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Integrated analysis of multi-omics data on epigenetic changes caused by combined exposure to environmental hazards

Authors
Yu, So YeonKoh, Eun JungKim, Seung HwanLee, So YulLee, Ji SuSon, Sang WookHwang, Seung Yong
Issue Date
Jun-2021
Publisher
WILEY
Keywords
combined exposure; epigenetic; long noncoding RNA; long-term depression; synapse
Citation
ENVIRONMENTAL TOXICOLOGY, v.36, no.6, pp.1001 - 1010
Indexed
SCIE
SCOPUS
Journal Title
ENVIRONMENTAL TOXICOLOGY
Volume
36
Number
6
Start Page
1001
End Page
1010
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/144677
DOI
10.1002/tox.23099
ISSN
1520-4081
Abstract
Humans are easily exposed to environmentally hazardous factors in industrial sites or daily life. In addition, exposure to various substances and not just one harmful substance is common. However, research on the effects of combined exposure on humans is limited. Therefore, this study examined the effects of combined exposure to volatile organic compounds (VOCs) on the human body. We separated 193 participants into four groups according to their work-related exposure (nonexposure, toluene exposure, toluene and xylene exposure, and toluene, ethylbenzene, and xylene exposure). We then identified the methylation level and long noncoding RNA (lncRNA) levels by omics analyses, and performed an integrated analysis to examine the change of gene expression. Thereafter, the effects of combined exposure to environmental hazards on the human body were investigated and analyzed. Exposure to VOCs was found to negatively affect the development and maintenance of the nervous system. In particular, the MALAT1 lncRNA was found to be significantly reduced in the complex exposure group, and eight genes were significantly downregulated by DNA hypermethylation. The downregulation of these genes could cause a possible decrease in the density of synapses as well as the number and density of dendrites and spines. In summary, we found that increased combined exposure to environmental hazards could lead to additional epigenetic changes, and consequently abnormal dendrites, spines, and synapses, which could damage motor learning or spatial memory. Thus, lncRNA MALAT1 or FMR1 could be novel biomarkers of neurotoxicity to identify the negative health effects of VOC complex exposure.
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