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DNA嵌入剂3-硝基苯并噻唑并(3,2-a)喹啉鎓与DNA拓扑异构酶的相互作用:其生物活性的一种可能机制。

Interaction of DNA intercalator 3-nitrobenzothiazolo (3,2-a)quinolinium with DNA topoisomerases: a possible-mechanism for its biological activity.

作者信息

Báez A, Riou J F, Le Pecq J B, Riou G

机构信息

Laboratoire de Pharmacologie Moléculaire, Institut Gustave Roussy, Villejuif, France.

出版信息

Mol Pharmacol. 1990 Mar;37(3):377-82.

PMID:2156151
Abstract

There is multiple evidence linking the inhibition of DNA topoisomerases I and II with the cytotoxic effects of antitumor drugs such as camptothecin and the DNA intercalators, 4-(9-acridinylamino)methanesulfon-m-anisidine) (mAMSA) and Adriamycin. We have assessed the effect of the DNA intercalator 3-nitrobenzothiazolo(3,2-a)quinolinium (NBQ) on the DNA topoisomerase I and II activities. NBQ has no effect on the activity of purified topoisomerase I, whereas it induced purified topoisomerase II binding to DNA without inducing DNA scission. Above 30 microM, NBQ stimulated formation of double- and single-strand breaks mediated by topoisomerase II in plasmid DNA. Using the alkaline elution technique we determined that NBQ induced single-strand and DNA-protein-associated breaks in the human promyelocytic leukemia cell line HL-60. At sublethal concentrations (less than or equal to 1 microM), NBQ induce HL-60 cells to differentiate. Topoisomerase II-mediated DNA cleavage induced by mAMSA was substantially reduced in NBQ-differentiated cells. Our data suggest that topoisomerase II could play a major role in the biological activity of NBQ in vivo.

摘要

有多项证据表明,DNA拓扑异构酶I和II的抑制作用与喜树碱等抗肿瘤药物以及DNA嵌入剂4-(9-吖啶基氨基)甲磺酰基间甲氧基苯胺(mAMSA)和阿霉素的细胞毒性作用有关。我们评估了DNA嵌入剂3-硝基苯并噻唑并(3,2-a)喹啉鎓(NBQ)对DNA拓扑异构酶I和II活性的影响。NBQ对纯化的拓扑异构酶I的活性没有影响,而它能诱导纯化的拓扑异构酶II与DNA结合但不诱导DNA断裂。浓度高于30微摩尔时,NBQ刺激拓扑异构酶II介导的质粒DNA双链和单链断裂的形成。使用碱性洗脱技术,我们确定NBQ在人早幼粒细胞白血病细胞系HL-60中诱导单链和DNA-蛋白质相关的断裂。在亚致死浓度(小于或等于1微摩尔)下,NBQ诱导HL-60细胞分化。在NBQ分化的细胞中,mAMSA诱导的拓扑异构酶II介导的DNA切割显著减少。我们的数据表明,拓扑异构酶II可能在NBQ体内的生物学活性中起主要作用。

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