Matsumura S, Hoshino T, Weizsaecker M, Deen D F
Cancer Treat Rep. 1983 May;67(5):475-80.
9L rat brain tumor cells were continuously exposed to "low" (2.9 microM) and "high" (18 and 35 microM) doses of 6-mercaptopurine (6-MP); cell kill was measured with a colony forming efficiency assay. The low dose of 6-MP killed more cells than the high doses, as measured by surviving fraction, when they were treated for greater than 48 hours. Even though the total number of cells increased during the 72-hour treatment period, the number of clonogenic cells decreased most when cells were treated with the low dose of 6-MP. Data obtained with flow cytometry suggest that for the high dose there was a drug-induced block of cells in the G1 phase that prevented them from progression into S phase where they would be killed.
将9L大鼠脑肿瘤细胞持续暴露于“低”(2.9微摩尔)和“高”(18和35微摩尔)剂量的6-巯基嘌呤(6-MP);通过集落形成效率测定法测量细胞杀伤情况。当处理时间超过48小时时,以存活分数衡量,低剂量的6-MP比高剂量杀死的细胞更多。尽管在72小时的处理期间细胞总数增加,但用低剂量6-MP处理时,克隆形成细胞的数量减少最多。流式细胞术获得的数据表明,对于高剂量,药物诱导细胞在G1期阻滞,阻止它们进入会被杀死的S期。