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Inhibition of Breast Cancer Resistance Protein and Multidrug Resistance Associated Protein 2 by Natural Compounds and Their Derivatives

Abcg2型 多药耐药蛋白2 药理学 化学 ATP结合盒运输机 多重耐药 ABCC1公司 多药耐药相关蛋白 生物利用度 IC50型 运输机 生物化学 生物 体外 基因 抗生素
作者
Noora Sjöstedt,Kira Holvikari,Päivi Tammela,Heidi Kidron
出处
期刊:Molecular Pharmaceutics [American Chemical Society]
卷期号:14 (1): 135-146 被引量:42
标识
DOI:10.1021/acs.molpharmaceut.6b00754
摘要

The food and dietary supplements we consume contain a wide variety of plant secondary metabolites and other compounds, which, like drugs, can be absorbed, metabolized, distributed, and excreted from the body. In the intestine, these compounds can interact with transport proteins such as the multidrug resistance associated protein 2 (MRP2, ABCC2) and the breast cancer resistance protein (BCRP, ABCG2) that regulate the absorption of drugs and other compounds. Inhibition of these transporters by dietary components could lead to increased exposure and adverse effects of concomitantly administered drugs. Therefore, we screened a library of 124 natural compounds and their derivatives using the vesicular transport assay to evaluate their inhibitory potential on MRP2 and BCRP. Of the library compounds, 36% were identified as BCRP inhibitors, whereas the number was only 3.2% for MRP2. BCRP inhibitors are described by higher molecular weight, number of rings, aromaticity, and LogD7.4 than noninhibitors. IC50 values were measured for six dual inhibitors, among which three novel inhibitors, gossypin, nordihydroguaiaretic acid, and octyl gallate, were identified. Our results confirm that flavonoids are avid inhibitors of BCRP, and flavones and flavonols appear to be important subclasses of flavonoids for this inhibition. The strong inhibition of BCRP transport by some compounds suggests that their presence at high levels in the diet could cause food–drug interactions, but this seems to be a minor cause of concern for MRP2.
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