Literature DB >> 1001292

Assaying potential carcinogens with Drosophila.

F H Sobels, E Vogel.   

Abstract

Drosophila offers many advantages for the detection of mutagenic activity of carcinogenic agents. It provides the quickest assay system for detecting mutations in animals today. Its generation time is short, and Drosophila is cheap and easy to breed in large numbers. The simple genetic testing methods give unequivocal answers about the whole spectrum of relevant genetic damage. A comparison of the detection capacity of assays sampling different kinds of genetic damage revealed that various substances are highly effective in inducing mutations but do not produce chromosome breakage effects at all, or only at much higher concentrations than those required for mutation induction. Of the different assay systems available, the classical sex-linked recessive lethal test deserves priority, in view of its superior capacity to detect mutagens. Of practical importance is also its high sensitivity, because a large number of loci in one fifth of the genome is tested for newly induced forward mutations, including small deletions. The recent findings that Drosophila is capable of carrying out the same metabolic activation reactions as the mammalian liver makes the organism eminently suitable for verifying results obtained in prescreening with fast microbial assay systems. An additional advantage in this respect is the capacity of Drosophila for detecting short-lived activation products, because intracellular metabolic activation appears to occur within the spermatids and spermatocytes.

Entities:  

Mesh:

Substances:

Year:  1976        PMID: 1001292      PMCID: PMC1475152          DOI: 10.1289/ehp.7615141

Source DB:  PubMed          Journal:  Environ Health Perspect        ISSN: 0091-6765            Impact factor:   9.031


  18 in total

1.  ETHYLATION VERSUS METHYLATION IN MUTATION OF ESCHERICHIA COLI AND DROSOPHILA.

Authors:  T ALDERSON
Journal:  Nature       Date:  1964-09-26       Impact factor: 49.962

2.  Mutagenic activity of the alkaloid heliotrine in Drosophila.

Authors:  A M CLARK
Journal:  Nature       Date:  1959-03-14       Impact factor: 49.962

3.  [STUDIES ON THE MUTAGENIC EFFECT OF VARIOUS NITROSAMINE AND NITROSAMIDE COMPOUNDS].

Authors:  L PASTERNAK
Journal:  Arzneimittelforschung       Date:  1964-07

4.  [Studies on the mutagenic effect of nitrosamines and nitrosomethylurea].

Authors:  L PASTERNAK
Journal:  Acta Biol Med Ger       Date:  1963

5.  Comparative investigations on the chemical induction of point mutations and dominant lethal mutations in mice.

Authors:  P Propping; G Röhrborn; W Buselmaier
Journal:  Mol Gen Genet       Date:  1972

Review 6.  The advantages of drosophila for mutation studies.

Authors:  F H Sobels
Journal:  Mutat Res       Date:  1974-08       Impact factor: 2.433

7.  Mutagenicity of hycanthone in Drosophila melanogaster.

Authors:  A G Knaap; P G Kramers
Journal:  Mutat Res       Date:  1974-01       Impact factor: 2.433

8.  [Organotropic carcinogenic effects of 65 various N-nitroso- compounds on BD rats].

Authors:  H Druckrey; R Preussmann; S Ivankovic; D Schmähl
Journal:  Z Krebsforsch       Date:  1967

Review 9.  Evaluation of short-term tests for carcinogenicity.

Authors:  D R Stoltz; L A Poirier; C C Irving; H F Stich; J H Weisburger; H C Grice
Journal:  Toxicol Appl Pharmacol       Date:  1974-08       Impact factor: 4.219

10.  Effect of storage of alkylated chromosomes on the mutagenic effectiveness of monofunctional alkylation.

Authors:  A H Khan
Journal:  Mutat Res       Date:  1969 Nov-Dec       Impact factor: 2.433

View more
  2 in total

Review 1.  Drosophotoxicology: the growing potential for Drosophila in neurotoxicology.

Authors:  Matthew D Rand
Journal:  Neurotoxicol Teratol       Date:  2009-06-24       Impact factor: 3.763

2.  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
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.