ABCG2: recent discovery of potent and highly selective inhibitors

Author:

Lecerf-Schmidt Florine1,Peres Basile1,Valdameri Glaucio23,Gauthier Charlotte2,Winter Evelyn2,Payen Léa456,Di Pietro Attilio2,Boumendjel Ahcène7

Affiliation:

1. Université Joseph Fourier, Grenoble 1, CNRS UMR 5063, Département de Pharmacochimie Moléculaire, Grenoble, France

2. Equipe Labellisée Ligue 2013, BMSSI UMR 5086 CNRS/Université Lyon 1, IBCP, Lyon, France

3. Department of Biochemistry & Molecular Biology, Federal University of Parana, Curitiba, PR, Brazil

4. Université de Lyon, Lyon 1, ISPB, Lyon, France

5. INSERM U1052, Centre de Recherche en Cancérologie de Lyon, F-69000 & Centre Léon Bérard, FNCLCC, Lyon, France

6. Hospices Civils of Lyon, Biochemistry laboratory of Lyon Sud (CBS), Lyon, France

7. Université Joseph Fourier, Grenoble 1, CNRS UMR 5063, Département de Pharmacochimie Moléculaire, Grenoble, France.

Abstract

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.

Publisher

Future Science Ltd

Subject

Drug Discovery,Pharmacology,Molecular Medicine

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