Ross W E, Ewig R A, Kohn K W
Cancer Res. 1978 Jun;38(6):1502-6.
The formation of DNA cross-links is thought to represent the lethal lesion following exposure of cells to bifunctional alkylating agents. Since differences in rates of formation and repair of cross-links may explain differences in activity of these agents, we have studied these events following exposure of L1210 cells to nitrogen mustard (HN2) and melphalan. With the technique of alkaline elution, it was possible to measure cross-linking at doses that result in relatively little cell kill. Following a 30-min exposure to HN2, DNA cross-links increased for 1 to 2 hr and were then removed by a process that was virtually complete in 24 hr. In contrast, following a 30-min exposure to melphalan, cross-link formation increased for 12 hr and removal was much slower than it was for HN2. Comparison of cell survival with cross-linking kinetics suggests that persistence of the cross-links with time is an important factor in determining lethality.
DNA交联的形成被认为是细胞暴露于双功能烷化剂后产生的致死性损伤。由于交联形成和修复速率的差异可能解释这些药物活性的差异,我们研究了L1210细胞暴露于氮芥(HN2)和美法仑后这些事件的发生情况。采用碱性洗脱技术,可以在导致相对较少细胞死亡的剂量下测量交联情况。在暴露于HN2 30分钟后,DNA交联增加1至2小时,然后通过一个在24小时内基本完成的过程被去除。相比之下,在暴露于美法仑30分钟后,交联形成增加12小时,且去除速度比HN2慢得多。将细胞存活率与交联动力学进行比较表明,交联随时间的持续存在是决定致死率的一个重要因素。