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Methylation alterations at imprinted genes detected among long-term shiftworkers
Daniel I Jacobs1, Johnni Hansen, Alan Fu
1Department of Environmental Health Sciences, Yale School of Public Health, New Haven, Connecticut 06520, USA.
Long-term shiftwork may alter DNA methylation patterns in imprinted genes, potentially increasing cancer risk. This study found significant methylation changes in genes like DLX5, IGF2AS, and TP73 in female shiftworkers.
Area of Science:
- Epigenetics
- Occupational Health
- Cancer Research
Background:
- Shiftwork, involving light exposure at night, is associated with altered DNA methylation and increased cancer risk.
- Imprinted genes play crucial roles in development and disease, and their methylation patterns are tightly regulated.
Purpose of the Study:
- To investigate whether long-term shiftwork is associated with alterations in DNA methylation patterns at imprinted genes.
- To identify specific imprinted genes whose methylation may be affected by shiftwork.
Main Methods:
- Analysis of DNA methylation levels at 397 CpG sites in 56 imprinted genes using Illumina Infinium Methylation Assay.
- Comparison of methylation patterns between 10 female long-term shiftworkers and 10 age- and folate intake-matched female day workers.
- Quantitative DNA methylation analysis to confirm findings.
Main Results:
- Significant alterations in DNA methylation were observed in shiftworkers compared to day workers.
- Methylation was significantly higher at 20 CpG sites and lower at 30 CpG sites (P < 0.05).
- Strongest evidence for altered methylation was found for DLX5, IGF2AS, and TP73.
Conclusions:
- Long-term shiftwork may induce epigenetic changes, specifically altering methylation patterns at imprinted genes.
- These methylation alterations may represent a mechanism contributing to the carcinogenic potential of shiftwork.
- Further research is warranted to elucidate the role of shiftwork-induced epigenetic modifications in cancer development.
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