Suppr超能文献

对阿霉素的耐药性:阿霉素敏感和耐药的P388白血病克隆细胞系中细胞毒性与药物摄取及DNA单链和双链断裂的关系。

Resistance to adriamycin: relationship of cytotoxicity to drug uptake and DNA single- and double-strand breakage in cloned cell lines of adriamycin-sensitive and -resistant P388 leukemia.

作者信息

Goldenberg G J, Wang H, Blair G W

出版信息

Cancer Res. 1986 Jun;46(6):2978-83.

PMID:3698020
Abstract

Cloned lines of Adriamycin (ADR)-sensitive and -resistant P388 leukemia have been established from single cell cultures. A marker chromosome M1 was found in all cells in the heterogeneous resistant P388/ADR parental line as well as in the cloned resistant lines P388/ADR/3 and P388/ADR/7; a different marker chromosome M2 was present in the heterogeneous sensitive P388 parental line as well as the cloned sensitive line P388/4. Dose-survival studies showed that D0, the dose of Adriamycin reducing survival to 1/e (i.e., 37% of the initial population), was 33 +/- 5 (SE) nM for sensitive P388/4 cells, 169 +/- 17 nM for resistant P388/ADR/3 cells, and 336 +/- 28 nM for the more resistant P388/ADR/7 cells. Drug uptake in sensitive P388/4 cells was 1.6-fold greater than in resistant P388/ADR/3 cells and 2.1-fold greater than in resistant P388/ADR/7 cells. The number of DNA single-strand breaks produced per microM Adriamycin was 131 +/- 9 rad equivalents in sensitive clone 4 cells, 41 +/- 8 rad equivalents in resistant clone 3 cells, and 33 +/- 11 rad equivalents in resistant clone 7 cells. The number of DNA double-strand breaks per microM Adriamycin was 1721 +/- 126 rad equivalents in sensitive cells, 117 +/- 36 rad equivalents in resistant P388/ADR/3 cells, and 194 +/- 16 rad equivalents in resistant P388/ADR/7 cells. Differences in drug uptake were insufficient to explain the higher incidence of DNA single- and double-strand breaks in sensitive cells. These findings strongly support the concept that resistance to Adriamycin in P388 leukemia cells is multifactorial; however, this study did not resolve whether these changes arise from a single pleiotropic mutation or from multiple mutations. In sensitive P388/4 cells the number of DNA single-strand breaks formed could all be attributed to double-strand breaks. However, in both resistant cell lines the level of induction of single-strand breaks was in excess of that due to double-strand breaks, and this excess of single-strand breaks appeared to vary directly with the degree of resistance, being greater in the more resistant clone 7 cells than in the less resistant clone 3 cells. In both sensitive and resistant cell lines the ratio of true single- to double-strand breaks varied inversely with the concentration of Adriamycin. Finally, the cytotoxic activity of Adriamycin appeared to correlate more closely with formation of DNA double-strand breaks than with single-strand lesions.

摘要

已从单细胞培养物中建立了对阿霉素(ADR)敏感和耐药的P388白血病克隆系。在异质性耐药P388/ADR亲本系以及克隆的耐药系P388/ADR/3和P388/ADR/7的所有细胞中均发现了一条标记染色体M1;在异质性敏感P388亲本系以及克隆的敏感系P388/4中存在另一条不同的标记染色体M2。剂量-存活研究表明,对于敏感的P388/4细胞,将存活率降低至1/e(即初始群体的37%)的阿霉素剂量D0为33±5(SE)nM,对于耐药的P388/ADR/3细胞为169±17 nM,对于耐药性更强的P388/ADR/7细胞为336±28 nM。敏感的P388/4细胞中的药物摄取比耐药的P388/ADR/3细胞高1.6倍,比耐药的P388/ADR/7细胞高2.1倍。每微摩尔阿霉素产生的DNA单链断裂数在敏感克隆4细胞中为131±9拉德当量,在耐药克隆3细胞中为41±8拉德当量,在耐药克隆7细胞中为33±11拉德当量。每微摩尔阿霉素产生的DNA双链断裂数在敏感细胞中为1721±126拉德当量,在耐药的P388/ADR/3细胞中为117±36拉德当量,在耐药的P388/ADR/7细胞中为194±16拉德当量。药物摄取的差异不足以解释敏感细胞中DNA单链和双链断裂发生率较高的现象。这些发现有力地支持了P388白血病细胞对阿霉素的耐药性是多因素的这一概念;然而,这项研究并未解决这些变化是由单个多效性突变还是多个突变引起的。在敏感的P388/4细胞中形成的DNA单链断裂数均可归因于双链断裂。然而,在两个耐药细胞系中,单链断裂的诱导水平均超过了双链断裂所致的水平,并且这种单链断裂的过量似乎与耐药程度直接相关,在耐药性更强的克隆7细胞中比在耐药性较弱的克隆3细胞中更大。在敏感和耐药细胞系中,真正的单链与双链断裂的比例均与阿霉素浓度呈反比。最后,阿霉素的细胞毒性活性似乎与DNA双链断裂的形成比与单链损伤的相关性更密切。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验