Suppr超能文献

柔红霉素和阿霉素在P388白血病敏感及耐药亚系中的主动外排

Active efflux of daunorubicin and adriamycin in sensitive and resistant sublines of P388 leukemia.

作者信息

Inaba M, Kobayashi H, Sakurai Y, Johnson R K

出版信息

Cancer Res. 1979 Jun;39(6 Pt 1):2200-3.

PMID:445418
Abstract

Significantly decreased uptake and retention of daunorubicin (DAU) and Adriamycin (ADR) have been reported in sublines of P388 leukemia resistant to these anthracyclines. We studied the effects of inhibitors of oxidative phosphorylation on uptake and retention of DAU and ADR in order to characterize the transport process for these anthracyclines and to clarify further the alteration in resistant cells. In glucose-free medium, uptake of DAU and ADR was accelerated by metabolic inhibitors to a greater extent in resistant cells than in sensitive cells. Under these conditions, drug uptake was similar in sensitive and resistant cells. When glucose was added to the incubation medium in the presence of 2,4-dinitrophenol, efflux of DAU from both sensitive and resistant cells was observed. Net efflux of ADR was also observed with the resistant cells, whereas glucose markedly inhibited 2,4-dinitrophenol-stimulated uptake of ADR by the sensitive cells. Furthermore, in sensitive and resistant cells preloaded with ADR and DAU, efflux of the drugs was inhibited by the addition of 2,4-dinitrophenol. These results suggest that there is an active outward transport mechanism for anthracyclines in P388 leukemia cells and that enhanced activity of this efflux process renders cells highly resistant to the cytostatic and cytotoxic effects of ADR and DAU.

摘要

据报道,在对柔红霉素(DAU)和阿霉素(ADR)耐药的P388白血病亚系中,这两种蒽环类药物的摄取和潴留显著减少。我们研究了氧化磷酸化抑制剂对DAU和ADR摄取和潴留的影响,以表征这些蒽环类药物的转运过程,并进一步阐明耐药细胞中的改变。在无葡萄糖培养基中,代谢抑制剂对耐药细胞中DAU和ADR摄取的促进作用比对敏感细胞的促进作用更大。在这些条件下,敏感细胞和耐药细胞中的药物摄取相似。当在2,4-二硝基苯酚存在的情况下向孵育培养基中添加葡萄糖时,观察到DAU从敏感细胞和耐药细胞中流出。在耐药细胞中也观察到ADR的净流出,而葡萄糖显著抑制2,4-二硝基苯酚刺激的敏感细胞对ADR的摄取。此外,在预先加载ADR和DAU的敏感细胞和耐药细胞中,添加2,4-二硝基苯酚可抑制药物的流出。这些结果表明,P388白血病细胞中存在蒽环类药物的主动外向转运机制,并且这种流出过程活性的增强使细胞对ADR和DAU的细胞生长抑制和细胞毒性作用具有高度抗性。

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