Gorbacheva L B, Kukushkina G V, Elksne S J, Miniker T D, Preobrazhenskaya M N
Institute of Chemical Physics, Academy of Sciences of the USSR, Moscow.
Anticancer Drugs. 1991 Apr;2(2):185-9. doi: 10.1097/00001813-199104000-00009.
The effect of O6-methylguanine (O6-MeG) on the therapeutic efficiency of 1-methyl-1-nitrosourea (MNU) and 1,3-bis-(2-chloroethyl)-1-nitrosourea (BCNU) against the murine L1210 leukemia and B16 melanoma was studied in vivo. Although the level of O6-alkylguanine-DNA alkyltransferase (AGT) in L1210/BCNU leukemia cells was three times higher than in L1210 leukemia cells, no enhancement of the antitumor activity of MNU and BCNU in L1210 leukemia or B16 melanoma with O6-MeG or MNU potentiated markedly the cytotoxic effects of MNU and BCNU. Administration of O6-MeG to mice bearing L1210 leukemia led to delayed inhibition of DNA synthesis and appearance of long-term single-strand breaks in DNA of tumor cells.
在体内研究了O6-甲基鸟嘌呤(O6-MeG)对1-甲基-1-亚硝基脲(MNU)和1,3-双(2-氯乙基)-1-亚硝基脲(BCNU)治疗小鼠L1210白血病和B16黑色素瘤疗效的影响。尽管L1210/BCNU白血病细胞中O6-烷基鸟嘌呤-DNA烷基转移酶(AGT)的水平比L1210白血病细胞高三倍,但在L1210白血病或B16黑色素瘤中,O6-MeG或MNU并未增强MNU和BCNU的抗肿瘤活性,而MNU显著增强了MNU和BCNU的细胞毒性作用。给患有L1210白血病的小鼠施用O6-MeG会导致DNA合成的延迟抑制以及肿瘤细胞DNA中出现长期的单链断裂。