Tsurusawa M, Niwa M, Katano N, Fujimoto T
Department of Pediatrics, Aichi Medical University.
Jpn J Cancer Res. 1990 Jan;81(1):85-90. doi: 10.1111/j.1349-7006.1990.tb02511.x.
The association between cytotoxicity and cell cycle perturbation caused by methotrexate (MTX) was investigated in mouse L1210 leukemia cells by flow cytometric bromodeoxyuridine/DNA assay. In the range of concentrations of MTX from 10(-7) M to 10-6) M, in vitro exposure to the drug for 6 h caused a dose-dependent suppression of clonal growth of the tumor cells and S phase arrest in the cycle progression, resulting in an accumulation of cells in early S phase, in which they showed no definite increase of DNA content above G1 levels. The surviving fraction of the clonogenic cells corresponded with the fraction of cells which recovered from the S phase arrest in MTX-free medium. In mice bearing L1210 ascites tumors, a bolus injection of MTX caused the S phase arrest of the tumor cells as shown in suspension cultures, and cytokinetic recovery was observed in parallel with the regrowth of the tumor. These results showed that irreversible S phase arrest is a critical cytokinetic event associated with the cytotoxicity of MTX.
通过流式细胞术溴脱氧尿苷/DNA检测法,在小鼠L1210白血病细胞中研究了甲氨蝶呤(MTX)引起的细胞毒性与细胞周期扰动之间的关联。在MTX浓度范围为10^(-7) M至10^(-6) M时,体外将细胞暴露于该药物6小时会导致肿瘤细胞克隆生长受到剂量依赖性抑制,并且细胞周期进程中的S期停滞,导致细胞在早期S期积累,在此阶段细胞DNA含量未显示出在G1水平之上有明确增加。克隆形成细胞的存活分数与在无MTX培养基中从S期停滞恢复的细胞分数相对应。在携带L1210腹水瘤的小鼠中,如悬浮培养所示,一次大剂量注射MTX会导致肿瘤细胞的S期停滞,并且观察到细胞动力学恢复与肿瘤再生长平行。这些结果表明,不可逆的S期停滞是与MTX细胞毒性相关的关键细胞动力学事件。