Lower expression of HNF4α and PGC1α might impair rifampicin-mediated CYP3A4 induction under conditions where PXR is overexpressed in human fetal liver cells.
@article{Takezawa2012LowerEO, title={Lower expression of HNF4$\alpha$ and PGC1$\alpha$ might impair rifampicin-mediated CYP3A4 induction under conditions where PXR is overexpressed in human fetal liver cells.}, author={Takashi Takezawa and Tamihide Matsunaga and Kaori Aikawa and Katsunori Nakamura and Shigeru Ohmori}, journal={Drug metabolism and pharmacokinetics}, year={2012}, volume={27 4}, pages={ 430-8 } }
Pregnane X receptor (PXR) mRNA was detected in HepG2 cells by RT-PCR, but not in human fetal liver (HFL) cells. CYP3A4 was induced by rifampicin (RIF), mifepristone (RU486), clotrimazole (CTZ), and dexamethasone (DEX) in HepG2 cells, while these PXR ligands with the exception of DEX did not induce CYP3A4 mRNA expression in HFL cells. Ad-PXR infection increased mRNA levels of PXR and CYP3A4 in both cells despite the absence of PXR ligands. Similar results were observed in reporter gene assays…
14 Citations
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References
SHOWING 1-10 OF 59 REFERENCES
Underexpressed Coactivators PGC1α AND SRC1 Impair Hepatocyte Nuclear Factor 4α Function and Promote Dedifferentiation in Human Hepatoma Cells*
- Biology, MedicineJournal of Biological Chemistry
- 2006
The results suggest that SRC1, and notably PGC1α, are key coactivators for the proper function of HNF4α in human liver and for an integrative control of multiple hepatic genes involved in metabolism and homeostasis.
Comparison of basal gene expression and induction of CYP3As in HepG2 and human fetal liver cells.
- Biology, MedicineBiological & pharmaceutical bulletin
- 2007
The character of HFL cells with regard to CYP expression was different from that of HepG2 cells, and CYP3A5 mRNA expression levels were markedly up-regulated by dexamethasone (DEX), but not by rifampicin (RIF).
Evaluation of induction of CYP3A mRNA using the HepG2 cell line and reverse transcription-PCR.
- Biology, MedicineBiological & pharmaceutical bulletin
- 1999
C cultured HepG2 cells constitutively expressed CYP3A mRNA, which was expressed at high levels in culture for several days and was further induced by several drugs (e.g. rifampicin (RFP), dexamethasone) using semi-quantitative reverse transcription-PCR.
Induction of CYP3As in HepG2 cells by several drugs. Association between induction of CYP3A4 and expression of glucocorticoid receptor.
- Biology, MedicineBiological & pharmaceutical bulletin
- 2003
The regulation of CYP3A4 gene expression was hGRalpha-dependent and that ciclosporin may function as a regulator of expression via h GRalpha, which suggested that each cluster might be associated with different mechanism(s) of induction by these drugs.
Underexpressed coactivators PGC1alpha and SRC1 impair hepatocyte nuclear factor 4 alpha function and promote dedifferentiation in human hepatoma cells.
- Biology, MedicineThe Journal of biological chemistry
- 2006
The results suggest that SRC1, and notably PGC1alpha, are key coactivators for the proper function of HNF4alpha in human liver and for an integrative control of multiple hepatic genes involved in metabolism and homeostasis.
RIFAMPICIN INDUCTION OF CYP3A4 REQUIRES PREGNANE X RECEPTOR CROSS TALK WITH HEPATOCYTE NUCLEAR FACTOR 4α AND COACTIVATORS, AND SUPPRESSION OF SMALL HETERODIMER PARTNER GENE EXPRESSION
- Biology, MedicineDrug Metabolism and Disposition
- 2006
Results suggest that PXR strongly induces CYP3A4 gene transcription by interacting with HNF4α, SRC-1, and PGC-1α, and concomitantly inhibits SHP gene transcription and maximizes the P XR induction of the CYP 3A 4 gene in human livers.
Expression and induction of CYP3As in human fetal hepatocytes.
- Biology, MedicineBiochemical and biophysical research communications
- 2004
The orphan nuclear receptor HNF4α determines PXR- and CAR-mediated xenobiotic induction of CYP3A4
- Biology, MedicineNature Medicine
- 2003
It is shown that the orphan nuclear receptor hepatocyte nuclear factor-4α (HNF4α; HNF4A) is critically involved in the PXR- and CAR-mediated transcriptional activation of CYP3A4, an important regulator of coordinate nuclear-receptor–mediated response to xenobiotics.
Quantitative analysis of constitutive and inducible CYPs mRNA expression in the HepG2 cell line using reverse transcription-competitive PCR.
- Biology, MedicineBiochemical and biophysical research communications
- 2000
This study demonstrates the efficiency of a combination of HepG2 cells and RT-cPCR in the evaluation of CYP3A mRNA-induction by drugs and reports for the first time quantitative profiles of CYPs mRNA in HepG1 cells.
In vivo activation of the human CYP3A4 promoter in mouse liver and regulation by pregnane X receptors.
- Biology, MedicineBiochemical pharmacology
- 2003