Yamashita Y, Kawada S, Fujii N, Nakano H
Tokyo Research Laboratories, Kyowa Hakko Kogyo Co. Ltd., Japan.
Cancer Res. 1990 Sep 15;50(18):5841-4.
Streptonigrin, a nonintercalative antitumor antibiotic, induced mammalian topoisomerase II dependent DNA cleavage in vitro. The cleavage activity of streptonigrin was comparable to that of demethylepipodophyllotoxin ethylidene-beta-D-glucoside at a low concentration (less than or equal to 10 microM) but one-third lower at a higher concentration (greater than 250 microM). Exposure of a reaction mixture containing streptonigrin, DNA, and topoisomerase II to an elevated temperature (65 degrees C) resulted in substantial reduction in DNA cleavage, suggesting that the mechanism of the topoisomerase II dependent DNA cleavage induced by streptonigrin was through the formation of a cleavage complex previously reported for topoisomerase II poisons such as 4'-(9-acridinylamino) methanesulfon-m-anisidide and epipodophyllotoxins.
链黑菌素是一种非嵌入性抗肿瘤抗生素,在体外可诱导哺乳动物拓扑异构酶II依赖性DNA裂解。在低浓度(小于或等于10微摩尔)时,链黑菌素的裂解活性与去甲基表鬼臼毒素乙叉基-β-D-葡萄糖苷相当,但在高浓度(大于250微摩尔)时则低三分之一。将含有链黑菌素、DNA和拓扑异构酶II的反应混合物加热至高温(65摄氏度)会导致DNA裂解大幅减少,这表明链黑菌素诱导的拓扑异构酶II依赖性DNA裂解机制是通过形成一种先前报道的拓扑异构酶II毒物(如4'-(9-吖啶基氨基)甲磺酰间茴香胺和表鬼臼毒素)的裂解复合物。