Trabectedin (ET-743, Yondelis™) is a substrate for P-glycoprotein, but only high expression of P-glycoprotein confers the multidrug resistance phenotype

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作者
Jan-Hendrik Beumer
Tessa Buckle
Mariet Ouwehand
Niels E. F. Franke
Luis Lopez-Lazaro
Jan H. M. Schellens
Jos H. Beijnen
Olaf van Tellingen
机构
[1] The Netherlands Cancer Institute/Slotervaart Hospital,Department of Pharmacy & Pharmacology
[2] The Netherlands Cancer Institute/Antoni van Leeuwenhoek Hospital,Department of Clinical Chemistry
[3] Colmenar Viejo,PharmaMar, Clinical Pharmacology
[4] The Netherlands Cancer Institute/Antoni van Leeuwenhoek Hospital,Department of Medical Oncology
[5] Utrecht University,Department of Biomedical Analysis, Division of Drug Toxicology, Faculty of Pharmaceutical Sciences
[6] Netherlands Cancer Institute,undefined
来源
Investigational New Drugs | 2007年 / 25卷
关键词
Paclitaxel; Trabectedin; Inhibitor LY335979; Mdr1 mRNA; Vectorial Transport;
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摘要
Trabectedin (ET-743, Yondelis™) is a novel anticancer drug currently undergoing phase II and III investigations. There are various and conflicting reports whether trabectedin is a substrate for P-glycoprotein (P-gp), an important factor in drug disposition and multi-drug resistance (MDR). We have now unambiguously shown that trabectedin is a P-gp substrate by investigating vectorial transport over monolayers of LLC-PK1 pig kidney and Madine-Darby Canine kidney (MDCK) cells and the mdr1a and/or MDR1 transfected subclones. We further characterized the cytotoxic effects and cellular accumulation of trabectedin in these cell lines as well as in a panel of other cell lines with high or moderate expression levels of P-gp. Trabectedin displayed the typical MDR phenotype only in highly P-gp expressing cell lines, but not in cell lines with expression levels more closely conforming to clinical samples, suggesting that P-gp will not confer resistance to trabectedin in cancer patients.
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