Molecular mechanisms of transporter regulation and their impairment in intrahepatic cholestasis

Author:

Li Xiping1,Zu Yue1,Li Guodong1,Xiang Dong1,Zhang Chengliang1,Liu Dong1

Affiliation:

1. Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China

Abstract

Intrahepatic cholestasis (IC) is a liver disease caused by disorders in bile formation and excretion, owing to structural and functional abnormalities in hepatocytes and/or bile capillaries. IC is commonly caused by hepatitis virus, alcohol consumption, drug-induced liver damage, autoimmune liver disease and heredity. In the absence of effective treatment, IC can progress to liver fibrosis, cirrhosis and ultimately liver failure. However, the mechanisms underlying IC remain poorly understood. IC is believed to be closely associated with changes in the transcription, function and localization of hepatocellular transport proteins. To better understand the molecular mechanisms of transport proteins in IC, herein, we review the roles of these transport proteins and discuss their underlying regulatory mechanisms in IC. Our aim is to provide a reference for understanding IC pathogenesis and developing effective drug therapies.

Publisher

Compuscript, Ltd.

Reference105 articles.

1. Molecular Overview of Progressive Familial Intrahepatic Cholestasis;S Amirneni;World Journal of Gastroenterology,2020

2. Molecular Pathogenesis of Intrahepatic Cholestasis of Pregnancy;J Xiao;Canadian Journal of Gastroenterology and Hepatology,2021

3. Molecular Pathogenesis of Cholestasis;M Trauner;The New England Journal of Medicine,1998

4. Hepatocellular Transporters and Cholestasis;C Pauli-Magnus;Journal of Clinical Gastroenterology,2005

5. The Pathological Mechanisms of Estrogen-Induced Cholestasis: Current perspectives;Y Zu;Frontiers in Pharmacology,2021

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