Fuchs Claudia D, Simbrunner Benedikt, Baumgartner Maximillian, Campbell Clarissa, Reiberger Thomas, Trauner Michael
Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria.
Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria; CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
J Hepatol. 2025 Jan;82(1):134-153. doi: 10.1016/j.jhep.2024.09.032. Epub 2024 Sep 28.
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.
胆汁酸(BAs)作为信号分子,有效调节自身的代谢和转运,以及脂质和葡萄糖稳态的关键方面。胆汁酸塑造肠道微生物群,反之,微生物群也会对其进行代谢。胆汁酸转运、代谢和生理信号功能的破坏会导致包括胆汁淤积性疾病和代谢功能障碍相关脂肪性肝病(MASLD)以及肝细胞癌和胆管细胞癌在内的多种肝脏疾病的发病机制和进展。此外,胆汁酸信号受损也可能影响肠道和肾脏,从而导致肠道完整性受损,并推动门静脉高压、胆血症肾病的进展和并发症以及结直肠癌等肝外恶性肿瘤的发生。在本综述中,我们将总结对胆汁酸信号、代谢和转运的最新认识进展,重点关注转录调控以及针对胆汁淤积性和代谢性肝病的新型胆汁酸靶向治疗策略。