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新型普伐他汀摄取转运体有机阴离子转运体7/SLC22A9肝脏表达的变异性:遗传和调节因素的影响

Variability in hepatic expression of organic anion transporter 7/SLC22A9, a novel pravastatin uptake transporter: impact of genetic and regulatory factors.

作者信息

Emami Riedmaier A, Burk O, van Eijck B A C, Schaeffeler E, Klein K, Fehr S, Biskup S, Müller S, Winter S, Zanger U M, Schwab M, Nies A T

机构信息

Dr. Margarete Fischer-Bosch Institute of Clinical Pharmacology, Stuttgart, Germany.

University of Tübingen, Tübingen, Germany.

出版信息

Pharmacogenomics J. 2016 Aug;16(4):341-51. doi: 10.1038/tpj.2015.55. Epub 2015 Aug 4.

Abstract

Human organic anion transporter 7 (OAT7, SLC22A9) is a hepatic transport protein poorly characterized so far. We therefore sought to identify novel OAT7 substrates and factors contributing to variable hepatic OAT7 expression. Using OAT7-expressing cells, pravastatin was identified as a substrate. Hepatic SLC22A9/OAT7 mRNA and protein expression varied 28-fold and 15-fold, respectively, in 126 Caucasian liver samples. Twenty-four variants in SLC22A9 were genotyped, including three rare missense variants (rs377211288, rs61742518, rs146027075), which occurred only heterozygously. No variant significantly affected hepatic SLC22A9/OAT7 expression. The three missense variants, however, showed functional consequences when expressed in vitro. Hepatic nuclear factor 4-alpha (HNF4α) emerged as a major transcriptional regulator of SLC22A9 by a series of in silico and in vitro analyses. In conclusion, pravastatin is the first identified OAT7 drug substrate. Substantial inter-individual variability in hepatic OAT7 expression, majorly driven by HNF4α, may contribute to pravastatin drug disposition and might affect response.The Pharmacogenomics Journal advance online publication, 4 August 2015; doi:10.1038/tpj.2015.55.

摘要

人类有机阴离子转运体7(OAT7,SLC22A9)是一种目前特征尚不明确的肝脏转运蛋白。因此,我们试图鉴定OAT7的新底物以及导致肝脏OAT7表达存在差异的因素。利用表达OAT7的细胞,普伐他汀被鉴定为一种底物。在126份白种人肝脏样本中,肝脏SLC22A9/OAT7 mRNA和蛋白表达分别有28倍和15倍的差异。对SLC22A9中的24个变异进行了基因分型,包括3个罕见的错义变异(rs377211288、rs61742518、rs146027075),这些变异仅以杂合子形式出现。没有变异对肝脏SLC22A9/OAT7表达有显著影响。然而,这3个错义变异在体外表达时显示出功能后果。通过一系列计算机模拟和体外分析,肝细胞核因子4α(HNF4α)成为SLC22A9的主要转录调节因子。总之,普伐他汀是首个被鉴定的OAT7药物底物。肝脏OAT7表达存在显著的个体间差异,主要由HNF4α驱动,这可能影响普伐他汀的药物处置并可能影响反应。《药物基因组学杂志》在线优先发表,2015年8月4日;doi:10.1038/tpj.2015.55

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