Unmasking a killer:: DNA O6-methylguanine and the cytotoxicity of methylating agents

被引:161
作者
Bignami, M
O'Driscoll, M
Aquilina, G
Karran, P
机构
[1] Imperial Canc Res Fund, Clare Hall Labs, S Mimms EN6 3LD, Herts, England
[2] Ist Super Sanita, I-00161 Rome, Italy
关键词
O-6-methylguanine; cytotoxicity; mismatch repair; mutation induction;
D O I
10.1016/S1383-5742(00)00016-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Methylating agents are potent carcinogens that are mutagenic and cytotoxic towards bacteria and mammalian cells. Their effects can be ascribed to an ability to modify DNA covalently, Pioneering studies of the chemical reactivity of methylating agents towards DNA components and their effectiveness as animal carcinogens identified O-6-methylguanine (O(6)meG) as a potentially important DNA lesion. Subsequent analysis of the effects of methylating carcinogens in bacteria and cultured mammalian cells - including the discovery of the inducible adaptive response to alkylating agents in Escherichia coli have defined the contributions of O(6)meG and other methylated DNA bases to the biological effects of these chemicals. More recently, the role of O(6)meG in killing mammalian cells has been revealed by the lethal interaction between persistent DNA O(6)meG and the mismatch repair pathway. Here, we briefly review the results which led to the identification of the biological consequences of persistent DNA O(6)meG. We consider the possible consequences for a human cell of chronic exposure to low levels of a methylating agent. Such exposure may increase the probability that the cell's mismatch repair pathway becomes inactive. Loss of mismatch repair predisposes the cell to mutation induction, not only through uncorrected replication errors but also by methylating agents and other mutagens. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:71 / 82
页数:12
相关论文
共 63 条
[11]   OVEREXPRESSION OF N-METHYLPURINE-DNA GLYCOSYLASE IN CHINESE-HAMSTER OVARY CELLS RENDERS THEM MORE SENSITIVE TO THE PRODUCTION OF CHROMOSOMAL-ABERRATIONS BY METHYLATING AGENTS - A CASE OF IMBALANCED DNA-REPAIR [J].
COQUERELLE, T ;
DOSCH, J ;
KAINA, B .
MUTATION RESEARCH-DNA REPAIR, 1995, 336 (01) :9-17
[12]   HUMAN-BRAIN TUMOR-CELL STRAINS WITH DEFICIENT HOST-CELL REACTIVATION OF N-METHYL-N'-NITRO-N-NITROSOGUANIDINE-DAMAGED ADENOVIRUS-5 [J].
DAY, RS ;
ZIOLKOWSKI, CHJ .
NATURE, 1979, 279 (5716) :797-799
[13]   DEFECTIVE REPAIR OF ALKYLATED DNA BY HUMAN-TUMOR AND SV40-TRANSFORMED HUMAN CELL STRAINS [J].
DAY, RS ;
ZIOLKOWSKI, CHJ ;
SCUDIERO, DA ;
MEYER, SA ;
LUBINIECKI, AS ;
GIRARDI, AJ ;
GALLOWAY, SM ;
BYNUM, GD .
NATURE, 1980, 288 (5792) :724-727
[14]  
de Wind N, 1998, CANCER RES, V58, P248
[15]   DEPLETION OF O-6-METHYLGUANINE-DNA-METHYLTRANSFERASE IN HUMAN-FIBROBLASTS INCREASES THE MUTAGENIC RESPONSE TO N-METHYL-N'-NITRO-N-NITROSOGUANIDINE [J].
DOMORADZKI, J ;
PEGG, AE ;
DOLAN, ME ;
MAHER, VM ;
MCCORMICK, JJ .
CARCINOGENESIS, 1985, 6 (12) :1823-1826
[16]   1,N-6-ETHENOADENINE IS PREFERRED OVER 3-METHYLADENINE AS SUBSTRATE BY A CLONED HUMAN N-METHYLPURINE DNA GLYCOSYLASE (3-METHYLADENINE DNA GLYCOSYLASE) [J].
DOSANJH, MK ;
ROY, R ;
MITRA, S ;
SINGER, B .
BIOCHEMISTRY, 1994, 33 (07) :1624-1628
[17]   Alkylpurine-DNA-N-glycosylase knockout mice show increased susceptibility to induction of mutations by methyl methanesulfonate [J].
Elder, RH ;
Jansen, JG ;
Weeks, RJ ;
Willington, MA ;
Deans, B ;
Watson, PJ ;
Mynett, KJ ;
Bailey, JA ;
Cooper, DP ;
Rafferty, JA ;
Heeran, MC ;
Wijnhoven, SWP ;
van Zeeland, AA ;
Margison, GP .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (10) :5828-5837
[18]   Repair-deficient 3-methyladenine DNA glycosylase homozygous mutant mouse cells have increased sensitivity to alkylation-induced chromosome damage and cell killing [J].
Engelward, BP ;
Dreslin, A ;
Christensen, J ;
Huszar, D ;
Kurahara, C ;
Samson, L .
EMBO JOURNAL, 1996, 15 (04) :945-952
[19]  
EVENSEN G, 1982, NATURE, V296, P773, DOI 10.1038/296773a0
[20]   Cytotoxic and mutagenic response of mismatch repair-defective human cancer cells exposed to a food-associated heterocyclic amine [J].
Glaab, WE ;
Skopek, TR .
CARCINOGENESIS, 1999, 20 (03) :391-394