Modulation of P-glycoprotein function and multidrug resistance in cancer cells by Thai plant extracts

被引:6
|
作者
Takano, M. [1 ]
Kakizoe, S. [1 ]
Kawami, M. [1 ]
Nagai, J. [1 ]
Patanasethanont, D. [2 ]
Sripanidkulchai, B. [3 ]
Yumoto, R. [1 ]
机构
[1] Hiroshima Univ, Grad Sch Biomed & Hlth Sci, Dept Pharmaceut & Therapeut, Hiroshima 7348553, Japan
[2] Khon Kaen Univ, Fac Pharmaceut Sci, Khon Kaen, Thailand
[3] Khon Kaen Univ, Ctr Res & Dev Herbal Hlth Prod, Khon Kaen, Thailand
来源
PHARMAZIE | 2014年 / 69卷 / 11期
基金
日本学术振兴会;
关键词
KAEMPFERIA-PARVIFLORA EXTRACTS; MULTIPLE-DRUG RESISTANCE; TRANSPORTERS; EFFLUX; MECHANISMS; EXPRESSION; FLAVONOIDS; LINE; CHEMOTHERAPY; PACLITAXEL;
D O I
10.1691/ph.2014.4619
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The effects of ethanol extracts from Thai plants belonging to the families of Annonaceae, Rutaceae, and Zingiberaceae on P-glycoprotein (P-gp) function and multidrug resistance were examined in paclitaxel-resistant HepG2 (PR-HepG2) cells. All the extracts tested, significantly increased the accumulation of [H-3]paclitaxel, a P-gp substrate, in the cells. Among nine extracts, Z01 and Z02, extracts from Curcuma comosa and Kaempferia marginata (Zingiberaceae family), respectively, potently increased the accumulation. In addition, Z01 and Z02 increased the accumulation of other P-gp substrates, rhodamine 123 and doxorubicin, in PR-HepG2 cells in a concentration-dependent manner. Increased accumulation of rhodamine 123 and doxorubicin by Z01 and Z02 was also confirmed by confocal laser scanning microscopy. The effect of Z01 and Z02 pretreatment on the expression of MDR1 mRNA was also examined. The expression of MDR1 mRNA was not affected by the treatment of PR-HepG2 cells with these extracts for 48 hours. Cytotoxicity of paclitaxel was examined by XTT and protein assays in the absence and presence of Z02. Z02 potentiated the cytotoxicity of paclitaxel in PR-HepG2 cells. These results suggest that Curcuma comosa and Kaempferia marginata belonging to Zingiberaceae are useful sources to search for new P-gp modulator(s) that can be used to overcome multidrug resistance of cancer cells.
引用
收藏
页码:823 / 828
页数:6
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