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World Trade Center Exposure, DNA Methylation Changes, and Cancer: A Review of Current Evidence.

Authors :
Tuminello, Stephanie
Nguyen, Emelie
Durmus, Nedim
Alptekin, Ramazan
Yilmaz, Muhammed
Crisanti, Maria Cecilia
Snuderl, Matija
Chen, Yu
Shao, Yongzhao
Reibman, Joan
Taioli, Emanuela
Arslan, Alan A.
Source :
Epigenomes; Dec2023, Vol. 7 Issue 4, p31, 12p
Publication Year :
2023

Abstract

Introduction: Known carcinogens in the dust and fumes from the destruction of the World Trade Center (WTC) towers on 9 November 2001 included metals, asbestos, and organic pollutants, which have been shown to modify epigenetic status. Epigenome-wide association analyses (EWAS) using uniform (Illumina) methodology have identified novel epigenetic profiles of WTC exposure. Methods: We reviewed all published data, comparing differentially methylated gene profiles identified in the prior EWAS studies of WTC exposure. This included DNA methylation changes in blood-derived DNA from cases of cancer-free "Survivors" and those with breast cancer, as well as tissue-derived DNA from "Responders" with prostate cancer. Emerging molecular pathways related to the observed DNA methylation changes in WTC-exposed groups were explored and summarized. Results: WTC dust exposure appears to be associated with DNA methylation changes across the genome. Notably, WTC dust exposure appears to be associated with increased global DNA methylation; direct dysregulation of cancer genes and pathways, including inflammation and immune system dysregulation; and endocrine system disruption, as well as disruption of cholesterol homeostasis and lipid metabolism. Conclusion: WTC dust exposure appears to be associated with biologically meaningful DNA methylation changes, with implications for carcinogenesis and development of other chronic diseases. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20754655
Volume :
7
Issue :
4
Database :
Complementary Index
Journal :
Epigenomes
Publication Type :
Academic Journal
Accession number :
174440577
Full Text :
https://doi.org/10.3390/epigenomes7040031