DNA Alkylation Damage by Nitrosamines and Relevant DNA Repair Pathways

被引:29
|
作者
Fahrer, Joerg [1 ]
Christmann, Markus [2 ]
机构
[1] RPTU Kaiserslautern Landau, Dept Chem, Div Food Chem & Toxicol, Erwin Schrodinger Str 52, D-67663 Kaiserslautern, Germany
[2] Univ Med Ctr Mainz, Dept Toxicol, Obere Zahlbacher Str 67, D-55131 Mainz, Germany
关键词
N-nitroso compounds; N-nitrosamines; DNA alkylation; DNA damage; DNA repair; MGMT; AAG; ALKBH; BER; NER; TLS; BASE EXCISION-REPAIR; HUMAN O-6-METHYLGUANINE-DNA METHYLTRANSFERASE; TOBACCO-SPECIFIC NITROSAMINES; POLY(ADP-RIBOSE) PAR POLYMER; MGMT PROMOTER METHYLATION; ERROR-FREE REPLICATION; DOUBLE-STRAND BREAKS; N-NITROSO COMPOUNDS; TRANSLESION SYNTHESIS; IN-VIVO;
D O I
10.3390/ijms24054684
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
Nitrosamines occur widespread in food, drinking water, cosmetics, as well as tobacco smoke and can arise endogenously. More recently, nitrosamines have been detected as impurities in various drugs. This is of particular concern as nitrosamines are alkylating agents that are genotoxic and carcinogenic. We first summarize the current knowledge on the different sources and chemical nature of alkylating agents with a focus on relevant nitrosamines. Subsequently, we present the major DNA alkylation adducts induced by nitrosamines upon their metabolic activation by CYP450 monooxygenases. We then describe the DNA repair pathways engaged by the various DNA alkylation adducts, which include base excision repair, direct damage reversal by MGMT and ALKBH, as well as nucleotide excision repair. Their roles in the protection against the genotoxic and carcinogenic effects of nitrosamines are highlighted. Finally, we address DNA translesion synthesis as a DNA damage tolerance mechanism relevant to DNA alkylation adducts.
引用
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页数:34
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