Suppr超能文献

人癌KB细胞依托泊苷耐药突变体中DNA拓扑异构酶II磷酸化增加。

Increased phosphorylation of DNA topoisomerase II in etoposide-resistant mutants of human cancer KB cells.

作者信息

Takano H, Kohno K, Ono M, Uchida Y, Kuwano M

机构信息

Department of Biochemistry, Oita Medical School, Japan.

出版信息

Cancer Res. 1991 Aug 1;51(15):3951-7.

PMID:1649696
Abstract

We have isolated two etoposide (VP16)-resistant cell lines, KB/VP-1 and KB/VP-2, from human cancer KB cells after stepwise exposure to increasing doses of VP16. KB/VP-1 and KB/VP-2 showed 30- and 50-fold higher resistance to VP16 and also 20- and 30-fold higher resistance to teniposide than the parent cell line. Furthermore, both resistant cell lines showed more than 2-fold cross-resistance to Adriamycin and daunomycin than KB cells. The levels of accumulation and outward transport of radioactive VP16 were similar in KB/VP-1, KB/VP-2, and KB. The activity of nuclear extracts of DNA topoisomerase II for both KB/VP-1 and KB/VP-2 assayed by decatenation of kinetoplast DNA was consistently similar to that of KB. However, in both immunoblot assay with specific anti-topoisomerase II antibody and Northern blot analysis with specific human DNA topoisomerase II complementary DNA, cellular levels of topoisomerase II in both resistant cell lines were less than one-tenth the level in KB. The cellular levels of DNA topoisomerase I, however, were similar between the mutants and their parent. A quantitative precipitation assay of covalent DNA-topoisomerase II complexes showed greatly reduced VP16-induced cleavages of 3'-32P-DNA by nuclear extracts of KB/VP-1 or KB/VP-2 cells in comparison with KB cells. The relative specific phosphorylation of DNA topoisomerase II was about 14- to 18-fold higher in the mutants than in the parental cells. Phosphoamino acid analysis of DNA topoisomerase II showed that serine was the phosphorylated amino acid in all three cell lines, KB, KB/VP-1, and KB/VP-2. These data suggest that reduced expression of DNA-topoisomerase II might account for the acquired VP16 resistance and reduced VP16-induced cleavages of DNA-topoisomerase II complexes in both VP16-resistant variants.

摘要

我们通过逐步增加依托泊苷(VP16)的剂量,从人癌KB细胞中分离出了两株对VP16耐药的细胞系,即KB/VP-1和KB/VP-2。与亲代细胞系相比,KB/VP-1和KB/VP-2对VP16的耐药性高30倍和50倍,对替尼泊苷的耐药性高20倍和30倍。此外,这两株耐药细胞系对阿霉素和柔红霉素的交叉耐药性比KB细胞高2倍以上。放射性VP16在KB/VP-1、KB/VP-2和KB中的积累水平和外向转运水平相似。通过动质体DNA解连环测定的KB/VP-1和KB/VP-2的DNA拓扑异构酶II核提取物活性与KB的活性始终相似。然而,在使用特异性抗拓扑异构酶II抗体的免疫印迹分析和使用特异性人DNA拓扑异构酶II互补DNA的Northern印迹分析中,这两株耐药细胞系中的拓扑异构酶II细胞水平均不到KB中水平的十分之一。然而,DNA拓扑异构酶I的细胞水平在突变体及其亲代之间相似。共价DNA-拓扑异构酶II复合物的定量沉淀分析表明,与KB细胞相比,KB/VP-1或KB/VP-2细胞的核提取物对VP16诱导的3'-32P-DNA切割大大减少。DNA拓扑异构酶II的相对特异性磷酸化在突变体中比亲代细胞高约14至18倍。DNA拓扑异构酶II的磷酸氨基酸分析表明,丝氨酸是KB、KB/VP-1和KB/VP-2这三株细胞系中被磷酸化的氨基酸。这些数据表明,DNA拓扑异构酶II表达降低可能是这两株VP16耐药变体获得性VP16耐药性以及VP16诱导的DNA拓扑异构酶II复合物切割减少的原因。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验