Inorganic arsenic is methylated in the mammalian body to methylarsonic acid (MMA), dimethylarsinic acid (DMA) and trimethylarsine oxide (TMA). To achieve a more precise understanding of arsenic carcinogenicity, we examined the genotoxic effects of organic arsenic compounds on human lymphocytes by as
Cell cycle dependent aneuploidy induction by x-rays in vitro in human lymphocytes
β Scribed by Tallon, I.; Verschaeve, L.; Kirsch-Volders, M.
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 152 KB
- Volume
- 40
- Category
- Article
- ISSN
- 1059-910X
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β¦ Synopsis
Although ionising radiation mainly induces DNA strand breaks leading to chromosomal aberrations, there are indications that it also might induce numerical chromosome aberrations (aneuploidy). The existing data, however, do not provide evidence for a mechanism. To assess the relative sensitivity of the G 1 vs. G 2 cellular targets, whole blood cultures of lymphocytes were irradiated in vitro with different doses of X-rays (0.5, 1 and 2 Gy). The lymphocytes were harvested after cytochalasin-B blockade to allow the selective study of binucleated cells, having undergone only one division in culture. Harvesting was performed at different sampling times (70, 74, and 78 hours). To evaluate the micronuclei, regarding whole chromosomes or acentric fragments, an oligonucleotide probe that recognises the centromeric region of all human chromosomes was used. The relative percentage of centromere-positive micronuclei ranged from 5 up to 18% depending on the cell cycle stage and on the received dose. Cells exposed during the G 1 phase exhibited a slightly higher frequency of centromere-positive micronuclei than cells that were in G 2 at the time of exposure. G 1 exposure induced a centromere-positive micronuclei dose-effect relationship that was not observed after G 2 exposure. The observed difference in response of both phases on the centromere-positive micronuclei yields may be due to the involvement of different targets. Microsc.
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