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亚砷酸钠增强DNA交联剂的致染色体断裂性和致突变性。

Sodium arsenite potentiates the clastogenicity and mutagenicity of DNA crosslinking agents.

作者信息

Lee T C, Lee K C, Tzeng Y J, Huang R Y, Jan K Y

出版信息

Environ Mutagen. 1986;8(1):119-28. doi: 10.1002/em.2860080111.

Abstract

To see if sodium arsenite enhances the clastogenicity and the mutagenicity of DNA crosslinking agents, Chinese hamster ovary (CHO) cells and human skin fibroblasts were exposed to cis-diamminedichloroplatinum (II) (cis-Pt(II)) or 8-methoxypsoralen (8-MOP) plus long-wave ultraviolet light (UVA) and then to sodium arsenite. The results indicate that the clastogenicity of cis-Pt(II) and 8-MOP plus UVA are enhanced by the post-treatment with sodium arsenite. Chromatid breaks and exchanges are predominantly increased in doubly treated cells. Furthermore, the mutagenicity of cis-Pt(II) at the hypoxanthine-guanine phosphoribosyl transferase locus is also potentiated by sodium arsenite in CHO cells.

摘要

为了探究亚砷酸钠是否会增强DNA交联剂的致断裂性和致突变性,将中国仓鼠卵巢(CHO)细胞和人皮肤成纤维细胞暴露于顺二氯二氨铂(II)(顺铂(II))或8-甲氧基补骨脂素(8-MOP)加长波紫外线(UVA),然后再暴露于亚砷酸钠。结果表明,亚砷酸钠的后续处理增强了顺铂(II)和8-MOP加UVA的致断裂性。在双重处理的细胞中,染色单体断裂和交换主要增加。此外,亚砷酸钠还增强了顺铂(II)在CHO细胞次黄嘌呤-鸟嘌呤磷酸核糖转移酶位点的致突变性。

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