QSARS of mutagens and carcinogens: Two case studies illustrating problems in the construction of models for noncongeneric chemicals

Romualdo Benigni , Ann M. Richard
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引用次数: 45

Abstract

There is a strong motivation to develop QSAR models for toxicity prediction for use in screening, for setting testing priorities, and for reducing reliance on animal testing. Decisions must be made daily by toxicologists in governments and industry to direct limited testing resources to the most urgent public health problems, and to direct the types of chemical synthesis and product development efforts undertaken. This need has motivated attempts to construct general QSAR models (e.g., for rodent carcinogenicity), not tailored to congeneric series of chemicals. These various attempts have provided interesting and important scientific evidence; however, they have also shared a limited overall performance. The goal of this paper is to illustrate, by two unrelated actual examples of QSARs for mutagens and carcinogens, some fundamental problems relative to the application of general QSAR approaches to noncongeneric chemicals. Both examples consider data sets that are noncongeneric in a chemical structure and mechanism of action sense: in the first case, a mean mutagenic potency defined as an average over multiple genetic toxicity endpoints, and, in the second case, the NTP two-sexes, two species rodent carcinogenicity bioassay results for 280 carcinogens and noncarcinogens. The problems encountered with the QSAR analyses of these two cases indicate that a successful approach to the problem of QSAR modeling of noncongeneric data will need to consider the multidimensional nature of the problem in both a chemical and a biological sense. Since different chemical classes represent largely independent action mechanisms, some means for extracting local QSARs for constituent classes will be necessary. Alternatively, a general QSAR derived for a noncongeneric data set will need to be scrutinized and decomposed along chemical class lines in order establish boundaries for application and confidence levels for prediction.

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诱变剂和致癌物的QSARS:两个案例研究说明了在构建非同源化学品模型中的问题
有强烈的动机开发QSAR模型用于毒性预测,用于筛选,确定测试优先级,并减少对动物试验的依赖。政府和工业界的毒理学家必须每天作出决定,将有限的测试资源用于最紧迫的公共卫生问题,并指导所进行的化学合成和产品开发工作的类型。这种需求促使人们尝试构建通用的QSAR模型(例如,啮齿动物致癌性),而不是针对同类系列的化学品。这些不同的尝试提供了有趣而重要的科学证据;然而,它们的整体表现也有限。本文的目的是通过两个不相关的用于诱变剂和致癌物质的QSAR的实际例子来说明与一般QSAR方法应用于非同源化学品有关的一些基本问题。这两个例子都考虑了在化学结构和作用机制意义上不相同的数据集:在第一个案例中,平均诱变效力定义为多个遗传毒性终点的平均值,在第二个案例中,NTP对280种致癌物和非致癌物的两性、两种啮齿动物致癌性生物测定结果。对这两个案例进行QSAR分析时遇到的问题表明,要想成功地解决非同类数据的QSAR建模问题,需要在化学和生物学意义上考虑问题的多维性质。由于不同的化学类别代表了很大程度上独立的作用机制,因此需要一些方法来提取组成类别的局部qsar。或者,为非同类数据集导出的一般QSAR将需要沿着化学类线进行仔细检查和分解,以便为预测的应用和置信水平建立界限。
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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