Literature DB >> 31845612

Cancer Hazard Identification Integrating Human Variability: The Case of Coumarin.

ChingYi Jennifer Hsieh1, Meng Sun1, Gwendolyn Osborne1, Karin Ricker1, Feng C Tsai1, Kate Li1, Rajpal Tomar1,2, Jimmy Phuong3, Rose Schmitz1, Martha S Sandy1.   

Abstract

Coumarin is a naturally occurring sweet-smelling benzopyrone that may be extracted from plants or synthesized for commercial uses. Its uses include as a flavoring agent, fragrance enhancer, and odor-masking additive. We reviewed and evaluated the scientific evidence on the carcinogenicity of coumarin, integrating information from carcinogenicity studies in animals with mechanistic and other relevant data, including data from toxicogenomic, genotoxicity, and metabolism studies, and studies of human variability of a key enzyme, CYP2A6. Increases in tumors were observed in multiple studies in rats and mice in multiple tissues. Our functional pathway analysis identified several common cancer-related biological processes/pathways affected by coumarin in rat liver following in vivo exposure and in human primary hepatocytes exposed in vitro. When coumarin 7-hydroxylation by CYP2A6 is compromised, this can lead to a shift in metabolism to the 3,4-epoxidation pathway and increased generation of electrophilic metabolites. Mechanistic data align with 3 key characteristics of carcinogens, namely formation of electrophilic metabolites, genotoxicity, and induction of oxidative stress. Considerations of metabolism, human variability in CYP2A6 activity, and coumarin hepatotoxicity in susceptible individuals provide additional support for carcinogenicity concern. Our analysis illustrates the importance of integrating information on human variability in the cancer hazard identification process.

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Keywords:  CYP2A6 polymorphisms; human variability; carcinogenicity; coumarin; electrophilic; genotoxicity; key characteristics of carcinogens; metabolism; oxidative stress; toxicogenomics

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Year:  2019        PMID: 31845612     DOI: 10.1177/1091581819884544

Source DB:  PubMed          Journal:  Int J Toxicol        ISSN: 1091-5818            Impact factor:   2.032


  1 in total

1.  A fast and reliable method for monitoring genomic instability in the model organism Caenorhabditis elegans.

Authors:  Merle Marie Nicolai; Barbara Witt; Andrea Hartwig; Tanja Schwerdtle; Julia Bornhorst
Journal:  Arch Toxicol       Date:  2021-08-30       Impact factor: 5.153

  1 in total

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