O6-alkylguanine-DNA alkyltransferase:: role in carcinogenesis and chemotherapy

被引:177
作者
Margison, GP [1 ]
Santibáñez-Koref, MF
机构
[1] Paterson Inst Canc Res, CRC Carcinogenesis Grp, Manchester M20 9BX, Lancs, England
[2] Max Delbruck Ctr Mol Med, Berlin, Germany
关键词
D O I
10.1002/bies.10063
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The DNA in human cells is continuously undergoing damage as consequences of both endogenous processes and exposure to exogenous agents. The resulting structural changes can be repaired by a number of systems that function to preserve genome integrity. Most pathways are multicomponent, involving incision in the damaged DNA strand and resynthesis using the undamaged strand as a template. In contrast, O-6-alkylguanine-DNA alkyltransferase is able to act as a single protein that reverses specific types of alkylation damage simply by removing the offending alkyl group, which becomes covalently attached to the protein and inactivates it. The types of damage that ATase repairs are potentially toxic, mutagenic, recombinogenic and clastogenic. They are generated by certain classes of carcinogenic and chemotherapeutic alkylating agents. There is consequently a great deal of interest in this repair system in relation to both carcinogenesis and cancer chemotherapy. BioEssays 24:255-266,2002. (C) 2002 Wiley Periodicals, Inc.;
引用
收藏
页码:255 / 266
页数:12
相关论文
共 83 条
[1]   Bacterial and mammalian DNA alkyltransferases sensitize Escherichia coli to the lethal and mutagenic effects of dibromoalkanes [J].
Abril, N ;
LuqueRomero, FL ;
PrietoAlamo, MJ ;
Rafferty, JA ;
Margison, GP ;
Pueyo, C .
CARCINOGENESIS, 1997, 18 (10) :1883-1888
[2]   Implication of localization of human DNA repair enzyme O6-methylguanine-DNA methyltransferase at active transcription sites in transcription-repair coupling of the mutagenic O6-methylguanine lesion [J].
Ali, RB ;
Teo, AKC ;
Oh, HK ;
Chuang, LSH ;
Ayi, TC ;
Li, BFL .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (03) :1660-1669
[3]  
Aquilina G, 1998, CANCER RES, V58, P135
[4]   NON-ENZYMATIC METHYLATION OF DNA BY S-ADENOSYLMETHIONINE INVITRO [J].
BARROWS, LR ;
MAGEE, PN .
CARCINOGENESIS, 1982, 3 (03) :349-351
[5]  
Bearzatto A, 2000, CANCER RES, V60, P3262
[6]   INTERFERON INDUCERS INCREASE O-6-ALKYLGUANINE-DNA ALKYLTRANSFERASE IN THE RAT-LIVER [J].
BERTINI, R ;
COCCIA, P ;
PAGANI, P ;
MARINELLO, C ;
SALMONA, M ;
DINCALCI, M .
CARCINOGENESIS, 1990, 11 (01) :181-183
[7]   Regulation of the human O6-methylguanine-DNA methyltransferase gene by transcriptional coactivators cAMP response element-binding protein-binding protein and p300 [J].
Bhakat, KK ;
Mitra, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (44) :34197-34204
[8]   O-6-METHYLGUANINE-DNA METHYLTRANSFERASE ACTIVITY AND INDUCTION OF NOVEL IMMUNOGENICITY IN MURINE TUMOR-CELLS TREATED WITH METHYLATING AGENTS [J].
BIANCHI, R ;
CITTI, L ;
BEGHETTI, R ;
ROMANI, L ;
DINCALCI, M ;
PUCCETTI, P ;
FIORETTI, MC .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1992, 29 (04) :277-282
[9]   Unmasking a killer:: DNA O6-methylguanine and the cytotoxicity of methylating agents [J].
Bignami, M ;
O'Driscoll, M ;
Aquilina, G ;
Karran, P .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2000, 462 (2-3) :71-82
[10]   Activation of human O6-methylguanine-DNA methyltransferase gene by glucocorticoid hormone [J].
Biswas, T ;
Ramana, CV ;
Srinivasan, G ;
Boldogh, I ;
Hazra, TK ;
Chen, ZP ;
Tano, K ;
Thompson, EB ;
Mitra, S .
ONCOGENE, 1999, 18 (02) :525-532