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DNA fragmentation in human fibroblasts under extremely low frequency electromagnetic field exposure
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 110567
Author(s) Focke, Frauke; Schuermann, David; Kuster, Niels; Schär, Primo
Author(s) at UniBasel Schär, Primo Leo
Year 2010
Title DNA fragmentation in human fibroblasts under extremely low frequency electromagnetic field exposure
Journal Mutation research
Volume 683
Number 1-2
Pages / Article-Number 74-83
Keywords Electromagnetic fields, Genotoxicity, Comet assay, Human cells, Cell cycle, Apoptosis
Abstract

Extremely low frequency electromagnetic fields (ELF-EMFs) were reported to affect DNA integrity in human cells with evidence based on the Comet assay. These findings were heavily debated for two main reasons; the lack of reproducibility, and the absence of a plausible scientific rationale for how EMFs could damage DNA. Starting out from a replication of the relevant experiments, we performed this study to clarify the existence and explore origin and nature of ELF-EMF induced DNA effects. Our data confirm that intermittent (but not continuous) exposure of human primary fibroblasts to a 50Hz EMF at a flux density of 1mT induces a slight but significant increase of DNA fragmentation in the Comet assay, and we provide first evidence for this to be caused by the magnetic rather than the electric field. Moreover, we show that EMF-induced responses in the Comet assay are dependent on cell proliferation, suggesting that processes of DNA replication rather than the DNA itself may be affected. Consistently, the Comet effects correlated with a reduction of actively replicating cells and a concomitant increase of apoptotic cells in exposed cultures, whereas a combined Fpg-Comet test failed to produce evidence for a notable contribution of oxidative DNA base damage. Hence, ELF-EMF induced effects in the Comet assay are reproducible under specific conditions and can be explained by minor disturbances in S-phase processes and occasional triggering of apoptosis rather than by the generation of DNA damage.

Publisher Elsevier Science
ISSN/ISBN 0027-5107
edoc-URL http://edoc.unibas.ch/dok/A5253989
Full Text on edoc No
Digital Object Identifier DOI 10.1016/j.mrfmmm.2009.10.012
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/19896957
ISI-Number WOS:000273845500011
Document type (ISI) Journal Article
 
   

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