Literature DB >> 34091723

N-vinyl compounds: studies on metabolism, genotoxicity, carcinogenicity.

F Oesch1, N Honarvar2, E Fabian2, F I Berger3, Robert Landsiedel4.   

Abstract

Several N-vinyl compounds are produced in high volumes and are widely employed in the production of copolymers and polymers used in chemical, pharmaceutical, cosmetic and food industry. Hence, information on their genotoxicity and carcinogenicity is requisite. This review presents hitherto available information on the carcinogenicity and genotoxicity of N-vinyl compounds as well as their metabolism potentially generating genotoxic and carcinogenic derivatives. The genotoxicity and carcinogenicity of the investigated N-vinyl compounds vary widely from no observed carcinogenicity tested in lifetime bioassays in two rodent species (up to very high doses) to carcinogenicity in rats at very low doses in the absence of apparent genotoxicity. Despite of the presence of the vinyl group potentially metabolized to an epoxide followed by covalent binding to DNA, genotoxicity was observed for only one of the considered N-vinyl compounds, N-vinyl carbazole. Carcinogenicity was investigated only for two, of which one, N-vinyl pyrrolidone was carcinogenic (but not genotoxic) and ranitidine was neither carcinogenic nor genotoxic. As far as investigated, neither a metabolically formed epoxide nor a therefrom derived diol has been reported for any of the considered N-vinyl compounds. It is concluded that the information collected in this review will further the understanding of the carcinogenic potentials of N-vinyl compounds and may eventually allow approaching their prediction and prevention. A suggestion how to prevent genotoxicity in designing of N-vinyl compounds is presented. However, the available information is scarce and further research especially on the metabolism of N-vinyl compounds is highly desirable.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Carcinogenicity; Genotoxicity; Liver; N-vinyl compounds; Xenobiotic metabolism

Mesh:

Substances:

Year:  2021        PMID: 34091723     DOI: 10.1007/s00204-021-03081-5

Source DB:  PubMed          Journal:  Arch Toxicol        ISSN: 0340-5761            Impact factor:   5.153


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2.  Histamine-2-receptor antagonists and oesophageal cancer.

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3.  Genotoxicity of nitrosated ranitidine.

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Journal:  Mutat Res       Date:  1989-09       Impact factor: 2.433

4.  DNA cross-links in human leucocytes treated with vinyl acetate and acetaldehyde in vitro.

Authors:  B Lambert; Y Chen; S M He; M Sten
Journal:  Mutat Res       Date:  1985-11       Impact factor: 2.433

5.  Performance of 181 chemicals in a Drosophila assay predominantly monitoring interchromosomal mitotic recombination.

Authors:  E W Vogel; M J Nivard
Journal:  Mutagenesis       Date:  1993-01       Impact factor: 3.000

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