Ovarian cancer cells cisplatin sensitization agents selected by mass cytometry target ABCC2 inhibition

Author:

Comsa Elisabeta12,Nguyen Kim-Anh34,Loghin Felicia2,Boumendjel Ahcène34,Peuchmaur Marine34,Andrieu Thibault5,Falson Pierre1

Affiliation:

1. Drug Resistance & Membrane Proteins Laboratory, Molecular Microbiology & Structural Biochemistry, UMR 5086 CNRS/Université Lyon 1, Institut de Biologie et Chimie des Protéines, Lyon, France

2. Toxicology Department, Faculty of Pharmacy, University of Medicine & Pharmacy ‘Iuliu Hatieganu’, Cluj-Napoca, Romania

3. Département de Pharmacochimie Moléculaire DPM, Univ. Grenoble Alpes, UMR 5063, 38041 Grenoble, France

4. CNRS, DPM UMR 5063, 38041 Grenoble, France

5. SFR Biosciences, Tour 1, UMS 3444 Lyon, France

Abstract

Aim: Cisplatin resistance in ovarian cancer remains a complex problem as tumors frequently develop resistance against drugs, a mechanism sometimes mediated by ATP-Binding Cassette transporters. Our goal was to find compounds restricting their inhibition capacity to the cisplatin efflux mediated by ABCC2 pump, among previously identified inhibitors, derived from the 2- indolylmethylenebenzofuranones. Methodology & results: An original method setup allows direct quantitation of platinum by employing cyTOF mass cytometry. Among tested derivatives, some led to a full platinum accumulation and efficiently resensitized cisplatin-resistant A2780 cells to cisplatin while preserving most of the calcein efflux activity. Conclusion: CyTOF is therefore a powerful and promising method to quantify cisplatin accumulation that may be used in the clinical setting to improve and personalize cancer treatment.

Publisher

Future Science Ltd

Subject

Drug Discovery,Pharmacology,Molecular Medicine

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