EXPRESSION OF P-GLYCOPROTEIN IN EPITHELIAL OVARIAN-CANCER - EVALUATION AS A MARKER OF MULTIDRUG RESISTANCE

被引:38
作者
RUBIN, SC [1 ]
FINSTAD, CL [1 ]
HOSKINS, WJ [1 ]
SAIGO, PE [1 ]
PROVENCHER, DM [1 ]
FEDERICI, MG [1 ]
HAKES, TB [1 ]
MARKMAN, M [1 ]
REICHMAN, BS [1 ]
LLOYD, KO [1 ]
LEWIS, JL [1 ]
机构
[1] MEM SLOAN KETTERING CANC CTR,NEW YORK,NY 10021
关键词
chemotherapy; multidrug resistance; ovarian cancer; P-Glycoprotein;
D O I
10.1016/S0002-9378(11)90670-X
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The multidrug-resistance gene, MDR1, encodes a plasma membrane glycoprotein termed P-glycoprotein that mediates active cellular efflux of certain chemotherapeutic agents. P-Glycoprotein expression was evaluated in 98 frozen tumor specimens from 57 patients with epithelial ovarian cancer by the indirect immunoperoxidase technique with monoclonal antibodies C219 and JSB-1 used for detection. Tumor specimens were further characterized antigenically with a panel of monoclonal antibodies representing a variety of epithelial cell antigens. Included were 57 specimens from 33 previously untreated patients; 11 specimens were also available from eight patients in this group after chemotherapy. An additional 30 specimens were studied from 24 other patients after chemotherapy. In only four of the 57 patients with ovarian cancer (7%) did one or more of the specimens express P-glycoprotein. Two of these patients had tumors that were considered clinically drug resistant. No increase in P-glycoprotein expression was noted after exposure to chemotherapy, including the eight individuals for whom specimens were available both before and after treatment. Although drug resistance is a major problem in treatment of ovarian cancer, resistance to the drugs most active against these tumors probably occurs through a mechanism other than expression of the MDR1 gene product. © 1990, Mosby. All rights reserved.
引用
收藏
页码:69 / 73
页数:5
相关论文
共 16 条
[1]   DETECTION OF P-GLYCOPROTEIN IN OVARIAN-CANCER - A MOLECULAR MARKER ASSOCIATED WITH MULTIDRUG RESISTANCE [J].
BELL, DR ;
GERLACH, JH ;
KARTNER, N ;
BUICK, RN ;
LING, V .
JOURNAL OF CLINICAL ONCOLOGY, 1985, 3 (03) :311-315
[2]  
BERRY JM, 1989, P AM ASS CANCER RES
[3]  
BOURHIS J, 1989, CANCER RES, V49, P5062
[4]  
CHAN HSL, 1988, LAB INVEST, V59, P870
[5]   DRUG-RESISTANCE IN MULTIPLE-MYELOMA AND NON-HODGKINS LYMPHOMA - DETECTION OF P-GLYCOPROTEIN AND POTENTIAL CIRCUMVENTION BY ADDITION OF VERAPAMIL TO CHEMOTHERAPY [J].
DALTON, WS ;
GROGAN, TM ;
MELTZER, PS ;
SCHEPER, RJ ;
DURIE, BGM ;
TAYLOR, CW ;
MILLER, TP ;
SALMON, SE .
JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (04) :415-424
[6]   TOREMIFENE - PHARMACOLOGIC AND PHARMACOKINETIC BASIS OF REVERSING MULTIDRUG RESISTANCE [J].
DEGREGORIO, MW ;
FORD, JM ;
BENZ, CC ;
WIEBE, VJ .
JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (09) :1359-1364
[7]  
INABA M, 1984, JPN J CANCER RES, V75, P1049
[8]   DETECTION OF P-GLYCOPROTEIN IN MULTIDRUG-RESISTANT CELL-LINES BY MONOCLONAL-ANTIBODIES [J].
KARTNER, N ;
EVERNDENPORELLE, D ;
BRADLEY, G ;
LING, V .
NATURE, 1985, 316 (6031) :820-823
[9]   VERAPAMIL AND ADRIAMYCIN IN THE TREATMENT OF DRUG-RESISTANT OVARIAN-CANCER PATIENTS [J].
OZOLS, RF ;
CUNNION, RE ;
KLECKER, RW ;
HAMILTON, TC ;
OSTCHEGA, Y ;
PARRILLO, JE ;
YOUNG, RC .
JOURNAL OF CLINICAL ONCOLOGY, 1987, 5 (04) :641-647
[10]  
RAMU A, 1984, CANCER RES, V44, P144