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Shifted concentration dependency of EpRE- and XRE-mediated gene expression points at monofunctional EpRE-mediated induction by flavonoids at physiologically relevant concentrations.

Authors :
Lee-Hilz YY
ter Borg S
van Berkel WJ
Rietjens IM
Aarts JM
Source :
Toxicology in vitro : an international journal published in association with BIBRA [Toxicol In Vitro] 2008 Jun; Vol. 22 (4), pp. 921-6. Date of Electronic Publication: 2008 Jan 26.
Publication Year :
2008

Abstract

Flavonoids are important bioactive compounds, omnipresent in the human diet, and are reported to be bifunctional inducers. These phytochemicals are able to induce xenobiotic-responsive element (XRE)- and electrophile-responsive element (EpRE)-mediated gene expression, resulting in the induction of biotransformation enzymes. To test whether flavonoid-induced EpRE-mediated gene expression could be the result of upstream XRE-mediated gene expression, several flavonoids were tested for their ability to induce XRE- and EpRE-mediated gene expression using two stably transfected reporter gene cell lines constructed in the same mouse Hepa-1c1c7 hepatoma background. Although classified as bifunctional inducers, all flavonoids were found to induce EpRE- and XRE-mediated gene expression in a different concentration range, which presents an issue not considered by the current definition of a bifunctional inducer. At physiological relevant concentrations, the induction of gene expression via the EpRE transcriptional enhancer element is dominant, leading in particular to elevated levels of EpRE-regulated detoxifying enzymes. Furthermore, these results strongly suggest that EpRE-mediated gene expression induced by flavonoids is not a downstream reaction of XRE-mediated gene expression.

Details

Language :
English
ISSN :
0887-2333
Volume :
22
Issue :
4
Database :
MEDLINE
Journal :
Toxicology in vitro : an international journal published in association with BIBRA
Publication Type :
Academic Journal
Accession number :
18314304
Full Text :
https://doi.org/10.1016/j.tiv.2008.01.008