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对已知或疑似人类致癌物产生的基因活性光谱的分析。

An analysis of the spectra of genetic activity produced by known or suspected human carcinogens.

作者信息

Garrett N E, Stack H F, Gross M R, Waters M D

出版信息

Mutat Res. 1984 Sep-Nov;134(2-3):89-111. doi: 10.1016/0165-1110(84)90006-x.

Abstract

For 24 agents classified by the International Agency for Research on Cancer as known or suspected human carcinogens, we previously catalogued the qualitative genetic bioassay data available in the literature. In the present analysis, dose information, where available, was added to this data base: either the lowest effective dose (LED) or the highest ineffective dose (HID) was recorded for each agent and bioassay system. Bioassay systems were organized according to classes of genetic activity and subdivided by the phylogenetic level of the test organism. For each compound, the quantitative results in the test systems were represented by computer-generated bar graphs ('genetic activity spectra'). The x-axis unit values corresponded to the 100 different test systems, and the y-axis values were the logarithmically transformed LED or HID values. Statistical methods and pattern-recognition techniques were used to evaluate the genetic activity spectra. Spectra were compared among agents grouped according to target-organ specificity. In addition, the spectra of all possible pairs of compounds were compared to identify compounds displaying qualitatively or quantitatively similar genetic activity. Chemically similar compounds frequently produced similar spectra of genetic activity, and it was possible to identify the most appropriate test systems for some classes of compounds. As the data base for human carcinogens is enlarged, analysis of genetic activity spectra may contribute to our understanding of the structure-activity relationships and mechanisms of action of these agents.

摘要

对于国际癌症研究机构分类为已知或疑似人类致癌物的24种化学物质,我们之前已整理了文献中可用的定性遗传生物测定数据。在本分析中,若有剂量信息,则将其添加到该数据库中:记录每种化学物质和生物测定系统的最低有效剂量(LED)或最高无效剂量(HID)。生物测定系统根据遗传活性类别进行组织,并按测试生物体的系统发育水平细分。对于每种化合物,测试系统中的定量结果由计算机生成的柱状图(“遗传活性谱”)表示。x轴单位值对应100个不同的测试系统,y轴值为经对数转换的LED或HID值。使用统计方法和模式识别技术来评估遗传活性谱。在根据靶器官特异性分组的化学物质之间比较谱图。此外,比较所有可能的化合物对的谱图,以识别显示定性或定量相似遗传活性的化合物。化学结构相似的化合物通常产生相似的遗传活性谱,并且有可能为某些类别的化合物确定最合适的测试系统。随着人类致癌物数据库的扩大,遗传活性谱分析可能有助于我们理解这些化学物质的构效关系和作用机制。

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