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在体外培养的源自中国仓鼠DC3F细胞的喜树碱抗性细胞系中拓扑异构酶I的改变。

Topoisomerase I alteration in a camptothecin-resistant cell line derived from Chinese hamster DC3F cells in culture.

作者信息

Tanizawa A, Pommier Y

机构信息

Laboratory of Molecular Pharmacology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

Cancer Res. 1992 Apr 1;52(7):1848-54.

PMID:1312902
Abstract

Camptothecin-resistant DC3F Chinese hamster lung fibroblast cell lines were obtained after mutagenic treatment with ethylmethanesulfonate and subsequent exposure to 1 microM camptothecin (CPT). The most resistant cell line, which was obtained after exposure to CPT for 10 days, was designated DC3F/C-10. Comparison of 50% inhibitory concentration values after 8-h CPT treatments showed that DC3F/C-10 cells were 134-fold resistant to CPT. Resistance was associated with marked reduction of CPT-induced DNA single-strand breaks and DNA-protein cross-links. This reduction was not due to reduced amounts of immunoreactive DNA topoisomerase I protein, although nuclear extracts from DC3F/C-10 cells had less enzyme catalytic activity than those from DC3F cells. Also, fast protein liquid chromatography-purified DNA topoisomerase I from DC3F/C-10 had lower specific catalytic activity than that from DC3F cells. DNA topoisomerase I from DC3F/C-10 was resistant to inhibition of catalytic activity and induction of DNA cleavage by CPT. These results suggest that CPT resistance in DC3F/C-10 cells is due to qualitative alteration of DNA topoisomerase I.

摘要

用甲磺酸乙酯进行诱变处理,随后暴露于1微摩尔喜树碱(CPT)后,获得了耐喜树碱的DC3F中国仓鼠肺成纤维细胞系。在暴露于CPT 10天后获得的最耐药细胞系被命名为DC3F/C-10。8小时CPT处理后的50%抑制浓度值比较表明,DC3F/C-10细胞对CPT的耐药性是134倍。耐药性与CPT诱导的DNA单链断裂和DNA-蛋白质交联的显著减少有关。这种减少不是由于免疫反应性DNA拓扑异构酶I蛋白量的减少,尽管DC3F/C-10细胞的核提取物比DC3F细胞的核提取物具有更低的酶催化活性。此外,从DC3F/C-10中通过快速蛋白质液相色谱纯化的DNA拓扑异构酶I比从DC3F细胞中纯化的具有更低的比催化活性。DC3F/C-10的DNA拓扑异构酶I对CPT抑制催化活性和诱导DNA裂解具有抗性。这些结果表明,DC3F/C-10细胞中的CPT耐药性是由于DNA拓扑异构酶I的性质改变。

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