首页> 外文期刊>Teratogenesis, carcinogenesis, and mutagenesis >Detection of DNA strand breaks, DNA-protein crosslinks, and telomerase activity in nickel-transformed BALB/c-3T3 cells.
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Detection of DNA strand breaks, DNA-protein crosslinks, and telomerase activity in nickel-transformed BALB/c-3T3 cells.

机译:在镍转化的BALB / c-3T3细胞中检测DNA链断裂,DNA-蛋白质交联和端粒酶活性。

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摘要

Although nickel compounds are known carcinogens, the underlying carcinogenic mechanisms are not fully understood. The objective of this research was to determine if the genotoxic lesions of DNA strand breaks and DNA-protein crosslinks are present in nickel-transformed BALB/c-3T3 cells, and to further elucidate the potential carcinogenesis of insoluble and soluble nickel compounds through telomerase activity in nickel-transformed BALB/c-3T3 cell lines. DNA strand breaks, DNA-protein crosslinks and telomerase activity were investigated by single cell gel electrophoresis (comet assay), (125)I-postlabelling techniques, and the TRAP-silver staining assay, respectively. Results showed that both DNA strand breaks and DNA-protein crosslinks were present in nickel-transformed BALB/c-3T3 cells. However, the highest levels of DNA strand breaks and DNA-protein crosslinks were found in insoluble crystalline NiS-transformed cells and high levels of DNA strand breaks and DNA-protein crosslinks were also found in the transformed cells induced by two water-soluble NiCl(2) and NiSO(4) at moderate concentrations of cytotoxicity. These data suggest that these two genetic endpoints are useful biomarkers and are associated with cell transformation and carcinogensis of insoluble and soluble nickel compounds. Also, we found that the crystalline NiS- and NiCl(2)-transformed cells possessed a high telomerase activity. A weak telomerase was found in NiSO(4)-transformed cells. The results seem to indicate that in addition to crystalline NiS, some water-soluble nickel compounds such as NiCl(2) are also highly carcinogenic. These results may partly explain the cell transformation and relative carcinogenic potency of insoluble crystalline NiS, soluble NiCl(2), and NiSO(4). Copyright 2001 Wiley-Liss, Inc.
机译:尽管镍化合物是已知的致癌物,但潜在的致癌机理尚未完全明了。这项研究的目的是确定在镍转化的BALB / c-3T3细胞中是否存在DNA链断裂和DNA-蛋白质交联的遗传毒性损伤,并通过端粒酶活性进一步阐明不溶和可溶镍化合物的潜在致癌作用。在镍转化的BALB / c-3T3细胞系中。通过单细胞凝胶电泳(彗星试验),(125)I后标记技术和TRAP-银染色试验分别研究了DNA链断裂,DNA-蛋白质交联和端粒酶活性。结果表明,镍转化的BALB / c-3T3细胞中均存在DNA链断裂和DNA-蛋白质交联现象。然而,在不溶性结晶NiS转化的细胞中发现了最高水平的DNA链断裂和DNA-蛋白质交联,并且在由两种水溶性NiCl诱导的转化细胞中也发现了高水平的DNA链断裂和DNA-蛋白质交联。 2)和中等浓度的细胞毒性NiSO(4)。这些数据表明这两个遗传终点是有用的生物标记,并且与不溶和可溶镍化合物的细胞转化和致癌作用有关。此外,我们发现结晶NiS和NiCl(2)转换的细胞具有高端粒酶活性。在NiSO(4)转化的细胞中发现弱端粒酶。结果似乎表明,除结晶性NiS外,某些水溶性镍化合物(如NiCl(2))也具有高度致癌性。这些结果可能部分解释了不溶性结晶NiS,可溶性NiCl(2)和NiSO(4)的细胞转化和相对致癌性。版权所有2001 Wiley-Liss,Inc.

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