Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/70631
標題: Fucoxanthin Attenuates Rifampin-Induced Cytochrome P450 3A4 (CYP3A4) and Multiple Drug Resistance 1 (MDR1) Gene Expression Through Pregnane X Receptor (PXR)-Mediated Pathways in Human Hepatoma HepG2 and Colon Adenocarcinoma LS174T Cells
作者: Liu, C.L.
Lim, Y.P.
Hu, M.L.
關鍵字: fucoxanthin;PXR;CYP3A4;MDR1;drug resistance;rifampin;constitutive androstane receptor;orphan nuclear receptors;cancer-cells;multidrug-resistance;signaling pathway;metabolism;activation;apoptosis;induction;mice
Project: Marine Drugs
期刊/報告no:: Marine Drugs, Volume 10, Issue 1, Page(s) 242-257.
摘要: 
Pregnane X receptor (PXR) has been reported to regulate the expression of drug-metabolizing enzymes, such as the cytochrome P450 3A (CYP3A) family and transporters, such as multiple drug resistance 1 (MDR1). Fucoxanthin, the major carotenoid in brown sea algae, is a putative chemopreventive agent. In this study, we determined whether fucoxanthin could overcome drug resistance through attenuation of rifampin-induced CYP3A4 and MDR1 gene expression by PXR-mediated pathways in HepG2 hepatoma cells. We found that fucoxanthin (1-10 mu M) significantly attenuated rifampin (20 mu M)-induced CYP3A4, MDR1 mRNA and CYP3A4 protein expression at 24 h of incubation. Mechanistically, fucoxanthin strongly attenuated the PXR-mediated CYP3A4 promoter activity in HepG2 cells. In addition, fucoxanthin attenuated constitutive androstane receptor (CAR)- and rPXR-mediated CYP3A4 promoter activity in this cell line. Using the mammalian two-hybrid assay, we found that fucoxanthin significantly decreased the interaction between PXR and SRC-1, a PXR co-activator. Thus, fucoxanthin can decrease rifampin-induced CYP3A4 and MDR1 expression through attenuation of PXR-mediated CYP3A4 promoter activation and interaction between PXR and co-activator. These findings could lead to potentially important new therapeutic and dietary approaches to reduce the frequency of adverse drug reactions.
URI: http://hdl.handle.net/11455/70631
ISSN: 1660-3397
DOI: 10.3390/md10010242
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