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N-亚硝基化合物的致癌性和致突变性。

Carcinogenicity and mutagenicity of N-nitroso compounds.

作者信息

Lijinsky W

机构信息

NCI-Frederick Cancer Research Facility, LBI-Basic Research Program, Maryland 21701.

出版信息

Mol Toxicol. 1987 Jan-Mar;1(1):107-19.

PMID:3329700
Abstract

The carcinogenic activities in rats and hamsters and the mutagenic activity in Salmonella of a number of N-nitroso compounds belonging to various classes have been compared. While most directly acting N-nitroso compounds and those requiring metabolic activation are mutagenic with appropriate activation and seem to alkylate DNA in vivo, there are exceptions. Some of these are mutagens that are not carcinogenic; others are carcinogens that are nonmutagenic. Even among the mutagenic carcinogens, there is no quantitative relationship between mutagenic and carcinogenic activities. This implies to directly acting compounds and to those requiring metabolic activation. The lack of congruence between the two activities among the nitrosamines is due to the complexity of the metabolic activating processes leading to formation of proximate carcinogens. The deficiencies in the mutagenesis assay appear to arise from a lack of the necessary enzymes in the liver microsomal fractions used for activation. Nitrosamines bearing oxygen on the beta carbon of an alkyl chain are not oxidized by rat microsomal enzymes and hence are not converted to bacterial mutagens by rat liver microsomes. Bacterial mutagenicity is not a guide to carcinogenic activity of N-nitroso compounds or to the mechanisms by which these compounds induce cancer.

摘要

对多种不同类别的N-亚硝基化合物在大鼠和仓鼠中的致癌活性以及在沙门氏菌中的致突变活性进行了比较。虽然大多数直接作用的N-亚硝基化合物以及那些需要代谢活化的化合物在适当活化时具有致突变性,并且似乎在体内使DNA烷基化,但也有例外。其中一些是具有致突变性但无致癌性的物质;另一些是具有致癌性但无致突变性的物质。即使在具有致突变性的致癌物中,致突变活性和致癌活性之间也没有定量关系。这对于直接作用的化合物以及那些需要代谢活化的化合物均适用。亚硝胺类物质中这两种活性之间缺乏一致性是由于导致形成近致癌物的代谢活化过程的复杂性所致。致突变试验中的缺陷似乎源于用于活化的肝微粒体组分中缺乏必要的酶。在烷基链的β碳上带有氧的亚硝胺不会被大鼠微粒体酶氧化,因此不会被大鼠肝脏微粒体转化为细菌诱变剂。细菌致突变性并非N-亚硝基化合物致癌活性或这些化合物诱导癌症机制的指南。

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