Literature DB >> 3331692

Performance of short-term tests for detection of human carcinogens.

T Kuroki1, T Matsushima.   

Abstract

The performance of short-term tests for detection of carcinogens has been validated by several investigators and international collaborative programmes. A large number of chemicals have been tested by the Salmonella/microsome assay and high values of sensitivity and specificity, often greater than 70%, were reported. For 71 human carcinogens classified in Groups 1, 2A and 2B by the International Agency for Research on Cancer (IARC), the Salmonella/microsome test showed a sensitivity of 62.1%: 36 were positive out of 58 chemicals tested. Similar or rather higher values were obtained with Escherichia coli mutation assay (72.0%, 18/25), mutation assays in fungi (78.9%, 30/38), mutation assays in insects (65.7%, 23/35), and assays measuring DNA damage in prokaryotes (80.5%, 33/41). In assays using mammalian cells, tests on chromosomal anomaly showed a relatively high sensitivity: 61.7% (29/47) in chromosomal structural aberration assays and 80.6% (25/31) in sister chromatid exchange (SCE) assays. Comparable values were also obtained in mutation assays of mammalian cells (73.0%, 27/37) and cell transformation assays (87.5%, 21/24). Results of monitoring of exposed populations did not necessarily show a high sensitivity to human carcinogens (44.4%, 12/27). Human carcinogen data were further analysed in order to find a combination of tests which may increase the predictive value. Among human carcinogens, 17 chemicals are not mutagenic in the Salmonella/microsome assay. Although 9 of 17 chemicals (asbestos, hormones, chlorinated compounds and 1,4-dioxane) were not positive in any short-term assays, some gave positive results in a variety of assays, e.g. arsenic and benzene were positive in assays of chromosomal anomaly in mammalian cells in vitro. Combinations of the Salmonella/microsome assay with certain tests using mammalian cells were found to increase the sensitivity significantly. Chromosomal anomaly assays of mammalian cells in vitro seem to be most relevant for detection of human carcinogens when used in combination with the Salmonella/microsome assay.

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Year:  1987        PMID: 3331692     DOI: 10.1093/mutage/2.1.33

Source DB:  PubMed          Journal:  Mutagenesis        ISSN: 0267-8357            Impact factor:   3.000


  5 in total

1.  Prevalence of genotoxic chemicals among animal and human carcinogens evaluated in the IARC Monograph Series.

Authors:  H Bartsch; C Malaveille
Journal:  Cell Biol Toxicol       Date:  1989-06       Impact factor: 6.691

2.  Effects of selenium on the structure and function of recombinant human S-adenosyl-L-methionine dependent arsenic (+3 oxidation state) methyltransferase in E. coli.

Authors:  Zhirong Geng; Xiaoli Song; Zhi Xing; Jinlong Geng; Sichun Zhang; Xinrong Zhang; Zhilin Wang
Journal:  J Biol Inorg Chem       Date:  2009-01-22       Impact factor: 3.358

3.  Residues in human arsenic (+3 oxidation state) methyltransferase forming potential hydrogen bond network around S-adenosylmethionine.

Authors:  Xiangli Li; Jing Cao; Shuping Wang; Zhirong Geng; Xiaoli Song; Xin Hu; Zhilin Wang
Journal:  PLoS One       Date:  2013-10-04       Impact factor: 3.240

4.  Identification of the third binding site of arsenic in human arsenic (III) methyltransferase.

Authors:  Xiangli Li; Zhirong Geng; Jiayin Chang; Shuping Wang; Xiaoli Song; Xin Hu; Zhilin Wang
Journal:  PLoS One       Date:  2013-12-31       Impact factor: 3.240

5.  Predicting carcinogenicity by using batteries of dependent short-term tests.

Authors:  B S Kim; B H Margolin
Journal:  Environ Health Perspect       Date:  1994-01       Impact factor: 9.031

  5 in total

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