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

被引:18
作者
Beumer, Jan-Hendrik
Buckle, Tessa
Ouwehand, Mariet
Franke, Niels E. F.
Lopez-Lazaro, Luis
Schellens, Jan H. M.
Beijnen, Jos H.
van Tellingen, Olaf
机构
[1] Netherlands Canc Inst, NL-1066 CX Amsterdam, Netherlands
[2] Slotervaart Hosp, Dept Pharm & Pharmacol, Netherlands Canc Inst, Amsterdam, Netherlands
[3] Antoni Van Leeuwenhoek Hosp, Netherlands Canc Inst, Dept Clin Chem, Amsterdam, Netherlands
[4] PharmaMar, Clin Pharmacol, Madrid, Spain
[5] Antoni Van Leeuwenhoek Hosp, Netherlands Canc Inst, Dept Med Oncol, Amsterdam, Netherlands
[6] Univ Utrecht, Dept Biomed Anal, Div Drug Toxicol, Fac Pharmaceut Sci, Utrecht, Netherlands
关键词
D O I
10.1007/s10637-006-7773-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Trabectedin (ET-743, Yondelis (TM)) 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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页码:1 / 7
页数:7
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