Literature DB >> 1207708

Mutagenicity of dimethylnitrosamine to mammalian cells as determined by the use of mouse liver microsomes.

M Umeda, M Saito.   

Abstract

The mutagenicity of dimethylnitrosamine (DMN) to mammalian cells was investigated using a metabolic activation system. Mutation from 8-azaguanine (8AG) sensitivity to resistance in FM3A cells, a cell line derived from C3H mouse mammary carcinoma, was found only in the presence of dimethylnitrosamine, mouse liver microsomes and cofactors. The different inducibility of the mutation was shown by the use of liver microsomes from different strains of mouse.

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Year:  1975        PMID: 1207708

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


  4 in total

1.  Activation of xenobiotics by monooxygenases: cultures of mammalian cells as analytical tool.

Authors:  F J Wiebel; S Brown; H L Waters; J K Selkirk
Journal:  Arch Toxicol       Date:  1977-12-30       Impact factor: 5.153

2.  Metabolic activation of drugs in mutagenicity tests in vitro.

Authors:  M B Roberfroid
Journal:  Arch Toxicol       Date:  1980-11       Impact factor: 5.153

3.  Monooxygenase and UDP-glucuronyltransferase activities in established cell culture.

Authors:  F J Wiebel; J Singh
Journal:  Arch Toxicol       Date:  1980-03       Impact factor: 5.153

4.  Quantitative studies on the in vitro metabolic activation of dimethylnitrosamine by rat liver postmitochondrial supernatant.

Authors:  D J Doolittle; J I Goodman
Journal:  Environ Health Perspect       Date:  1984-08       Impact factor: 9.031

  4 in total

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