DNA topoisomerase II mutations and resistance to anti‐tumor drugs

DNA topoisomerase II mutations and resistance to anti‐tumor drugs
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DNA拓扑异构酶II突变与抗肿瘤药物耐药

DOI:
10.1002/bies.950170906
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发表时间:
1995
期刊:
影响因子:
4
通讯作者:
S. Gasser
S. Gasser
中科院分区:
生物学3区
文献类型:
--
作者:
Y. Vassetzky;G. Alghisi;S. Gasser

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DNA拓扑异构酶II的突变通常与肿瘤细胞系的耐药性有关。各种模型系统中拓扑异构酶II介导的耐药研究,以及耐药肿瘤中这些突变的测序,揭示了拓扑异构酶II的功能域,它如何与抑制剂相互作用,以及细胞避免许多临床重要抗肿瘤药物毒性作用的不同机制。
Mutations in DNA topoisomerase II are often correlated with drug‐resistance in tumor cell lines. Studies of topoisomerase II‐mediated drug‐resistance in various model systems, as well as the sequencing of such mutations from drug‐resistant tumors, have shed light on the functional domains of topoisomerase II, on how it interacts with inhibitors, and on the different mechanisms by which cells avoid the toxic effects of many clinically important anti‐tumor drugs.
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