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Hepatic bile acid metabolism genes

Molecular classification
Enzyme, Receptor, Transporter, Transcription factor
01

Overview

The term "Hepatic bile acid metabolism genes" refers to a collective group of proteins rather than a single therapeutic target. This network includes enzymes like Cholesterol 7-alpha-hydroxylase (CYP7A1), transporters such as the Bile Salt Export Pump (BSEP), and nuclear receptors like the Farnesoid X receptor (FXR) (Chiang, 2013, PMID: 23720281). These genes work in concert to regulate the synthesis of bile acids from cholesterol and their circulation between the liver and intestine, a process vital for lipid absorption and metabolic signaling (UniProt P22680). Dysregulation within this pathway is a key driver of cholestatic diseases and metabolic disorders like nonalcoholic steatohepatitis (NASH) (Trauner et al., 2017, PMID: 28838987). While the group as a whole is not a single target, individual components are targeted by drugs such as obeticholic acid (FXR agonist) and odevixibat (ASBT inhibitor) to manage bile acid levels and associated symptoms like pruritus (FDA, 2016; FDA, 2021).

Other names
Bile acid synthesis pathwayEnterohepatic circulation genesHepatic bile acid signaling network
02

Mechanism of action

Modulation of bile acid synthesis, transport, and signaling via nuclear receptor activation or transporter inhibition.

03

Biological functions

Lipid metabolismCholesterol homeostasisSignal transductionBile acid synthesis
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Disease associations

CholestasisNonalcoholic steatohepatitis (NASH)Primary biliary cholangitis (PBC)Primary sclerosing cholangitis (PSC)Gallstones
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Safety considerations

PruritusDiarrheaHepatotoxicity riskIncreased LDL cholesterol
06

Interacting drugs

Obeticholic acid

5 more in the full profile.

07

Biomarkers

7α-hydroxy-4-cholesten-3-one (C4)Fibroblast growth factor 19 (FGF19)Total serum bile acids

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