Cited by 34Epigenetics and DNA MethylationGenetic Syndromes and ImprintingSleep and Work-Related Fatigue

Methylation alterations at imprinted genes detected among long‐term shiftworkers

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Jacobs, Daniel I., Hansen, Johnni, Fu, Alan, Stevens, Richard G., Tjonneland, Anne, Vogel, Ulla B., Zheng, Tongzhang, Zhu, Yong·2013·Environmental and Molecular Mutagenesis

Abstract

Exposure to light at night through shiftwork has been linked to alterations in DNA methylation and increased risk of cancer development. Using an Illumina Infinium Methylation Assay, we analyzed methylation levels of 397 CpG sites in the promoter regions of 56 normally imprinted genes to investigate whether shiftwork is associated with alteration of methylation patterns. Methylation was significantly higher at 20 CpG sites and significantly lower at 30 CpG sites (P < 0.05) in 10 female long‐term shiftworkers as compared to 10 female age‐ and folate intake‐matched day workers. The strongest evidence for altered methylation patterns in shiftworkers was observed for DLX5, IGF2AS, and TP73 based on the magnitude of methylation change and consistency in the direction of change across multiple CpG sites, and consistent results were observed using quantitative DNA methylation analysis. We conclude that long‐term shiftwork may alter methylation patterns at imprinted genes, which may be an important mechanism by which shiftwork has carcinogenic potential and warrants further investigation. Environ. Mol. Mutagen., 2013. © 2012 Wiley Periodicals, Inc.

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  • Hypermethylation of MGMT has been reported to decrease apoptotic responses to DNA damage by TP73 and cell proliferation regulation by RBBP7, which in combination with aberrant expression of HOXA10, increase susceptibility for endometriosis.

    “The hypermethylation of methyltransferase (MGMT) has been reported to decrease apoptotic responses to DNA damage by TP73 and cell proliferation regulation by RBBP7, which in combination with the aberrant expression of HOXA10, increase the susceptibility for endometriosis.12,[41][42][43][44][45][46][47][48]”

    From Altered genome-wide methylation in endometriosis (2014) · cites this paper as [42]

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Authors
Jacobs, D. I., Hansen, J., Fu, A., Stevens, R. G., Tjonneland, A., Vogel, U. B., Zheng, T., & Zhu, Y.
Affiliations
  • Yale University (US)
  • Danish Cancer Society (DK)
  • UConn Health (US)
  • National Research Centre for the Working Environment (DK)
Corresponding author
Zhu, Yong
Venue
Environmental and Molecular Mutagenesis
Publisher
Wiley
Published
2012-11-28
Volume
54
Issue
2
Pages
141-146
ISSN
  • 0893-6692 (ISSN-L)
  • 1098-2280
OpenAlex
W2094158947
Cited by
34
References
30
Citations by year
2026: 2 · 2025: 2 · 2022: 1 · 2020: 2 · 2019: 1 · 2017: 8 · 2016: 2 · 2015: 7 · 2014: 5 · 2013: 4
FWCI
2.06
Type
journal article
Language
en
Open access
Locations
  • Environmental and Molecular Mutagenesis (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Institute of Environmental Health Sciences (ES018915, R21ES018915)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Syndromes and Imprinting
  • Social Sciences › Psychology › Experimental and Cognitive Psychology › Sleep and Work-Related Fatigue
Keywords
shift work, DNA methylation, genomic imprinting, imprinted genes, light at night, Dlx5, p73, promoter methylation, CpG sites, cancer risk
MeSH terms
Tumor Protein p73, DNA-Binding Proteins, Female, Humans, Light, Middle Aged, Neoplasms, Nuclear Proteins, Promoter Regions, Genetic, Proteins, Surveys and Questionnaires, Risk, Time Factors, Transcription Factors, Work Schedule Tolerance, Genomic Imprinting, Homeodomain Proteins, CpG Islands, DNA Methylation, Tumor Suppressor Proteins, Transcriptome

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