Université Joseph Fourier, Grenoble 1, CNRS UMR 5063, Département de Pharmacochimie Moléculaire, Grenoble, France.
Future Med Chem. 2013 Jun;5(9):1037-45. doi: 10.4155/fmc.13.71.
ABCG2 impacts oral availability, tissue distribution and excretion of its substrates, including anticancer and anti-infectious drugs. Highly expressed at physiological barriers, its secretion level significantly controls drug distribution. Furthermore, its increased content into many types of cancer may lead to cell chemoresistance. Owing to the clinical relevance of ABCG2 in the multidrug resistance phenomenon, ABCG2 constitutes an appealing therapeutic target to increase drug distribution. Development of ABCG2 inhibitors can be used in combination with anticancer drugs to block the drug secretion from cancer cells. Very recently, an alternative use of ABCG2 inhibitors in enhancing the bioavailability of ABCG2 substrates has emerged. Hence, it is important to investigate ABCG2 inhibitors with high selectivity, high potency and safety. New inhibitors discovered during the last 5 years will be presented and discussed.
ABCG2 影响其底物(包括抗癌和抗感染药物)的口服生物利用度、组织分布和排泄。ABCG2 在生理屏障中高表达,其分泌水平显著控制着药物的分布。此外,其在许多类型的癌症中的含量增加可能导致细胞的化疗耐药性。由于 ABCG2 在多药耐药现象中的临床相关性,ABCG2 成为增加药物分布的有吸引力的治疗靶点。ABCG2 抑制剂的开发可以与抗癌药物联合使用,以阻止癌细胞中药物的分泌。最近,ABCG2 抑制剂在增强 ABCG2 底物的生物利用度方面的另一种用途也出现了。因此,研究具有高选择性、高效力和安全性的 ABCG2 抑制剂非常重要。本文将介绍和讨论过去 5 年中发现的新型抑制剂。