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1
Aspects of database construction and interrogation of relevance to the accurate prediction of rodent carcinogenicity and mutagenicity.与准确预测啮齿动物致癌性和致突变性相关的数据库构建及查询方面。
Environ Health Perspect. 1991 Dec;96:97-100. doi: 10.1289/ehp.919697.
2
The influence of chemical structure on the extent and sites of carcinogenesis for 522 rodent carcinogens and 55 different human carcinogen exposures.522种啮齿动物致癌物和55种不同人类致癌物暴露的化学结构对致癌作用范围和部位的影响。
Mutat Res. 1993 Mar;286(1):3-74. doi: 10.1016/0027-5107(93)90003-x.
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Examples of uses of databases for quantitative and qualitative correlation studies between genotoxicity and carcinogenicity.用于遗传毒性与致癌性之间定量和定性相关性研究的数据库应用实例。
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The results of assays in Drosophila as indicators of exposure to carcinogens.果蝇检测结果作为接触致癌物指标的情况。
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Mouse-specific carcinogens: an assessment of hazard and significance for validation of short-term carcinogenicity bioassays in transgenic mice.小鼠特异性致癌物:对转基因小鼠短期致癌性生物测定验证的危害及意义评估
Hum Exp Toxicol. 1998 Apr;17(4):193-205. doi: 10.1177/096032719801700401.
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Are genotoxic carcinogens more potent than nongenotoxic carcinogens?基因毒性致癌物比非基因毒性致癌物更具致癌性吗?
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The genetic toxicity database of the National Toxicology Program: evaluation of the relationships between genetic toxicity and carcinogenicity.国家毒理学计划的遗传毒性数据库:遗传毒性与致癌性之间关系的评估
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Integrated approach to testing and assessment for predicting rodent genotoxic carcinogenicity.用于预测啮齿动物遗传毒性致癌性的测试与评估综合方法。
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Evaluation of the ability of a battery of three in vitro genotoxicity tests to discriminate rodent carcinogens and non-carcinogens II. Further analysis of mammalian cell results, relative predictivity and tumour profiles.一组三项体外遗传毒性试验鉴别啮齿类致癌物和非致癌物能力的评估II. 哺乳动物细胞结果、相对预测性及肿瘤谱的进一步分析
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本文引用的文献

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Prediction of chemical carcinogenicity in rodents from in vitro genetic toxicity assays.通过体外遗传毒性试验预测啮齿动物的化学致癌性。
Science. 1987 May 22;236(4804):933-41. doi: 10.1126/science.3554512.
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Structural alerts to genotoxicity: the interaction of human and artificial intelligence.
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Classification according to chemical structure, mutagenicity to Salmonella and level of carcinogenicity of a further 39 chemicals tested for carcinogenicity by the U.S. National Toxicology Program.根据化学结构、对沙门氏菌的致突变性以及美国国家毒理学计划测试的另外39种化学物质的致癌性水平进行分类。
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The Genetic Activity Profile database.基因活性谱数据库。
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5
The Carcinogenic Potency Database: analyses of 4000 chronic animal cancer experiments published in the general literature and by the U.S. National Cancer Institute/National Toxicology Program.致癌强度数据库:对发表于普通文献以及美国国立癌症研究所/国家毒理学计划的4000项慢性动物癌症实验的分析。
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6
Definitive relationships among chemical structure, carcinogenicity and mutagenicity for 301 chemicals tested by the U.S. NTP.美国国家毒理学计划(NTP)测试的301种化学物质的化学结构、致癌性和致突变性之间的确切关系。
Mutat Res. 1991 May;257(3):229-306. doi: 10.1016/0165-1110(91)90003-e.

与准确预测啮齿动物致癌性和致突变性相关的数据库构建及查询方面。

Aspects of database construction and interrogation of relevance to the accurate prediction of rodent carcinogenicity and mutagenicity.

作者信息

Ashby J

机构信息

ICI Central Toxicology Laboratory, Alderley Park, Cheshire, UK.

出版信息

Environ Health Perspect. 1991 Dec;96:97-100. doi: 10.1289/ehp.919697.

DOI:10.1289/ehp.919697
PMID:1820286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1568228/
Abstract

Attempts to reconcile qualitative carcinogenicity databases with qualitative mutagenicity database continue to indicate that there is no useful relationship between mutagenicity/genotoxicity and rodent carcinogenicity. It is suggested that recognition of two classes of carcinogen, genotoxic and nongenotoxic, is the first step in finding meaningful correlations between the above parameters. This then leads to purposeful intervention into the databases, including rejecting low quality data, abandoning some assays from the database, and clustering certain end points as repetitive rather that independent of each other. Seeking specific correlations within a focused database may yield knowledge from the current wealth of information. The effort required to build databases, particularly quantitative ones, has so far prevented the equally arduous task of their correct interrogation. Preliminary indications are the mutagenicity is closely correlated with genotoxic carcinogenesis and completely independent of nongenotoxic carcinogenesis.

摘要

将定性致癌性数据库与定性致突变性数据库进行比对的尝试不断表明,致突变性/基因毒性与啮齿动物致癌性之间不存在有用的关联。有人提出,认识到两类致癌物,即基因毒性致癌物和非基因毒性致癌物,是在上述参数之间找到有意义关联的第一步。这进而导致对数据库进行有目的的干预,包括剔除低质量数据、从数据库中舍弃一些检测方法,以及将某些终点归为重复性而非相互独立的类别。在一个重点突出的数据库内寻找特定关联,可能会从当前丰富的信息中获取知识。迄今为止,构建数据库,尤其是定量数据库所需的努力阻碍了对其进行同样艰巨的正确查询任务。初步迹象表明,致突变性与基因毒性致癌作用密切相关,而与非基因毒性致癌作用完全无关。