by multi-walled carbon nanotube exposure in the workplace

ORCID Icon, , , , ORCID Icon, , , , ORCID Icon, , ORCID Icon & show all
Pages 1195-1210 | Received 01 Jun 2017, Accepted 13 Nov 2017, Published online: 30 Nov 2017
 

Abstract

This study was designed to assess the epigenetic alterations in blood cells, induced by occupational exposure to multi-wall carbon nanotubes (MWCNT). The study population comprised of MWCNT-exposed workers (n=24) and unexposed controls (n=43) from the same workplace. We measured global DNA methylation/hydroxymethylation levels on the 5th cytosine residues using a validated liquid chromatography tandem-mass spectrometry (LC-MS/MS) method. Sequence-specific methylation of LINE1 retrotransposable element 1 (L1RE1) elements, and promoter regions of functionally important genes associated with epigenetic regulation [DNA methyltransferase-1 (DNMT1) and histone deacetylase 4 (HDAC4)], DNA damage/repair and cell cycle pathways [nuclear protein, coactivator of histone transcription/ATM serine/threonine kinase (NPAT/ATM)], and a potential transforming growth factor beta (TGF-β) repressor [SKI proto-oncogene (SKI)] were studied using bisulfite pyrosequencing. Analysis of global DNA methylation levels and hydroxymethylation did not reveal significant difference between the MWCNT-exposed and control groups. No significant changes in Cytosine-phosphate-Guanine (CpG) site methylation were observed for the LINE1 (L1RE1) elements. Further analysis of gene-specific DNA methylation showed a significant change in methylation for DNMT1, ATM, SKI, and HDAC4 promoter CpGs in MWCNT-exposed workers. Since DNA methylation plays an important role in silencing/regulation of the genes, and many of these genes have been associated with occupational and smoking-induced diseases and cancer (risk), aberrant methylation of these genes might have a potential effect in MWCNT-exposed workers.

Disclosure statement

The authors do not have any conflict of interest.

Additional information

Funding

Manosij Ghosh is the recipient of a European Respiratory Society RESPIRE postdoctoral fellowship (RESPIRE2 – 2014–7310). DÖ would like to acknowledge financial assistance to Stichting Tegen Kanker (agreement no: 2012–218, project no: 3M150270).

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