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DNA as a possible target for antitumor ruthenium(111) complexes - A spectroscopic and molecular biology study of the interactions of two representative antineoplastic ruthenium(111) complexes with DNA

机译:DNA可能成为抗肿瘤钌(111)配合物的靶标-两个代表性抗肿瘤钌(111)配合物与DNA相互作用的光谱和分子生物学研究

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摘要

The interaction of two experimental ruthenium(III)containing antitumor complexes-Na[trans-RuCl4-(DMSO)(Im)] (NAMI) and dichloro(1,2-propylendiaminetetraacetate)ruthenium (III) (RAP)-with DNA was investigated through a number of spectroscopic and molecular biology techniques, including spectrophotometry, circular dichroism, gel shift analysis, and restriction enzyme inhibition. It was found that both complexes slightly alter DNA conformation, modify its electrophoretic mobility, and inhibit DNA recognition and cleavage by some restriction enzymes, though they were less effective than cisplatin in producing such effects. Notably, the effects produced by NAMI on DNA were much larger than those induced by RAP. Implications of these results for the mechanism of action of ruthenium(III) antitumor complexes are discussed. (C) 2000 Academic Press. [References: 28]
机译:研究了两种含钌(III)的抗肿瘤复合物-Na [反式RuCl4-(DMSO)(Im)](NAMI)和二氯(1,2-丙基二胺四乙酸)钌(III)(RAP)与DNA的相互作用。通过许多光谱学和分子生物学技术,包括分光光度法,圆二色性,凝胶位移分析和限制酶抑制。已发现这两种复合物均会轻微改变DNA构象,改变其电泳迁移率,并抑制DNA的识别和某些限制酶的裂解,尽管它们在产生这种作用方面不如顺铂有效。值得注意的是,NAMI对DNA的影响远大于RAP诱导的影响。讨论了这些结果对钌(III)抗肿瘤复合物作用机理的影响。 (C)2000年学术出版社。 [参考:28]

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