SOS显色试验的化学结构和遗传毒性研究

Volker Mersch-Sundermann , Gilles Klopman , Herbert S. Rosenkranz
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引用次数: 38

摘要

对一个包含461种化学物质的数据库进行了分析,这些化学物质用MULTICASE进行了SOS显色测试,结果建立了一个SAR模型,该模型显示了模型中未包含的化学物质的实验结果和预测结果之间的高度显著一致性(87.3%)。对生物载体及其调节剂性质的分析表明,亲电性和结构特征影响:(a)亲电试剂对DNA亲核位点的可及性;(b) DNA加合物的体积是决定化学物质诱导DNA易出错修复的可能性的因素,如果是这样,则决定这种活性的程度。进一步的分析表明,SOS显色试验与标准(Ames)试验中确定的沙门氏菌突变之间存在显著的机制相似性。
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Chemical structure and genotoxicity: Studies of the SOS chromotest

Analyses of a data base consisting of 461 chemicals tested in the SOS chromotest with MULTICASE resulted in the development of an SAR model that displayed a highly significant concordance (87.3%) between experimental and predicted results of chemicals not included in the model. An analysis of the nature of the biophores and their modulators revealed that electrophilicity and structural features affecting: (a) accessibility of the electrophile to the nucleophilic site on the DNA; and (b) the bulkiness of the DNA adduct were factors determining the probability that a chemical would induce DNA error prone repair and if so the extent of this activity. Additional analyses indicated that there were significant mechanistic similarities between the SOS chromotest and mutations in Salmonella as determined in the standard (‘Ames’) assay.

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DNA adducts and chronic degenerative diseases. Pathogenetic relevance and implications in preventive medicine Carbon tetrachloride: Genetic effects and other modes of action Dr. Hans F. Stich, Professor Emeritus of the University of British Columbia, 1927–1995 Product review Foreword
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