Kondo Natsuko, Takahashi Akihisa, Ono Koji, Ohnishi Takeo
Particle Radiation Oncology Research Center, Research Reactor Institute, Kyoto University, Kumatori-cho, Sennan-gun, Osaka 590-0494, Japan.
J Nucleic Acids. 2010 Nov 21;2010:543531. doi: 10.4061/2010/543531.
The cytotoxic effects of alkylating agents are strongly attenuated by cellular DNA repair processes, necessitating a clear understanding of the repair mechanisms. Simple methylating agents form adducts at N- and O-atoms. N-methylations are removed by base excision repair, AlkB homologues, or nucleotide excision repair (NER). O(6)-methylguanine (MeG), which can eventually become cytotoxic and mutagenic, is repaired by O(6)-methylguanine-DNA methyltransferase, and O(6)MeG:T mispairs are recognized by the mismatch repair system (MMR). MMR cannot repair the O(6)MeG/T mispairs, which eventually lead to double-strand breaks. Bifunctional alkylating agents form interstrand cross-links (ICLs) which are more complex and highly cytotoxic. ICLs are repaired by complex of NER factors (e.g., endnuclease xeroderma pigmentosum complementation group F-excision repair cross-complementing rodent repair deficiency complementation group 1), Fanconi anemia repair, and homologous recombination. A detailed understanding of how cells cope with DNA damage caused by alkylating agents is therefore potentially useful in clinical medicine.
细胞DNA修复过程会显著减弱烷化剂的细胞毒性作用,因此有必要清楚了解其修复机制。简单的甲基化剂会在氮原子和氧原子处形成加合物。N-甲基化可通过碱基切除修复、AlkB同源物或核苷酸切除修复(NER)去除。O(6)-甲基鸟嘌呤(MeG)最终可能具有细胞毒性和致突变性,可由O(6)-甲基鸟嘌呤-DNA甲基转移酶修复,而O(6)MeG:T错配可由错配修复系统(MMR)识别。MMR无法修复O(6)MeG/T错配,最终导致双链断裂。双功能烷化剂会形成链间交联(ICL),这种交联更为复杂且具有高度细胞毒性。ICL由NER因子复合物(如着色性干皮病互补组F-切除修复交叉互补啮齿动物修复缺陷互补组1内切酶)、范可尼贫血修复和同源重组进行修复。因此,详细了解细胞如何应对烷化剂引起的DNA损伤在临床医学中可能具有重要意义。