Literature DB >> 6413857

The sex-linked recessive lethal test for mutagenesis in Drosophila melanogaster. A report of the U.S. Environmental Protection Agency Gene-Tox Program.

W R Lee, S Abrahamson, R Valencia, E S von Halle, F E Würgler, S Zimmering.   

Abstract

The test for sex-linked recessive lethals (SLRL) in Drosophila melanogaster has been used to detect induced mutations since 1927. The advantage of the test for both screening and hazard evaluation is its objectivity in testing for transmissible mutations in the germ cells of a eukaryote. Statistical criteria for both positive and negative mutagenicity at the highest concentration tested under a particular exposure condition were developed by the Work Group, and a recommended protocol for future testing was agreed upon. For 421 compounds there were sufficient data available in the literature for analysis; 198 compounds were found to be positive and 46 negative at the highest concentration tested. Most experiments had been done for objectives of pure research rather than for deliberately screening for mutagenicity, although many of the 421 chemicals were selected for testing because of suspected mutagenicity. Therefore, the statement of 198 positive and 46 negative should not be taken as an example of the proportion of mutagens in the environment. In three sets of experiments with D. melanogaster that were done specifically for screening, one involving 40 compounds for the Environmental Protection Agency (EPA), the others involving 13 for the Food and Drug Administration (FDA), only 6 mutagens were discovered. After completion of the classification of compounds according to their response in the SLRL test, the compounds were classified as to their carcinogenic response according to the list of Griesemer and Cueto (1980). There were 62 compounds that could be classified as positive or negative for both carcinogenesis and mutagenesis. Of the 62 compounds, there was agreement between the carcinogenesis and mutagenesis classification in 56 (50 positive and 6 negative), or 90% would have been correctly classified as to carcinogenesis from only the SLRL test. Because of inadequate sample size, 177 compounds could not be classified as positive or negative according to the statistical criteria established by the Work Group. This large number of inadequately tested compounds reflects the fact that many of the experiments were not done for screening. Further work is needed on the compounds with inadequate sample size.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1983        PMID: 6413857     DOI: 10.1016/0165-1110(83)90025-8

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  11 in total

Review 1.  Models of germ cell development and their application for toxicity studies.

Authors:  Daniel W Ferreira; Patrick Allard
Journal:  Environ Mol Mutagen       Date:  2015-03-28       Impact factor: 3.216

2.  Mapping a mutator, mu2, which increases the frequency of terminal deletions in Drosophila melanogaster.

Authors:  M Wang; L E Champion; H Biessmann; J M Mason
Journal:  Mol Gen Genet       Date:  1994-12-01

3.  Mutagenicity testing with Drosophila.

Authors:  F E Würgler
Journal:  Arch Toxicol       Date:  1980-11       Impact factor: 5.153

4.  Aristolochic acid is mutagenic and recombinogenic in Drosophila genotoxicity tests.

Authors:  H Frei; F E Würgler; H Juon; C B Hall; U Graf
Journal:  Arch Toxicol       Date:  1985-01       Impact factor: 5.153

Review 5.  Invertebrates in testing of environmental chemicals: are they alternatives?

Authors:  L Lagadic; T Caquet
Journal:  Environ Health Perspect       Date:  1998-04       Impact factor: 9.031

6.  In vitro studies on the metabolism of aflatoxin B1 and aldrin in testes of genetically different strains of Drosophila melanogaster.

Authors:  R E Foerster; F E Würgler
Journal:  Arch Toxicol       Date:  1984-11       Impact factor: 5.153

7.  Genotoxic evaluation of ten carcinogens in the Drosophila melanogaster wing spot test.

Authors:  M Batiste-Alentorn; N Xamena; A Creus; R Marcos
Journal:  Experientia       Date:  1995-01-15

Review 8.  A Novel Strategy to Predict Carcinogenicity of Antiparasitics Based on a Combination of DNA Lesions and Bacterial Mutagenicity Tests.

Authors:  Qianying Liu; Zhixin Lei; Feng Zhu; Awais Ihsan; Xu Wang; Zonghui Yuan
Journal:  Front Public Health       Date:  2017-11-09

9.  QSAR models for reproductive toxicity and endocrine disruption in regulatory use--a preliminary investigation.

Authors:  G E Jensen; J R Niemelä; E B Wedebye; N G Nikolov
Journal:  SAR QSAR Environ Res       Date:  2008       Impact factor: 3.000

10.  Protective effects of tea polyphenols and β-carotene against γ-radiation induced mutation and oxidative stress in Drosophila melanogaster.

Authors:  Isha Nagpal; Suresh K Abraham
Journal:  Genes Environ       Date:  2017-11-01
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