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Title: The association between personal sun exposure, serum vitamin D and global methylation in human lymphocytes in a population of healthy adults in South Australia
Authors: Nair-Shalliker, V
Dhillon, V
Clements, M
Armstrong, BK
Fenech, M
Categories: Cancer Type - Skin Cancer
Causes & Exposures - Prevention & Education
Causes & Exposures - Genes
Causes & Exposures - UV/Sun Exposure
Population Groups - Australia
Pub. Date: Jul-2014
Journal Title: Mutation Research [Mutat Res]
Volume: 765
Page number start: 6
Page number end: 10
Citation: 765: 6-10
Abstract: BACKGROUND: There is a positive association between solar UV exposure and micronucleus frequency in peripheral blood lymphocytes (PBL) and this association may be stronger when serum vitamin D (25(OH)D) levels are insufficient (<50 nmol/L). Micronucleus formation can result from global hypomethylation of DNA repeat sequences. The aim of this analysis was to evaluate the relationship between solar UV exposure and methylation pattern in LINE-1 repetitive elements in PBL DNA and to see if serum 25(OH)D levels modify it. METHOD: Personal solar UV exposure was estimated from hours of outdoor exposure over 6 weeks recalled at the time of blood collection in 208 male and female participants living in South Australia. Methylation in LINE-1 repetitive elements was assessed in PBL using pyrosequencing. RESULTS: Methylation in LINE-1 decreased with increasing solar UV exposure (% decrease = 0.5% per doubling of sUV; 95%CI: -0.7 to -0.2 p(value) = 0.00003). Although there was no correlation between LINE-1 methylation and micronucleus frequency, there was a 4.3% increase (95%CI: 0.6-8.1 p-value = 0.02) in nucleoplasmic bridges and a 4.3% increase in necrosis (CI: 1.9-6.8 p-value = 0.0005) for every 1% increase in LINE-1 methylation. Serum 25(OH)D was not associated with DNA methylation; or did it modify the association of solar UV with DNA methylation. CONCLUSION: Exposure to solar UV radiation may reduce DNA methylation in circulating lymphocytes. This association does not appear to be influenced or mediated by vitamin D status.
Division: Cancer Research Division
DOI: 10.1016/j.mrfmmm.2014.04.001
URI: http://researchpubs.cancercouncil.com.au/cancercounciljspui/handle/1/1695
Appears in Collections:Research Articles

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