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大鼠和小鼠致癌潜能比较中的一些同义反复方面。

Some tautologous aspects of the comparison of carcinogenic potency in rats and mice.

作者信息

Bernstein L, Gold L S, Ames B N, Pike M C, Hoel D G

出版信息

Fundam Appl Toxicol. 1985 Feb;5(1):79-86. doi: 10.1016/0272-0590(85)90051-x.

Abstract

In risk estimation, the results of rodent carcinogenesis experiments are often used to quantitatively predict effects in man. The justification for this approach has in large part been dependent upon the good correlation of carcinogenic potency found between mice and rats over large numbers of test chemicals. Using the data base of chemicals tested by the NCI Bioassay Program, we observe that there is a very high correlation of the maximum doses tested (max-d) for rats and mice on a milligram per kilogram body weight per day basis. Next we show that the calculated carcinogenic potency (b-defined in the paper) is restricted to an approximately 30-fold range surrounding log(2)/max-d, which has a biological as well as a statistical basis. Since the max-d's for the set of NCI test chemicals vary over many orders of magnitude, it necessarily follows statistically that the carcinogenic potencies will be highly correlated. This "artifact" of potency estimation does not imply that there is no basis for extrapolating animal results to man. It does suggest, however, that the interpretation of correlation studies of carcinogenic potency needs much further thought.

摘要

在风险评估中,啮齿动物致癌实验的结果常被用于定量预测对人类的影响。这种方法的合理性在很大程度上依赖于在大量测试化学品中发现的小鼠和大鼠之间致癌效力的良好相关性。利用美国国立癌症研究所生物测定项目测试的化学品数据库,我们观察到,以每日每千克体重毫克数为基础,大鼠和小鼠的最大测试剂量(max-d)之间存在非常高的相关性。接下来我们表明,计算出的致癌效力(本文中定义为b)被限制在围绕log(2)/max-d的大约30倍范围内,这有生物学和统计学基础。由于美国国立癌症研究所测试化学品组的max-d在多个数量级上变化,从统计学上必然得出致癌效力将高度相关。这种效力评估的“假象”并不意味着没有将动物实验结果外推至人类的依据。然而,这确实表明,对致癌效力相关性研究的解释需要更多深入思考。

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