MRP and MDR1 gene expression in primary breast carcinomas

被引:0
作者
Filipits, M
Suchomel, RW
Dekan, G
Haider, K
Valdimarsson, G
Depisch, D
Pirker, R
机构
[1] UNIV VIENNA, SCH MED, DEPT ONCOL, CLIN INTERNAL MED 1, A-1090 VIENNA, AUSTRIA
[2] UNIV VIENNA, SCH MED, DEPT PATHOL, A-1090 VIENNA, AUSTRIA
[3] WIENER NEUSTADT GEN HOSP, DEPT SURG, A-2700 WIENER NEUSTADT, AUSTRIA
[4] QUEENS UNIV, CANC RES LABS, KINGSTON, ON K7L 3N6, CANADA
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中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To evaluate the clinically important mechanisms of drug resistance in breast cancer, the expression of the MRP gene and the corresponding one for the MDR1 gene were determined in primary breast carcinoma specimens by both reverse transcription-PCR (n = 134) and immunohistochemistry (n = 63), Expression of MRP RNA was observed in all breast cancer specimens, MDR1 RNA was detected in 80 (60%) of the carcinomas, Staining with monoclonal antibodies QCRL-1 and QCRL-3, which both recognize MRP, was strong in 15 (24%) and weak in the remaining 48 specimens (76%), Staining with C219, which recognizes P-glycoprotein, was strong in 6 (9%), weak in 30 (48%), and negative in 27 (43%) of the samples, Strong MRP staining was more frequent in T-3 and T-4 tumors than in T-1 and T-2 tumors and in the primary tumors of patients with distant metastases but was independent of age, menopausal status, histology, histological grade, estrogen receptor, progesterone receptor, and lymph node involvement, No correlation between MRP staining and expression of MDR1 RNA or P-glycoprotein was observed, Thus, these results indicate expression of both the MRP gene and the MDR1 gene in primary breast carcinomas and suggest that clinical drug resistance in breast cancer is most likely multifactorial.
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页码:1231 / 1237
页数:7
相关论文
共 53 条
[1]  
ABBASZADEGAN MR, 1994, CANCER RES, V54, P4676
[2]  
BAIDINI N, 1995, NEW ENGL J MED, V333, P1380
[3]   A 190-KILODALTON PROTEIN OVEREXPRESSED IN NON-P-GLYCOPROTEIN-CONTAINING MULTIDRUG-RESISTANT CELLS AND ITS RELATIONSHIP TO THE MRP GENE [J].
BARRAND, MA ;
HEPPELLPARTON, AC ;
WRIGHT, KA ;
RABBITTS, PH ;
TWENTYMAN, PR .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (02) :110-117
[4]   UNKNOTTING THE COMPLEXITIES OF MULTIDRUG RESISTANCE - THE INVOLVEMENT OF DNA TOPOISOMERASES IN DRUG-ACTION AND RESISTANCE [J].
BECK, WT .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1989, 81 (22) :1683-1685
[5]   EVALUATION OF GLUTATHIONE-S-TRANSFERASE-PI IN NONINVASIVE DUCTAL CARCINOMA OF BREAST [J].
BELLAMY, COC ;
HARRISON, DJ .
BRITISH JOURNAL OF CANCER, 1994, 69 (01) :183-185
[6]  
BORDOW SB, 1994, CANCER RES, V54, P5036
[7]  
BROCK I, 1995, CANCER RES, V55, P459
[8]   IMMUNOHISTOCHEMICAL DETECTION OF P-GLYCOPROTEIN - PROGNOSTIC CORRELATION IN SOFT-TISSUE SARCOMA OF CHILDHOOD [J].
CHAN, HSL ;
THORNER, PS ;
HADDAD, G ;
LING, V .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (04) :689-704
[9]   P-GLYCOPROTEIN EXPRESSION AS A PREDICTOR OF THE OUTCOME OF THERAPY FOR NEUROBLASTOMA [J].
CHAN, HSL ;
HADDAD, G ;
THORNER, PS ;
DEBOER, G ;
LIN, YP ;
ONDRUSEK, N ;
YEGER, H ;
LING, V .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (23) :1608-1614
[10]   QUANTITATIVE IMMUNOCYTOCHEMICAL ASSAYS OF P-GLYCOPROTEIN IN BREAST CARCINOMAS - CORRELATION TO MESSENGER-RNA EXPRESSION AND TO IMMUNOHISTOCHEMICAL PROGNOSTIC INDICATORS [J].
CHARPIN, C ;
VIELH, P ;
DUFFAUD, F ;
DEVICTOR, B ;
ANDRAC, L ;
LAVAUT, MN ;
ALLASIA, C ;
HORSCHOWSKI, N ;
PIANA, L .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (20) :1539-1545