Carcinoma-associated MUC1 detected by immunoradiometric assays

被引:15
作者
Norum, LF [1 ]
Varaas, T [1 ]
Kierulf, B [1 ]
Nustad, K [1 ]
机构
[1] Norwegian Radium Hosp, Cent Lab, N-0310 Oslo, Norway
关键词
MUC1; immunoassay; monoclonal antibodies; antibody specificity;
D O I
10.1159/000056515
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Fifty-four anti-MUC1 antibodies submitted to the International Society for Oncodevelopmental Biology and Medicine (ISOBM) Workshop (TD-4) were evaluated in immunoradiometric assays, using sera from carcinoma patients and healthy donors. The carcinoma serum pool contained sera from 30 patients with advanced cancer(10 breast, 10 colon, and 10 ovarian). This serum pool contained 696 kU/l MUC1, 770 mu g/l CEA, and 3,700 kU/l CA 125. The reference serum pool was obtained from IO healthy women combined with 20 sera from pregnant women, of which half had elevated CA 125 (range 82-254 kU/l). The reference serum pool contained 13 kU/l MUC1, 2 mu g/l CEA, and 65 kU/l CA 125. The Workshop antibodies were tested both as solid-phase antibodies and as tracer antibodies with the carcinoma serum pool. Twenty-two tracer antibodies and 38 solid-phase antibodies gave at least one combination with >10% binding of the tracer antibody for a total of 836 combinations. These were tested further with the reference serum pool. Antibodies used as tracers could be separated into three categories: Group 1 antibodies, MF06, MF11, B27.29, MF30, and Ma552, gave mainly 'carcinoma-specific' assays in combinations with the solid-phase antibodies, i.e. binding ratio between carcinoma MUC1 and reference MUC1 >10. Group 2 antibodies, DF3, 7540MR, A76-A/C7, BC4N154, M38, 7539MR, B12, GP1.4, 232A1, Mc5, and Ma695 gave both 'specific' and 'nonspecific' binding ratios depending on the solid-phase antibody used. Group 3 antibodies, 214D4, BC4E549, E29, BCP8, BC3, and 3E1.2, gave mainly 'nonspecific' combinations, i.e. ratios less than or equal to 10. All antibodies used to capture MUC1 on the solid phase gave both 'specific' and `nonspecific' combinations depending on the tracer antibody used. Ten antibodies were clearly more efficient as solid-phase capture antibodies; Ma695, B12, M38, GP1.4, 214D4, MF06, B27.29, A76-A/C7, BC3, and KC4. Our findings indicate that the ability to detect 'carcinoma-specific MUC1' cannot be deduced from epitope specificity alone.
引用
收藏
页码:134 / 146
页数:13
相关论文
共 36 条
[1]  
ANDREW SM, 1996, CURRENT PROTOCOLS IM
[2]  
BORMER OP, 1990, J IMMUNOL METHODS, V127, P171
[3]  
BRAY KR, 1987, CANCER RES, V47, P5853
[4]   MECHANISMS UNDERLYING ABERRANT GLYCOSYLATION OF MUC1 MUCIN IN BREAST-CANCER CELLS [J].
BROCKHAUSEN, I ;
YANG, JM ;
BURCHELL, J ;
WHITEHOUSE, C ;
TAYLORPAPADIMITRIOU, J .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 233 (02) :607-617
[5]  
Brown J P, 1990, Immunol Ser, V53, P69
[6]   A SHORT SEQUENCE, WITHIN THE AMINO-ACID TANDEM REPEAT OF A CANCER-ASSOCIATED MUCIN, CONTAINS IMMUNODOMINANT EPITOPES [J].
BURCHELL, J ;
TAYLORPAPADIMITRIOU, J ;
BOSHELL, M ;
GENDLER, S ;
DUHIG, T .
INTERNATIONAL JOURNAL OF CANCER, 1989, 44 (04) :691-696
[7]  
BURCHELL J, 1993, EPITHELIAL CELL BIOL, V2, P155
[8]   DETECTION OF THE TUMOR-ASSOCIATED ANTIGENS RECOGNIZED BY THE MONOCLONAL-ANTIBODIES HMFG-1 AND HMFG-2 IN SERUM FROM PATIENTS WITH BREAST-CANCER [J].
BURCHELL, J ;
WANG, D ;
TAYLORPAPADIMITRIOU, J .
INTERNATIONAL JOURNAL OF CANCER, 1984, 34 (06) :763-768
[9]   EPITHELIAL MUCIN CORE ANTIGEN (EMCA) IN ASSESSING THERAPEUTIC RESPONSE IN ADVANCED BREAST-CANCER - A COMPARISON WITH CA15.3 [J].
DIXON, AR ;
PRICE, MR ;
HAND, CW ;
SIBLEY, PEC ;
SELBY, C ;
BLAMEY, RW .
BRITISH JOURNAL OF CANCER, 1993, 68 (05) :947-949
[10]  
FRENGEN J, 1993, CLIN CHEM, V39, P2174