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https://hdl.handle.net/2440/54727
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dc.contributor.author | Wu, J. | - |
dc.contributor.author | Lyons, G. | - |
dc.contributor.author | Graham, R. | - |
dc.contributor.author | Fenech, M. | - |
dc.date.issued | 2009 | - |
dc.identifier.citation | Mutagenesis, 2009; 24(3):225-232 | - |
dc.identifier.issn | 0267-8357 | - |
dc.identifier.issn | 1464-3804 | - |
dc.identifier.uri | http://hdl.handle.net/2440/54727 | - |
dc.description | © The Author 2009. Published by Oxford University Press on behalf of the UK Environmental Mutagen Society. All rights reserved. | - |
dc.description.abstract | A supranutritional intake of selenium (Se) may be required for cancer prevention, but an excessively high dose could be toxic. Therefore, the effect on genome stability of seleno-L-methionine (Se-met), the most important dietary form of Se, was measured to determine its bioefficacy and safety limit. Peripheral blood lymphocytes were isolated from six volunteers and cultured with medium supplemented with Se-met in a series of Se concentrations (3, 31, 125, 430, 1880 and 3850 µg Se/litre) while keeping the total methionine (i.e. Se-met + L-methionine) concentration constant at 50 µM. Baseline genome stability of lymphocytes and the extent of DNA damage induced by 1.5-Gy -ray were investigated using the cytokinesis-block micronucleus cytome assay after 9 days of culture in 96-microwell plates. High Se concentrations (1880 µg Se/litre) caused strong inhibition of cell division and increased cell death (P < 0.0001). Baseline frequency of nucleoplasmic bridges and nuclear buds, however, declined significantly (P trend < 0.05) as Se concentration increased from 3 to 430 µg Se/litre. Se concentration (430 µg Se/litre) had no significant effect on baseline frequency of micronuclei and had no protective effect against genome damage induced by exposure to 1.5-Gy -ray irradiation. In conclusion, Se, as Se-met, may improve genome stability at concentrations up to 430 µg Se/litre, but higher doses may be cytotoxic. Therefore, a cautious approach to supplementation with Se-met is required to ensure that optimal genome health is achieved without cytotoxic effects. | - |
dc.description.statementofresponsibility | Jing Wu, Graham H. Lyons, Robin D. Graham and Michael F. Fenech | - |
dc.language.iso | en | - |
dc.publisher | Oxford Univ Press | - |
dc.source.uri | http://dx.doi.org/10.1093/mutage/gen074 | - |
dc.subject | Lymphocytes | - |
dc.subject | Humans | - |
dc.subject | Neoplasms | - |
dc.subject | DNA Damage | - |
dc.subject | Genomic Instability | - |
dc.subject | Selenomethionine | - |
dc.subject | Micronucleus Tests | - |
dc.subject | Cell Death | - |
dc.subject | Dose-Response Relationship, Drug | - |
dc.subject | Gamma Rays | - |
dc.subject | Adult | - |
dc.subject | Middle Aged | - |
dc.subject | Male | - |
dc.subject | Mass Spectrometry | - |
dc.title | The effect of selenium, as selenomethionine, on genome stability and cytotoxicity in human lymphocytes measured using the cytokinesis-block micronucleus cytome assay | - |
dc.type | Journal article | - |
dc.identifier.doi | 10.1093/mutage/gen074 | - |
pubs.publication-status | Published | - |
dc.identifier.orcid | Fenech, M. [0000-0002-8466-0991] | - |
Appears in Collections: | Agriculture, Food and Wine publications Aurora harvest 5 |
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