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DNA加合物研究在癌症分子剂量测定和风险评估动物模型中的意义。

Significance of DNA adduct studies in animal models for cancer molecular dosimetry and risk assessment.

作者信息

Beland F A, Poirier M C

机构信息

National Center for Toxicological Research, Jefferson, AR 72079.

出版信息

Environ Health Perspect. 1993 Mar;99:5-10. doi: 10.1289/ehp.93995.

Abstract

To elucidate the relationship between DNA adduct formation and tumorigenesis, a number of experiments have been conducted to measure DNA adducts in target tissues from experimental animals during continuous exposure to carcinogens. With aflatoxins, aromatic amines, and polycyclic aromatic hydrocarbons, tumor induction appears to be associated with the major DNA adduct detected, whereas with N-nitrosamines the response is normally correlated with minor forms of DNA damage. During continuous carcinogen administration, steady-state adduct concentrations are generally obtained in the target tissues, and there is often a linear correlation between the carcinogen concentration and the steady-state DNA adduct level. Exceptions exist when the mechanism of activation changes or with the onset of significant toxicity. Steady-state DNA adduct levels are often linearly related to the tumorigenic response. Carcinogen-induced cell proliferation occurs when significant deviations from linearity are observed. Because DNA adducts detected in humans are chemically identical to those found in experimental animals, DNA adduct data in animals may contribute to our understanding of human cancer risk.

摘要

为阐明DNA加合物形成与肿瘤发生之间的关系,已开展了多项实验,以测量实验动物在持续接触致癌物期间靶组织中的DNA加合物。对于黄曲霉毒素、芳香胺和多环芳烃,肿瘤诱导似乎与检测到的主要DNA加合物有关,而对于N-亚硝胺,反应通常与DNA损伤的次要形式相关。在持续给予致癌物期间,通常在靶组织中获得稳态加合物浓度,并且致癌物浓度与稳态DNA加合物水平之间通常存在线性相关性。当激活机制发生变化或出现明显毒性时会出现例外情况。稳态DNA加合物水平通常与致瘤反应呈线性相关。当观察到明显偏离线性时,会发生致癌物诱导的细胞增殖。由于在人类中检测到的DNA加合物与在实验动物中发现的化学性质相同,动物中的DNA加合物数据可能有助于我们了解人类癌症风险。

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