Hilton J, Bowie D L, Gutin P H, Zito D M, Walker M D
Cancer Res. 1977 Jul;37(7 Pt 1):2262-6.
The DNA of L1210 cells exposed to low concentrations of 1-(2-chloroethyl)=3-cyclohexyl-1-nitrosourea has been analyzed for the presence of single-strand breaks. DNA from 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea-treated cells both sediments more slowly than control DNA on alkaline sucrose gradients andshows a greater extent of strand separation of the DNA helix in alkali. These effects are a typical result of exposure of cellular DNA to alkylating agents or ionizing radiation. The extent of DNA damage caused by 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea has been related to the same amount of damage resulting from exposure of cells to low doses of gamma-irradiation. The rate and extent of repair of 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea-induced damage is slow and incomplete, compared with the repair of gamma-irradiation damage to DNA. It is concluded that 1-(2-chloroethyl)-3-cyclohexyl-1-nitrosourea behaves as a weak alkylating agent, a property that may explain its antitumor properties.
已对暴露于低浓度1-(2-氯乙基)-3-环己基-1-亚硝基脲的L1210细胞的DNA进行分析,以检测单链断裂的存在情况。来自1-(2-氯乙基)-3-环己基-1-亚硝基脲处理细胞的DNA在碱性蔗糖梯度上的沉降速度比对照DNA慢,并且在碱中DNA螺旋的链分离程度更大。这些效应是细胞DNA暴露于烷化剂或电离辐射的典型结果。1-(2-氯乙基)-3-环己基-1-亚硝基脲引起的DNA损伤程度与细胞暴露于低剂量γ辐射所导致的相同程度的损伤有关。与DNA的γ辐射损伤修复相比,1-(2-氯乙基)-3-环己基-1-亚硝基脲诱导损伤的修复速率和程度缓慢且不完全。得出的结论是,1-(2-氯乙基)-3-环己基-1-亚硝基脲表现为一种弱烷化剂,这一特性可能解释了它的抗肿瘤特性。