DNA-ADDUCTS OF CHEMICAL CARCINOGENS
DNA-ADDUCTS OF CHEMICAL CARCINOGENS
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DOI:
10.1093/carcin/16.3.437
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发表时间:
1995-03-01
期刊:
影响因子:
4.7
通讯作者:
DIPPLE, A
中科院分区:
文献类型:
--
作者:
DIPPLE, A
During the 30 years or so following the identification of the first pure chemical carcinogen (1), no common factors or pathways in the mechanism of action of carcinogens from different chemical classes were evident. For this reason perhaps, each class of carcinogen, eg the polycyclic aromatic hydrocarbons, the aromatic amines and the nitrosamines, was often reviewed and discussed separately. The discovery by the Millers and their colleagues of the role of metabolism in carcinogen activation (2) revealed a commonality amongst many carcinogens, ie a chemical reactivity towards cellular macromolecules, such as DNA (3, 4). Today, DNA adduct formation is recognized as a common property of most potent carcinogens and the formation of such adducts is the basis of several current strategies in molecular epidemiology and biomonitoring. Despite this common aspect of mechanism for many chemical carcinogens, the complexities of metabolic activation and of the chemistry and stereochemistry of adduct formation have tended to keep some degree of compartmentalization in research and in literature reviews of DNA adduct formation by different classes of chemical compounds (5).In this article, an attempt is made to summarize carcinogen adduct formation in a fashion that emphasizes features that are common to different chemical classes. This perspective is achieved by classifying chemical carcinogens on the basis of the chemistry of DNA adduct formation in aqueous solution rather than on chemical structure. Adopting this approach, the major division of chemical carcinogens into those intrinsically reactive towards DNA, such as alkylating agents, and those requiring metabolic activation, such as nitrosamines for. example, disappears. While mechanisms of metabolic activation remain important concerns, alkylation-of-DNA is the chemical mechanism through which both types of agent, exemplified above, form adducts with DNA. Indeed, examination of the literature on adduct formation {reviewed in 5}, indicates that the majority of known carcinogens react with DNA through one of only three general types of chemical reaction. These involve the transfer to DNA of either:(i) an alkyl residue;(ii) an arylamine residue; or (iii) an aralkyl residue.