Expression of multidrug resistance protein gene in patients with glioma after chemotherapy

被引:73
作者
Abe, T [1 ]
Mori, T
Wakabayashi, Y
Nakagawa, M
Cole, SPC
Koike, K
Kuwano, M
Hori, S
机构
[1] Oita Med Univ, Dept Neurosurg, Oita 8795593, Japan
[2] Queens Univ, Canc Res Labs, Kingston, ON, Canada
[3] Kyushu Univ, Sch Med, Dept Biochem, Fukuoka 812, Japan
关键词
glioma; MRP; MDR;
D O I
10.1023/A:1005954406809
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Two different ATP-binding membrane glycoproteins, the 170 kDa P-glycoprotein (P-gp) and the 190 kDa multidrug resistance protein (MRP), are involved in the acquisition of multidrug resistance phenotypes in cancer cells. Overexpression of P-gp is often observed in various human tumors when treated with anticancer agents. In this study, we asked whether MRP was overexpressed in human gliomas after cancer chemotherapy. We investigated expression of MRP and P-gp before and after chemotherapy in tumor samples from patients with glioma. MRP expression was observed in 16 (70%) of 23 untreated patients, and the proportion of MRP-positive cells in the whole cell population ranged from 3 to 32% in the 16 MRP-positive patients. P-gp-positive tumors were observed in 4 (18%) of 23 patients, and the proportional rates of P-gp-positive cells in the whole cell population ranged from 4 to 23%. The proportional rate of MRP-positive or P-gp-positive glioma cells increased after chemotherapy when compared with that before chemotherapy in all patients examined. We could observe no statistically significant correlation between expression of MRP or P-gp and tumor grade. These results suggest that MRP as well as P-gp may be involved in acquired or intrinsic drug resistance in human glioma.
引用
收藏
页码:11 / 18
页数:8
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