Inhibition of drug transport by genistein in multidrug-resistant cells expressing P-glycoprotein

被引:136
作者
Castro, AF [1 ]
Altenberg, GA [1 ]
机构
[1] UNIV TEXAS,MED BRANCH,DEPT PHYSIOL & BIOPHYS,GALVESTON,TX 77555
关键词
multidrug resistance; drug transport; photoaffinity labeling; MRP; tyrosine kinase; phosphorylation;
D O I
10.1016/S0006-2952(96)00657-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
It has been claimed that the flavonoid genistein could be used to distinguish multidrug-resistant tumors expressing the multidrug resistance-associated protein (MRP) from those expressing P-glycoprotein (Pgp). Genistein would block drug transport by MRP without affecting Pgp-mediated drug transport. However, we found that exposure to 200 mu M genistein elicited an elevation in intracellular accumulation of rhodamine 123 (R123) and daunorubicin (DNR) in Pgp-expressing cell lines. Genistein inhibited R123 efflux in a rapidly reversible manner (ca. 2 min). The flavonoid also decreased photoaffinity labeling of Pgp by [H-3]azidopine, a Pgp substrate. The present results show that genistein interacts with Pgp and inhibits Pgp-mediated drug transport. Hence, genistein cannot be used in simple assays to distinguish MRP- and Pgp-expressing cells. Copyright (C) 1996 Elsevier Science Inc.
引用
收藏
页码:89 / 93
页数:5
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