Bile acid metabolism and signalling in liver disease.

J Hepatol

Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria. Electronic address:

Published: January 2025

AI Article Synopsis

  • * Disruptions in BA functions can lead to various liver diseases, including cholestatic disorders and conditions like metabolic dysfunction-associated steatotic liver disease (MASLD), as well as increase risks for certain cancers.
  • * The review aims to discuss the latest findings on BA signaling, metabolism, and transport, highlighting new therapeutic approaches targeting BAs for treating liver and metabolic diseases.

Article Abstract

Bile acids (BAs) serve as signalling molecules, efficiently regulating their own metabolism and transport, as well as key aspects of lipid and glucose homeostasis. BAs shape the gut microbial flora and conversely are metabolised by microbiota. Disruption of BA transport, metabolism and physiological signalling functions contribute to the pathogenesis and progression of a wide range of liver diseases including cholestatic disorders and MASLD (metabolic dysfunction-associated steatotic liver disease), as well as hepatocellular and cholangiocellular carcinoma. Additionally, impaired BA signalling may also affect the intestine and kidney, thereby contributing to failure of gut integrity and driving the progression and complications of portal hypertension, cholemic nephropathy and the development of extrahepatic malignancies such as colorectal cancer. In this review, we will summarise recent advances in the understanding of BA signalling, metabolism and transport, focusing on transcriptional regulation and novel BA-focused therapeutic strategies for cholestatic and metabolic liver diseases.

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Source
http://dx.doi.org/10.1016/j.jhep.2024.09.032DOI Listing

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