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Synergistic genotoxic effect between gene and environmental pollutant: Oxidative DNA damage induced by thioredoxin reductase 1 silencing under nickel treatment

机译:基因与环境污染物之间的协同遗传毒性效应:镍处理下硫氧还蛋白还原酶1沉默导致的氧化性DNA损伤

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摘要

Nickel has been known to represent a lethal toxicity to human under environmental exposure. Particulary, nickel accumulation is able to cause oxidative DNA damage and tumor development. Redox imbalance by oxidative stress is rescued via modulation byredox factors which can scavenge excessively produced reactive oxygen species (ROS). Thioredoxin reductase 1 (Trr 1) is one of major redox factors having a potential role in cellular defense system against oxidative stress. In this study, we investigatedwhether Trr 1 has protective roles against nickel-induced oxida-l ive stress and genotoxicity using ROS measurement, comet and micronucleus (MN) assay. We found significant increase of intracellular ROS generation in nickel-treated Trr 1 defective cellscompared with Trr 1 proficient cells. In addition, under nickel treatment, Trr I knockdown cells showed higher amount of DNA strand breaks as oxidative DNA damage rather than in Trr 1 wild type cells. Moreover, MN as a crucial bio-marker for carcinogenicity was remarkably induced in the nickel-exposed Trr 1 silencing cells. Therefore, these results might provide novel insight on the role of Trr 1 in cellular protection from environmental nickel-induced genotoxicity. In conclusion, we emphasized the synergistic toxicity of Trr 1 knockdown and environmental nickel exposure in relevance to gene-environment interactions.
机译:已知镍在环境暴露下对人体具有致命毒性。特别地,镍的积累能够引起氧化性DNA损伤和肿瘤发展。通过氧化还原因子的调节可以挽救氧化应激引起的氧化还原不平衡,该氧化还原因子可以清除过量产生的活性氧(ROS)。硫氧还蛋白还原酶1(Trr 1)是主要的氧化还原因子之一,在细胞防御系统对抗氧化应激中具有潜在作用。在这项研究中,我们使用ROS测量,彗星和微核(MN)分析研究了Trr 1是否对镍诱导的氧化应激和遗传毒性具有保护作用。我们发现,与Trr 1精通细胞相比,镍处理的Trr 1缺陷细胞中细胞内ROS的产生显着增加。另外,在镍处理下,Trr I敲低的细胞显示出更高数量的DNA链断裂(作为氧化DNA损伤),而不是在Trr 1野生型细胞中。此外,MN是致癌性的重要生物标志物,在暴露于镍的Trr 1沉默细胞中被显着诱导。因此,这些结果可能提供有关Trr 1在细胞保护中免受环境镍诱导的基因毒性作用的新颖见解。总之,我们强调了与基因-环境相互作用相关的Trr 1基因敲低和环境镍暴露的协同毒性。

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