Genetic variations of bile salt transporters as predisposing factors for drug-induced cholestasis, intrahepatic cholestasis of pregnancy and therapeutic response of viral hepatitis

被引:43
作者
Stieger, Bruno [1 ,2 ]
Geier, Andreas [2 ,3 ]
机构
[1] Univ Zurich Hosp, Div Clin Pharmacol & Toxicol, CH-8091 Zurich, Switzerland
[2] Univ Zurich, Ctr Integrat Human Physiol, CH-8057 Zurich, Switzerland
[3] Univ Zurich Hosp, Div Gastroenterol & Hepatol, CH-8091 Zurich, Switzerland
基金
瑞士国家科学基金会;
关键词
acquired cholestasis; adverse drug reaction; polymorphism; viral hepatitis C; INDUCED LIVER-INJURY; EXPORT PUMP BSEP; ATP-BINDING-CASSETTE; RESISTANCE-ASSOCIATED PROTEIN-2; ENDOTHELIN ANTAGONIST BOSENTAN; PRIMARY BILIARY-CIRRHOSIS; PLURIPOTENT STEM-CELLS; ABCB4; GENE; RAT-LIVER; PROGESTERONE METABOLITES;
D O I
10.1517/17425255.2011.557067
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Areas covered: This article provides an introduction into the physiology of bile formation followed by a summary of the current knowledge on the key bile salt transporters, namely, the sodium-taurocholate co-transporting polypeptide NTCP, the organic anion transporting polypeptides (OATPs), BSEP and the multi-drug resistance protein 3. The pathophysiologic consequences of altered functions of these transporters, with an emphasis on molecular and genetic aspects, are then discussed. Expert opinion: Knowledge of the role of hepatocellullar transporters, especially BSEP, in acquired cholestasis is continuously increasing. A common variant of BSEP (p.V444A) is now a well-established susceptibility factor for acquired cholestasis and recent evidence suggests that the same variant also influences the therapeutic response and disease progression of viral hepatitis C. Studies in large independent cohorts are now needed to confirm the relevance of p.V444A. Genome-wide association studies should lead to the identification of additional genetic factors underlying cholestatic liver disease.
引用
收藏
页码:411 / 425
页数:15
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