Weinkam R J, Deen D F
Cancer Res. 1982 Mar;42(3):1008-14.
A dose-response relation for the cytotoxic activity of chloroethylnitrosourea cancer chemotherapeutic agents in cell culture has been developed. Data for the activity of 1,3-bis(2-chloroethyl)-1-nitrosourea, 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea, 1-(2-chloroethyl)-3-(trans-4-methylcyclohexyl)-1-nitrosourea, and 1-(2-chloroethyl)-3-(piperidine-3,6-dion-3-yl)-1-nitrosourea against 9L rat brain tumor cells are presented. Cytotoxicity resulting from treatment schedules at different initial drug concentrations, exposure periods, and preincubation periods are correlated using a proposed dose function. Equations are presented that incorporate drug concentration, duration of exposure of cells, and the rate constant for conversion of the drug from an active intermediate into a single dose function. When compared in this way, all cell treatment schedules used were found to be equally effective in killing cells in culture. The cytotoxic activity of the four different chloroethyl-nitrosourea analogs were also found to be the same. These data demonstrate the application of quantitative dose-response relations to the activity of chloroethylnitrosoureas in cell culture and provide new insight into the mechanism of action and structure-activity relationships of these compounds.
已建立了氯乙基亚硝基脲类癌症化疗药物在细胞培养中的细胞毒性活性的剂量反应关系。给出了1,3-双(2-氯乙基)-1-亚硝基脲、1-(2-氯乙基)-3-环己基-1-亚硝基脲、1-(2-氯乙基)-3-(反式-4-甲基环己基)-1-亚硝基脲和1-(2-氯乙基)-3-(哌啶-3,6-二酮-3-基)-1-亚硝基脲对9L大鼠脑肿瘤细胞活性的数据。使用提出的剂量函数,对不同初始药物浓度、暴露时间和预温育时间的治疗方案所产生的细胞毒性进行了关联。给出了包含药物浓度、细胞暴露持续时间以及药物从活性中间体转化的速率常数的单一剂量函数的方程。以这种方式进行比较时,发现所有使用的细胞治疗方案在杀死培养细胞方面同样有效。还发现四种不同的氯乙基亚硝基脲类似物的细胞毒性活性相同。这些数据证明了定量剂量反应关系在氯乙基亚硝基脲类药物细胞培养活性中的应用,并为这些化合物的作用机制和构效关系提供了新的见解。