Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5860544 | Toxicology Letters | 2013 | 9 Pages |
Abstract
In the present study, a CYP3A4 reporter gene assay, requiring the overexpression of PXR, was used to investigate whether the PAH parent compounds BaP, benzo[c]phenanthrene (BcP) and dibenzo[a,l]pyrene (DBalP) as well as their corresponding phase I metabolites, the respective dihydrodiols and diol epoxides, can induce CYP3A4 promoter activity. BaP, BcP and their dihydrodiols were found to significantly activate the CYP3A4 promoter. Moreover, activation of PXR by all four compounds was detected by using a PXR transactivation assay, supporting that PXR mediates CYP3A4 induction by PAH. Taken together, these results show that both PAH parent compounds as well as their phase I metabolites induce CYP3A4 promoter via the transcription factor PXR.
Keywords
AHR3-methylcholanthreneglutathione S-transferase(s)DNRPXRBenzo[c]phenanthrenePPARγqRT-PCRBAPUASGSTUGTCyPBCPLBDPAHDBDdibenzo[a,l]pyrene3-MCReporter gene assayBenzo[a]pyreneeverted repeatdirect repeatDNA-Binding Domainligand-binding domainupstream activation sequencereal-time quantitative PCRCARPolycyclic aromatic hydrocarbonspolycyclic aromatic hydrocarbon(s)aryl hydrocarbon receptorconstitutive androstane receptorperoxisome proliferator-activated receptor γPregnane X receptor
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Authors
Claudia Luckert, Anke Ehlers, Thorsten Buhrke, Albrecht Seidel, Alfonso Lampen, Stefanie Hessel,