Title : Regulation of CYP3A4 by the bile acid receptor FXR: evidence for functional binding sites in the CYP3A4 gene.

Pub. Date : 2004 Oct

PMID : 15454728






5 Functional Relationships(s)
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1 CYP3A4 expression is highly variable and is induced by numerous compounds of exogenous and endogenous origin, including elevated concentrations of secondary bile acids via the pregnane X receptor (PXR). Bile Acids and Salts nuclear receptor subfamily 1, group I, member 2 Mus musculus
2 CYP3A4 expression is highly variable and is induced by numerous compounds of exogenous and endogenous origin, including elevated concentrations of secondary bile acids via the pregnane X receptor (PXR). Bile Acids and Salts nuclear receptor subfamily 1, group I, member 2 Mus musculus
3 Thus, whereas elevated concentrations of precursors of bile acids and secondary bile acids induce CYP3A via PXR, primary bile acids can modulate the expression of CYP3A via FXR. Bile Acids and Salts nuclear receptor subfamily 1, group I, member 2 Mus musculus
4 Thus, whereas elevated concentrations of precursors of bile acids and secondary bile acids induce CYP3A via PXR, primary bile acids can modulate the expression of CYP3A via FXR. Bile Acids and Salts nuclear receptor subfamily 1, group I, member 2 Mus musculus
5 Thus, whereas elevated concentrations of precursors of bile acids and secondary bile acids induce CYP3A via PXR, primary bile acids can modulate the expression of CYP3A via FXR. Bile Acids and Salts nuclear receptor subfamily 1, group I, member 2 Mus musculus