International Journal of Molecular Sciences | |
Frederique Bravin1  Radu C. Duca1  Patrick Balaguer2  | |
[1] CEA Saclay, iBiTec-S, SB2SM and URA CNRS 2096, Gif sur Yvette Cedex F-91191, France; E-Mails:;IRCM, Institut de Recherche en Cancérologie de Montpellier, 34298, France; INSERM, U896, Montpellier 34298, France; Université Montpellier 1, Montpellier 34298, France; CRLC Val d’Aurelle Paul Lamarque, 34298, Montpellier, France; E-Mail: | |
关键词: Cytochrome P450; zearalenone; hydroxy-metabolites; estrogenic activities; human; | |
DOI : 10.3390/ijms10041824 | |
来源: mdpi | |
【 摘 要 】
The mycoestrogen zearalenone (ZEN), as well as its reduced metabolites, which belong to the endocrine disruptor bio-molecule family, are substrates for various enzymes involved in steroid metabolism. In addition to its reduction by the steroid dehydrogenase pathway, ZEN also interacts with hepatic detoxification enzymes, which convert it into hydroxylated metabolites (OH-ZEN). Due to their structures to that of estradiol, ZEN and its derived metabolites bind to the estrogen receptors and are involved in endocrinal perturbations and are possibly associated with estrogen-dependent cancers. The primary aim of this present study was to identify the enzymatic cytochrome P450 isoforms responsible for the formation of the most abundant OH-ZEN. We thus studied its
【 授权许可】
CC BY
© 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland.
【 预 览 】
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RO202003190057085ZK.pdf | 226KB | download |