Micronuclei in humans induced by exposure to low level of ionizing radiation: influence of polymorphisms in DNA repair genes
Creators
- 1. Department of Pharmacology, University of Bologna, Via Irnerio 48, Bologna 40126 (Italy) and Department of Biosciences, Karolinska Institute, Novum, Huddinge 141 57 (Sweden)
- 2. Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Heidelberg (Germany)
- 3. Department of Biosciences, Karolinska Institute, Novum, Huddinge 141 57 (Sweden)
- 4. Department of Pharmacology, University of Bologna, Via Irnerio 48, Bologna 40126 (Italy)
- 5. Occupational Medicine Unit, S. Orsola-Malpighi Hospital, Via Pelagi 9, Bologna 40100 (Italy)
Description
Understanding the risks deriving from protracted exposure to low doses of ionizing radiation has remarkable societal importance in view of the large number of work settings in which sources of IR are encountered. To address this question, we studied the frequency of micronuclei (MN), which is an indicator of DNA damage, in a population exposed to low levels of ionizing radiation and in matched controls. In both exposed population and controls, the possible influence of single nucleotide polymorphisms in XRCC1, XRCC3 and XPD genes on the frequency of micronuclei was also evaluated. We also considered the effects of confounding factors, like smoking status, age and gender. The results indicated that MN frequency was significantly higher in the exposed workers than in the controls [8.62 ± 2.80 versus 6.86 ± 2.65; P = 0.019]. Radiological workers with variant alleles for XRCC1 or XRCC3 polymorphisms or wild-type alleles for XPD exon 23 or 10 polymorphisms showed a significantly higher MN frequency than controls with the same genotypes. Smoking status did not affect micronuclei frequency either in exposed workers or controls, while age was associated with increased MN frequency in the exposed only. In the combined population, gender but not age exerted an influence on the yield of MN, being higher in females than in males. Even though there is a limitation in this study due to the small number of subjects, these results suggest that even exposures to low level of ionizing radiation could have genotoxic effects and that XRCC3, XRCC1 and XPD polymorphisms might contribute to the increased genetic damage in susceptible individuals occupationally exposed to chronic low levels of ionizing radiation. For a clear conclusion on the induction of DNA damage caused by protracted exposure to low doses of ionizing radiation and the possible influence of genetic polymorphism in DNA repair genes larger studies are needed
Additional details
Identifiers
- DOI
- 10.1016/j.mrfmmm.2004.10.007;
- PII
- S0027-5107(04)00445-2;
Publishing Information
- Journal Title
- Mutation Research
- Journal Volume
- 570
- Journal Issue
- 1
- Journal Page Range
- p. 105-117
- ISSN
- 0027-5107
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 36061831
- Subject category
- S63: RADIATION, THERMAL, AND OTHER ENVIRONMENTAL POLLUTANT EFFECTS ON LIVING ORGANISMS AND BIOLOGICAL MATERIALS; S61: RADIATION PROTECTION AND DOSIMETRY;
- Descriptors DEI
- CHROMOSOMAL ABERRATIONS; CONTROL; DNA DAMAGES; DOSE EQUIVALENTS; EXCISION REPAIR; FLUORESCENCE; GENES; IN-SITU HYBRIDIZATION; IONIZING RADIATIONS; NEOPLASMS; NUCLEOTIDES; NUTRITION; OCCUPATIONAL EXPOSURE; POLYMERASE CHAIN REACTION; RADIATION DOSES; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- BIOLOGICAL RECOVERY; BIOLOGICAL REPAIR; BIOTECHNOLOGY; COHERENT SCATTERING; DIFFRACTION; DISEASES; DNA REPAIR; DOSES; ELECTRON SPECTROSCOPY; EMISSION; GENE AMPLIFICATION; GENETIC ENGINEERING; LUMINESCENCE; MUTATIONS; NUCLEIC ACID HYBRIDIZATION; ORGANIC COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; PHOTON EMISSION; RADIATIONS; REPAIR; SCATTERING; SPECTROSCOPY
Optional Information
- Copyright
- Copyright (c) 2004 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.