Oredsson S M, Gray J W, Deen D F, Marton L J
Cancer Res. 1983 Jun;43(6):2541-4.
The effect of pretreating 9L rat brain tumor cells in vitro with 10 mM alpha-difluoromethylornithine (DFMO), an enzyme-activated, irreversible inhibitor of ornithine decarboxylase, on the cytotoxicity of 1-beta-D-arabinofuranosylcytosine (ara-C) was investigated using a colony-forming assay. DFMO-mediated polyamine depletion significantly decreased the cytotoxicity of ara-C. The addition of putrescine to DFMO-pretreated cells replenishes intracellular polyamine levels and prevents the decrease in ara-C cytotoxicity. Flow cytometric analysis showed that cells treated with ara-C alone entered S phase semisynchronously within 8 hr after the end of treatment. This phenomenon was virtually eliminated by DFMO pretreatment. Addition of putrescine to DFMO-pretreated cells before treatment with ara-C prevented this DFMO-induced cell cycle kinetic effect.
使用集落形成试验研究了用10 mM α-二氟甲基鸟氨酸(DFMO,一种鸟氨酸脱羧酶的酶激活不可逆抑制剂)对9L大鼠脑肿瘤细胞进行体外预处理,对1-β-D-阿拉伯呋喃糖基胞嘧啶(ara-C)细胞毒性的影响。DFMO介导的多胺耗竭显著降低了ara-C的细胞毒性。向经DFMO预处理的细胞中添加腐胺可补充细胞内多胺水平,并防止ara-C细胞毒性降低。流式细胞术分析表明,单独用ara-C处理的细胞在处理结束后8小时内半同步进入S期。DFMO预处理几乎消除了这种现象。在用ara-C处理之前,向经DFMO预处理的细胞中添加腐胺可防止这种由DFMO诱导的细胞周期动力学效应。