Fietkau R, Friede H, Maurer-Schultze B
Cancer Res. 1984 Mar;44(3):1105-13.
The effect of 1-beta-D-arabinofuranosylcytosine (ara-C) on mouse L1210 ascites tumor cells was studied in vivo with cell kinetic methods. Injection of ara-C (200 mg/kg) leads to an immediate inhibition of DNA synthesis and, thus, to a block of G1 cells at the G1-S border. This dose of ara-C kills a considerable fraction (at least 54%) of the L1210 cells. A double-labeling experiment with [3H]thymidine and [14C]thymidine which permits the distinction of cells in different cycle phases shows that ara-C kills the majority of cells in S phase, while only a minor fraction of G1 cells are lethally damaged. A multicompartment model is utilized to derive from the results of the double-labeling experiment the rates of cell loss out of the different cycle phases. Eighty-seven percent of the cells that are in S phase at the time of ara-C application and 21% of the cells in G1 are killed by ara-C. The repopulation of the tumor starts from the remaining G1 cells. A mean life span of the necrotic cells of 1.9 hr is derived from the model.
采用细胞动力学方法在体内研究了1-β-D-阿拉伯呋喃糖基胞嘧啶(阿糖胞苷,ara-C)对小鼠L1210腹水瘤细胞的作用。注射阿糖胞苷(200mg/kg)可立即抑制DNA合成,从而使G1期细胞在G1-S边界处受阻。该剂量的阿糖胞苷可杀死相当一部分(至少54%)的L1210细胞。用[3H]胸腺嘧啶核苷和[14C]胸腺嘧啶核苷进行的双标记实验能够区分不同细胞周期阶段的细胞,结果表明阿糖胞苷杀死了大多数S期细胞,而只有一小部分G1期细胞受到致命损伤。利用多室模型从双标记实验结果中得出不同细胞周期阶段的细胞损失率。在应用阿糖胞苷时处于S期的细胞中有87%以及G1期细胞中有21%被阿糖胞苷杀死。肿瘤的再增殖从剩余的G1期细胞开始。从该模型得出坏死细胞的平均寿命为1.9小时。