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分离出两个对拓扑异构酶II抑制剂高度敏感且对过氧化物交叉耐药的中国仓鼠卵巢细胞突变体。

Isolation of two Chinese hamster ovary cell mutants hypersensitive to topoisomerase II inhibitors and cross-resistant to peroxides.

作者信息

Davies S M, Davies S L, Harris A L, Hickson I D

机构信息

Department of Clinical Oncology, University of Newcastle upon Tyne, Medical School, United Kingdom.

出版信息

Cancer Res. 1989 Aug 15;49(16):4526-30.

PMID:2545343
Abstract

We have isolated two Chinese hamster ovary cell lines, designated ADR-4 and ADR-5, which exhibit hypersensitivity to intercalating agents and epipodophyllotoxins. These drugs are thought to exert their cytotoxicity via an interaction with the enzyme topoisomerase II. However, there is no apparent change in the level or catalytic activity of topoisomerase II in the mutant cells. Drug sensitivity does not appear to be due to increased drug transport because accumulation of radiolabeled actinomycin D is similar in mutant and wild-type cells. Both mutant cell lines show enhanced resistance to hydrogen peroxide and to organic peroxides. ADR-4 cells show a degree of temperature sensitivity. ADR-5 cells show mild sensitivity to UV irradiation. Neither cell line shows significant sensitivity to mono- or bifunctional alkylating agents, ionizing radiation, or bleomycin. Cell fusion studies indicate that the phenotype of each mutant cell line is recessive and that the mutants represent two different genetic complementation groups. These studies also indicate that ADR-4 and ADR-5 Adriamycin-sensitive mutant, ADR-1. These results indicate that sensitivity to topoisomerase II inhibitors can result from abnormalities in several genes. These drug-sensitive mutants may be useful for studying the mechanisms of cell killing by topoisomerase II inhibitors, free radicals, and heat.

摘要

我们分离出了两个中国仓鼠卵巢细胞系,命名为ADR - 4和ADR - 5,它们对嵌入剂和表鬼臼毒素表现出超敏性。这些药物被认为是通过与拓扑异构酶II相互作用来发挥其细胞毒性的。然而,突变细胞中拓扑异构酶II的水平或催化活性并没有明显变化。药物敏感性似乎并非由于药物转运增加,因为突变细胞和野生型细胞中放射性标记的放线菌素D的积累情况相似。这两个突变细胞系对过氧化氢和有机过氧化物均表现出增强的抗性。ADR - 4细胞表现出一定程度的温度敏感性。ADR - 5细胞对紫外线照射表现出轻度敏感性。这两个细胞系对单功能或双功能烷化剂、电离辐射或博来霉素均未表现出明显敏感性。细胞融合研究表明,每个突变细胞系的表型都是隐性的,且这些突变体代表两个不同的遗传互补组。这些研究还表明,ADR - 4和ADR - 5阿霉素敏感突变体ADR - 1。这些结果表明,对拓扑异构酶II抑制剂的敏感性可能由多个基因的异常引起。这些药物敏感突变体可能有助于研究拓扑异构酶II抑制剂、自由基和热导致细胞死亡的机制。

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