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首页> 外文期刊>Toxicology in vitro: an international journal published in association with BIBRA >9,10-Phenanthrenequinone induces DNA deletions and forward mutations via oxidative mechanisms in the yeast Saccharomyces cerevisiae.
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9,10-Phenanthrenequinone induces DNA deletions and forward mutations via oxidative mechanisms in the yeast Saccharomyces cerevisiae.

机译:9,10-菲醌通过酿酒酵母中的氧化机制诱导DNA缺失和正向突变。

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摘要

The estimated cancer risk from diesel exhaust particles (DEP) in the air is approximately 70% of the cancer risk from all air pollutants. DEP is comprised of a complex mixture of chemicals whose carcinogenic potential has not been adequately assessed. The polycyclic aromatic hydrocarbon quinone 9,10-phenanthrenequinone (9,10 PQ) is a major component of DEP and a suspect genotoxic agent for DEP induced DNA damage. 9,10 PQ undergoes redox cycling to produce reactive oxygen species that can lead to oxidative DNA damage. We used two systems in the yeast Saccharomyces cerevisiae to examine possible differential genotoxicity of 9,10 PQ. The DEL assay measures intra-chromosomal homologous recombination leading to DNA deletions and the CAN assay measures forward mutations leading to canavanine resistance. Cells were exposed to 9,10 PQ aerobically and anaerobically followed by DNA damage assessment. The results indicate that 9,10 PQ induces DNA deletions and point mutations in the presence of oxygen while exhibiting negligible effects anaerobically. In contrast to the cytotoxicity observed aerobically, the anaerobic effects of 9,10 PQ seem to be cytostatic in nature, reducing growth without affecting cell viability. Thus, 9,10 PQ requires oxygen for genotoxicity while different toxicities exhibited aerobically and anaerobically suggest multiple mechanisms of action.
机译:估计空气中柴油机废气颗粒(DEP)引起的癌症风险约为所有空气污染物引起的癌症风险的70%。 DEP由化学物质的复杂混合物组成,其致癌潜力尚未得到充分评估。多环芳烃醌9,10-菲醌(9,10 PQ)是DEP的主要成分,也是DEP诱导的DNA损伤的潜在遗传毒性剂。 9,10 PQ经历氧化还原循环,产生活性氧,可能导致DNA氧化损伤。我们在啤酒酵母中使用了两种系统来检查9,10 PQ的可能的不同基因毒性。 DEL测定可测量导致DNA缺失的染色体内同源重组,而CAN测定则可测量导致卡那万碱抗性的正向突变。细胞需氧和厌氧暴露于9,10 PQ,然后进行DNA损伤评估。结果表明,9,10 PQ在有氧条件下诱导DNA缺失和点突变,而厌氧性表现可忽略不计。与需氧观察到的细胞毒性相反,9,10 PQ的厌氧作用似乎具有抑制细胞生长的作用,从而在不影响细胞活力的情况下减少了生长。因此,9,10 PQ的遗传毒性需要氧气,而需氧和厌氧的不同毒性表明存在多种作用机理。

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