Hung D T, Deen D F, Seidenfeld J, Marton L J
Cancer Res. 1981 Jul;41(7):2783-5.
alpha-Difluoromethylornithine, a known inhibitor of polyamine biosynthesis, significantly enhanced the cytotoxic effect of 1,3-bis(2-chloroethyl)-1-nitrosourea, a cell cycle-nonspecific agent, in 9L rat brain gliosarcoma cells in vitro. Administered as a single agent, alpha-difluoromethylornithine was not cytotoxic to 9L cells and, compared to untreated control cells, caused no perturbation of cell cycle kinetics. alpha-Difluoromethylornithine-induced depletion of intracellular polyamine levels appears to have caused the observed sensitization of 9L cells to 1,3-bis(2-chloroethyl)-1-nitrosourea. Restoration of intracellular polyamine levels by the addition of exogenous putrescine to treated 9L cells reversed this phenomenon.
α-二氟甲基鸟氨酸是一种已知的多胺生物合成抑制剂,它能显著增强1,3-双(2-氯乙基)-1-亚硝基脲(一种细胞周期非特异性药物)对体外培养的9L大鼠脑胶质瘤细胞的细胞毒性作用。单独使用时,α-二氟甲基鸟氨酸对9L细胞没有细胞毒性,与未处理的对照细胞相比,也不会引起细胞周期动力学的紊乱。α-二氟甲基鸟氨酸诱导的细胞内多胺水平降低似乎导致了观察到的9L细胞对1,3-双(2-氯乙基)-1-亚硝基脲的敏感性增加。向处理过的9L细胞中添加外源性腐胺来恢复细胞内多胺水平可逆转这一现象。