Santelli G, Valeriote F
J Natl Cancer Inst. 1978 Sep;61(3):843-7.
The spleen colony assay was used to examine the effect of thymidine (dThd) on 5-fluorouracil (FUra) cytotoxicity in two transplantable leukemias, AKR (in AKR mice) and L1210 [in (BALB/c x DBA/2)F1 mice], in vivo. A large dose of dThd (10 mg/mouse) could not rescue these cell lines from FUra toxicity. Instead, when dThd was given within 1 hour before FUra, it enhanced FUra cytotoxicity by a factor between 100 and 1,000 in AKR leukemia. That dThd increased the cytotoxicity of FUra only by a factor of 3 in L1210 leukemia suggested a different mechanism of interaction of the two drugs in the two cell lines. Examination in hybrid mice capable of supporting the growth of both leukemias showed the enhancement to be tumor related rather than host related. We also demonstrated a dose-dependent effect of dThd injection 15 minutes before FUra in AKR leukemia. Concerning the kinetics of killing of AKR leukemia colony-forming units (LCFU) following the administration of dThd 15 minutes before FUra, LCFU survival continued to decrease for 24--36 hours following drug administration.
采用脾集落试验在体内研究胸苷(dThd)对两种可移植白血病(AKR白血病,AKR小鼠模型;L1210白血病,(BALB/c×DBA/2)F1小鼠模型)中5-氟尿嘧啶(FUra)细胞毒性的影响。大剂量的dThd(10mg/小鼠)无法使这些细胞系免受FUra的毒性作用。相反,当在FUra给药前1小时内给予dThd时,它会使AKR白血病中FUra的细胞毒性增强100至1000倍。而在L1210白血病中,dThd仅使FUra的细胞毒性增加3倍,这表明两种药物在这两种细胞系中的相互作用机制不同。对能够支持两种白血病生长的杂交小鼠进行研究表明,这种增强作用与肿瘤相关而非与宿主相关。我们还证明了在AKR白血病中,在FUra给药前15分钟注射dThd存在剂量依赖性效应。关于在FUra给药前15分钟给予dThd后AKR白血病集落形成单位(LCFU)的杀伤动力学,给药后LCFU的存活率在24 - 36小时内持续下降。