2008
DOI: 10.1016/j.mrrev.2008.03.007
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The micronucleus assay in human buccal cells as a tool for biomonitoring DNA damage: The HUMN project perspective on current status and knowledge gaps

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Cited by 508 publications
(479 citation statements)
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“…Bio-monitoring the effect of exposure to genotoxic substances in the workplace is essential for the development of strategies to improve occupational health and safety conditions [9]. Human bio-monitoring may be done with various cytogenetic tests that evaluate genotoxic effects by detecting DNA damage, such as sister chromatid exchange and micronuclei [10,11]. Micronuclei in exfoliated buccal epithelial cells emerge during mitosis of the basal layers of the epithelium as extra-chromosomal DNA particles, when chromosome fragments or whole chromosomes lag behind and fail to be included in the main nuclei of the daughter cells, as a result of a clastogenic or aneugenic events [11,12].…”
Section: Introductionmentioning
confidence: 99%
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“…Bio-monitoring the effect of exposure to genotoxic substances in the workplace is essential for the development of strategies to improve occupational health and safety conditions [9]. Human bio-monitoring may be done with various cytogenetic tests that evaluate genotoxic effects by detecting DNA damage, such as sister chromatid exchange and micronuclei [10,11]. Micronuclei in exfoliated buccal epithelial cells emerge during mitosis of the basal layers of the epithelium as extra-chromosomal DNA particles, when chromosome fragments or whole chromosomes lag behind and fail to be included in the main nuclei of the daughter cells, as a result of a clastogenic or aneugenic events [11,12].…”
Section: Introductionmentioning
confidence: 99%
“…Human bio-monitoring may be done with various cytogenetic tests that evaluate genotoxic effects by detecting DNA damage, such as sister chromatid exchange and micronuclei [10,11]. Micronuclei in exfoliated buccal epithelial cells emerge during mitosis of the basal layers of the epithelium as extra-chromosomal DNA particles, when chromosome fragments or whole chromosomes lag behind and fail to be included in the main nuclei of the daughter cells, as a result of a clastogenic or aneugenic events [11,12]. Micronuclei in epithelial cells reflect genotoxic events occurring in the dividing basal cell layer of the putative target organ 1-3 weeks earlier [13,14], which allows for cytogenetic surveillance of groups at high risk of developing organ-specific cancer (e.g., upper aerodigestive tract) or oral premalignant lesions [15][16][17].…”
Section: Introductionmentioning
confidence: 99%
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