ROLE OF P-GLYCOPROTEIN IN DOLASTATIN-10 RESISTANCE

被引:30
作者
TOPPMEYER, DL [1 ]
SLAPAK, CA [1 ]
CROOP, J [1 ]
KUFE, DW [1 ]
机构
[1] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,DIV PEDIAT ONCOL,BOSTON,MA 02115
关键词
DOLASTATIN; 10; MULTIDRUG RESISTANCE; P-GLYCOPROTEIN; CYTOTOXIC PEPTIDES; PEPTIDE TRANSPORT; TUBULIN BINDING DRUG;
D O I
10.1016/0006-2952(94)90292-5
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dolastatin 10, a cytotoxic pentapeptide isolated from the mollusk Dolabella auricularia, exhibits potent antitumor activity. The present studies demonstrated that sublines of murine PC4 and human U-937 leukemia cells expressing a multidrug resistance (MDR) phenotype are cross-resistant to this agent. We also demonstrated that such resistance was reversed by verapamil. While these findings suggested the involvement of the P-glycoprotein (P-gp) in dolastatin 10 resistance, we performed similar studies in a CHO cell line transfected with the human mdr1 cDNA. Expression of P-gp in the transfected cells was associated with resistance to dolastatin 10 by a verapamil-sensitive mechanism. The demonstration that photoaffinity labeling of P-gp was decreased in the presence of dolastatin 10 further supports the interaction of this cytotoxic peptide with P-gp. Taken together, these findings suggest that resistance to dolastatin 10 is conferred, at least in part, by P-gp and that this cytotoxic peptide is a novel member of the MDR phenotype
引用
收藏
页码:609 / 612
页数:4
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