Roberts D, Peck C, Hilliard S, Wingo W
Cancer Res. 1979 Oct;39(10):4048-54.
Treatment with methotrexate (MTX) plus 1-beta-D-arabinofuranosylcytosine (ara-C) on Days 1, 4, and 7 after i.p. inoculation of L1210 ascites cells was more effective than treatment with one drug on Days 1, 4, and 7 followed by the second drug on Days 2, 5, and 8. Simultaneous treatment with both drugs was associated with a retention of 1-beta-D-arabinofuranosylcytosine 5'-triphosphate (ara-CTP) but no increase in the activity of deoxycytidine kinase in L1210 cells, whereas pretreatment with MTX 24 hr before the administration of ara-C was associated with approximately 2-fold increases in the level of ara-CTP and of deoxycytidine kinase in L1210 cells. However, from 5 hr after treatment with ara-C, higher levels of ara-CTP were observed in L1210 cells treated simultaneously with both drugs than in cells from animals pretreated with MTX 24 hr before treatment with ara-C. The superiority of simultaneous treatment over sequential treatment and the synergism between MTX and ara-C, previously reported for this schedule of simultaneous treatment, are attributed in part to the MTX-induced retention of ara-CTP and the increased exposure of L1210 cells to ara-CTP that results from the slower clearance of ara-CTP.
在腹腔接种L1210腹水细胞后的第1、4和7天,用甲氨蝶呤(MTX)加1-β-D-阿拉伯呋喃糖基胞嘧啶(ara-C)进行治疗比在第1、4和7天用一种药物治疗,然后在第2、5和8天用第二种药物治疗更有效。两种药物同时治疗与L1210细胞中1-β-D-阿拉伯呋喃糖基胞嘧啶5'-三磷酸(ara-CTP)的保留有关,但脱氧胞苷激酶的活性没有增加,而在给予ara-C前24小时用MTX预处理与L1210细胞中ara-CTP水平和脱氧胞苷激酶水平增加约2倍有关。然而,从用ara-C治疗后5小时起,在两种药物同时治疗的L1210细胞中观察到的ara-CTP水平高于在用ara-C治疗前24小时用MTX预处理的动物的细胞中的水平。先前报道的这种同时治疗方案中,同时治疗优于序贯治疗以及MTX与ara-C之间的协同作用,部分归因于MTX诱导的ara-CTP保留以及由于ara-CTP清除较慢导致L1210细胞对ara-CTP的暴露增加。