[An in vivo DNA adduct database for carcinogens: O6-alkylguanine, O4-alkylthymine and 8-hydroxyguanine].

K Morimoto, M Kimura, T Murata, Y Imai, N Ookami, T Igarashi, N Kanoh, T Kaminuma, Y Hayashi
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引用次数: 0

Abstract

Many carcinogens react with DNA and form critical DNA adducts, such as O6-alkylguanine (O6-AG), O4-alkylthymine (O4-AT), and 8-hydroxyguanine (8-OHG). This study provides a database that can be used for molecular dosimetry of these DNA adducts. A literature survey on DNA binding in vivo was done by the Dialog search from the MEDLINE database. We propose a Critical Covalent Binding Index (CCBI) for the assessment of in vivo DNA binding level (expressed as micro mol chemical bound per mol G or T/mmol chemical administered per kg body weight). The number of records and compounds in parenthesis of O6-AG, O4-AT, and 8-OHG were 245(13), 54(4), 79(15), respectively. Since the CCBI values for N-nitrosamine in target organ were higher than for non-target organ, they may provide a useful index for estimation of target organ site and carcinogenic potency. As a case example, CCBI values for O4-AT from animal data were applied for diethylnitrosamine human exposure estimation by diethylnitrosamine.

[一个体内DNA加合物数据库:o6 -烷基鸟嘌呤,o4 -烷基胸腺嘧啶和8-羟基鸟嘌呤]。
许多致癌物与DNA发生反应并形成关键的DNA加合物,如o6 -烷基鸟嘌呤(O6-AG)、o4 -烷基胸腺嘧啶(O4-AT)和8-羟基鸟嘌呤(8-OHG)。本研究为这些DNA加合物的分子剂量测定提供了一个数据库。通过MEDLINE数据库中的Dialog搜索,对体内DNA结合的文献进行了调查。我们提出了一个临界共价结合指数(CCBI)来评估体内DNA结合水平(表示为每mol G /微摩尔化学结合或每kg体重/ T/mmol化学结合)。O6-AG、O4-AT和8-OHG的记录数和化合物数分别为245(13)、54(4)、79(15)。由于靶器官中n-亚硝胺的CCBI值高于非靶器官,可为靶器官部位和致癌效力的估计提供有用的指标。作为一个案例,将动物数据中O4-AT的CCBI值应用于二乙基亚硝胺对人类暴露量的估计。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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