Diallyl disulfide, a chemopreventive agent in garlic, induces multidrug resistance-associated protein 2 expression

被引:37
作者
Demeule, M [1 ]
Brossard, M [1 ]
Turcotte, S [1 ]
Regina, A [1 ]
Jodoin, J [1 ]
Béliveau, R [1 ]
机构
[1] Univ Quebec, Hop St Justine, Mol Med Lab, Montreal, PQ H3C 3P8, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
P-glycoprotein; canalicular multispecific organic anion transporter; Mrp2; diallyl disulfide; S-Allyl cysteine; cisplatin;
D O I
10.1016/j.bbrc.2004.09.141
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The organosulfur compounds (OSCs), present in garlic, are studied for their protective effect against human cancers. P-glycoprotein (P-gp) and multidrug resistance protein 2 (Mrp2) are two transporters involved in the defense of cells and in the development of multidrug resistance. Whereas OSCs increase glutathione S-transferase activity (GST), Mrp2 plays a role in the transport of glutathione (GSH)-conjugates. In this study, we have investigated the effect of two OSCs, diallyl disulfide (DADS) and S-allyl cysteine (SAC), on P-gp and Mrp2 expression in renal brush-border membranes. By Western blot analysis, our results show that DADS induces Mrp2-expression (by 7-fold), which correlates with the rise of GST activity and GSH levels. Surprisingly, a co-administration of OSC with cisplatin, an anticancer drug, significantly increased Mrp2 gene and protein expression (by 30-fold), suggesting that DADS could potentiate the effects of cisplatin. Interestingly, SAC and cisplatin in co-treatment decreased P-gp protein expression and mdr1b isoform mRNA levels. In addition, modulation of the mdr1b isoform and Mrp2 by cisplatin was completely abolished by a glutathione precursor, N-acetyl cysteine. These results indicate that OSCs present in a garlic-rich diet might alter chemotherapeutic treatments using P-gp or Mrp2 substrates. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:937 / 945
页数:9
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