Marton L J, Levin V A, Hervatin S J, Koch-Weser J, McCann P P, Sjoerdsma A
Cancer Res. 1981 Nov;41(11 Pt 1):4426-31.
alpha-Difluoromethylornithine (DFMO), an enzyme-activated irreversible inhibitor of ornithine decarboxylase, was used alone and in combination with various single doses of 1,3-bis(2-chloroethyl)-1-nitrosourea (BCNU) to treat animals bearing murine glioma 26 and rat 9L gliosarcoma intracerebral tumors. Used as a single agent, DFMO has little or no effect against these tumors. However, in both intracerebral tumor models, pretreatment with DFMO p.o. before i.p. administration of BCNU potentiates the effect of BCNU without increasing toxicity. The effects of DFMO administered p.o. after BCNU or before and after various doses of BCNU indicate that DFMO may also effectively slow the repopulation of these tumors after BCNU therapy.
α-二氟甲基鸟氨酸(DFMO)是一种鸟氨酸脱羧酶的酶激活不可逆抑制剂,单独使用以及与各种单剂量的1,3-双(2-氯乙基)-1-亚硝基脲(BCNU)联合使用,用于治疗患有鼠胶质瘤26和大鼠9L脑内胶质瘤的动物。作为单一药物使用时,DFMO对这些肿瘤几乎没有影响。然而,在两种脑内肿瘤模型中,在腹腔注射BCNU之前口服DFMO进行预处理,可增强BCNU的效果而不增加毒性。在BCNU之后口服DFMO或在不同剂量的BCNU之前和之后口服DFMO的效果表明,DFMO还可能有效地减缓BCNU治疗后这些肿瘤的再增殖。