首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Ethidium bromide changes the nuclease-sensitive DNA binding sites of the antitumor drug cis-diamminedichloroplatinum(II).
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Ethidium bromide changes the nuclease-sensitive DNA binding sites of the antitumor drug cis-diamminedichloroplatinum(II).

机译:溴乙锭改变了抗肿瘤药物顺二氨二氯铂(II)的核酸酶敏感DNA结合位点。

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摘要

Exonuclease III has been shown previously to reveal the binding sites of the antitumor drug cis-diamminedichloroplatinum(II) on DNA. Pretreatment of the same DNA with the intercalator ethidium bromide causes new platinum binding sites to be detected by the exonuclease III method. In particular, a 5'd(G6-D-G2)3' sequence in a 165-base-pair restriction fragment of plasmid pBR322 becomes a preferred site for exonuclease III-detectable cis-diamminedichloroplatinum(II)binding. This switching of nuclease-sensitive platinum binding to new sites by the influence of another drug, ethidium bromide, offers an explantation at the molecular level for the phenomenon of synergism in combination chemotherapy.
机译:核酸外切酶III先前已显示出抗肿瘤药物顺二氨二氯铂(II)在DNA上的结合位点。用嵌入剂溴化乙锭预处理相同的DNA可以通过核酸外切酶III方法检测到新的铂结合位点。特别地,质粒pBR322的165个碱基对的限制性片段中的5'd(G6-D-G2)3'序列成为核酸外切酶III可检测的顺式-二氨基二氯铂(II)结合的优选位点。在另一种药物溴化乙锭的影响下,核酸酶敏感的铂结合到新位点的这种转换为联合化疗中的协同现象提供了分子水平的外植。

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