ABCG2对肠上皮屏障通透性的表达、功能及调控

IF 2.1 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ping Shi, Lianhua Tang, Fei Yin, Hong Guo, Jianhui Liu
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引用次数: 0

摘要

人乳腺癌耐药蛋白(BCRP,基因符号ABCG2)是一种atp结合盒(ABC)外排转运蛋白,高表达于肠上皮顶端膜,参与外源物的吸收、分布、消除和内源性分子的外排。此外,肠上皮单层是内环境与体循环之间最大的界面和最重要的功能屏障。大量研究表明,人类和啮齿类动物的肠道ABCG2通过调节肠道上皮屏障的分布,在限制外源药物在小肠中的吸收方面起着至关重要的作用。因此,肠上皮屏障中ABCG2的表达、功能和活性的变化在药物反应和副作用中起着重要作用。本文就ABCG2在肠道药物转运、肠道尿酸排泄、肠道屏障功能障碍等方面的研究进展,以及其在人类肠道疾病中改变肠上皮屏障通透性的作用进行综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression, Function, and Regulation of ABCG2 on the Intestinal Epithelial Barrier Permeability.

Human breast cancer resistance protein (BCRP, gene symbol ABCG2) is an ATP-binding cassette (ABC) efflux transporter that is highly expressed on the apical membranes of intestinal epithelium and contributes to the absorption, distribution, and elimination of xenobiotics and the efflux of endogenous molecules. Also, the intestinal epithelial monolayer is the largest interface and the most important functional barrier between the internal environment and the systemic circulation. Extensive studies have demonstrated that intestinal ABCG2 of humans and rodents plays a crucial role in limiting absorption of xenobiotics, which are ABCG2 transport substrates, in the small intestine by mediating distribution in the intestinal epithelial barrier. Therefore, changes in the expression, function and activity of ABCG2 in the intestinal epithelial barrier play important roles in drug response and side effects. In this review, we specifically summarize the current research progress of ABCG2 in intestinal drug transport, intestinal urate excretion and intestinal barrier dysfunction, and its role in altering the intestinal epithelial barrier permeability in human intestinal disorder.

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来源期刊
Current drug metabolism
Current drug metabolism 医学-生化与分子生物学
CiteScore
4.30
自引率
4.30%
发文量
81
审稿时长
4-8 weeks
期刊介绍: Current Drug Metabolism aims to cover all the latest and outstanding developments in drug metabolism, pharmacokinetics, and drug disposition. The journal serves as an international forum for the publication of full-length/mini review, research articles and guest edited issues in drug metabolism. Current Drug Metabolism is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the most important developments. The journal covers the following general topic areas: pharmaceutics, pharmacokinetics, toxicology, and most importantly drug metabolism. More specifically, in vitro and in vivo drug metabolism of phase I and phase II enzymes or metabolic pathways; drug-drug interactions and enzyme kinetics; pharmacokinetics, pharmacokinetic-pharmacodynamic modeling, and toxicokinetics; interspecies differences in metabolism or pharmacokinetics, species scaling and extrapolations; drug transporters; target organ toxicity and interindividual variability in drug exposure-response; extrahepatic metabolism; bioactivation, reactive metabolites, and developments for the identification of drug metabolites. Preclinical and clinical reviews describing the drug metabolism and pharmacokinetics of marketed drugs or drug classes.
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