Planta Med 2006; 72(12): 1121-1126
DOI: 10.1055/s-2006-941546
Original Paper
Pharmacology
© Georg Thieme Verlag KG Stuttgart · New York

Reduction of Cytotoxicity of the Alkaloid Emetine through P-Glycoprotein (MDR1/ABCB1) in Human Caco-2 Cells and Leukemia Cell Lines

Maren Möller1 , Johanna Weiss2 , Michael Wink1
  • 1Institute of Pharmacy and Molecular Biotechnology, University of Heidelberg, Heidelberg, Germany
  • 2Department of Internal Medicine VI, Clinical Pharmacology and Pharmacoepidemiology, University of Heidelberg, Heidelberg, Germany
In memory of Professor Ernst Reinhard
Further Information

Publication History

Received: February 10, 2006

Accepted: April 27, 2006

Publication Date:
19 June 2006 (online)

Abstract

The cytotoxicity of the alkaloid emetine was determined in six human cell lines that differ in the expression of ABC transporters, such as multiple drug resistance protein 1 (MDR1/ABCB1) and multidrug resistance associated protein 1 (MRP1/ABCC1). Emetine reveals a substantial cytotoxicity due to apoptosis that is inversely correlated with the expression of MDR1. Confluent Caco-2 cells with high MDR1 activity and the MDR1 over-expressing leukemia cell line CEM/ADR5000 are more resistant towards emetine (EC50 250 μM and 2 μM, respectively) than cells with a low expression of MDR1 (Jurkat cells, CCRF-CEM cells, HL-60 cells) or cells which over-express MRP1 (HL-60/AR) (EC50 between 0.05 μM for CCRF-CEM and 0.17 μM for Jurkat cells). Apparently emetine is a substrate for MDR1 but not for MRP1. Furthermore, emetine is able to up-regulate the expression of MDR1 as shown in vitro by real-time PCR and transport activity studies.

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Prof. Dr. Michael Wink

Institute of Pharmacy and Molecular Biotechnology

Department of Biology

University of Heidelberg

Im Neuenheimer Feld 364

69120 Heidelberg

Germany

Phone: +49-6221-54-4880

Fax: +49-6221-54-4884

Email: wink@uni-hd.de

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