Recognition of an epitope of a breast cancer antigen by human antibody

被引:13
作者
Cao, JN
Gao, TW
Giuliano, AE
Irie, RF
机构
[1] St Johns Hlth Ctr, John Wayne Canc Inst, Dept Biotechnol Sci, Santa Monica, CA 90404 USA
[2] St Johns Hlth Ctr, John Wayne Canc Inst, Roy E Coats Res Labs, Santa Monica, CA 90404 USA
关键词
human antibody; antigen epitope; breast cancer; peptide; retinoblastoma binding protein 1;
D O I
10.1023/A:1006115922401
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A novel tumor-associated peptide epitope KASIFLK expressed preferentially by breast cancer cells was identified using an IgG antibody from a breast cancer patient. A cDNA library from a MCF-7 breast cancer cell line was screened to isolate three cDNA clones that were immunoreactive with this antibody. KASIFLK was located in clones 27 and 40, both of which were identical to the cDNA and protein sequence of retinoblastoma binding protein 1 (RBP1, 250-256). An affinity-purified IgG antibody against the peptide epitope was completely absorbed by cytoplasmic extracts of MCF-7 cells. Immunohistochemical staining using this antibody revealed the antigen in MCF-7 cells and in 12 of 15 primary breast cancer tissues and 3 of 34 other cancer tissues, but in none of 6 normal breast tissues. Anti-KASIFLK antibody titers were significantly higher in sera of 55 breast cancer patients than in sera from 30 normal healthy donors (P > 0.001). These results suggest that KASIFLK or its cross-reactive epitope is a breast cancer antigen and is immunogenic in humans.
引用
收藏
页码:279 / 290
页数:12
相关论文
共 26 条
[1]   PREVALENCE OF SERUM ANTIBODIES AGAINST THE P53 TUMOR-SUPPRESSOR GENE PROTEIN IN VARIOUS CANCERS [J].
ANGELOPOULOU, K ;
DIAMANDIS, EP ;
SUTHERLAND, DJA ;
KELLEN, JA ;
BUNTING, PS .
INTERNATIONAL JOURNAL OF CANCER, 1994, 58 (04) :480-487
[2]   THE RETINOBLASTOMA PROTEIN COPURIFIES WITH E2F-I, AN E1A-REGULATED INHIBITOR OF THE TRANSCRIPTION FACTOR E2F [J].
BAGCHI, S ;
WEINMANN, R ;
RAYCHAUDHURI, P .
CELL, 1991, 65 (06) :1063-1072
[3]   IMMUNITY TO ONCOGENIC PROTEINS [J].
CHEEVER, MA ;
DISIS, ML ;
BERNHARD, H ;
GRALOW, JR ;
HAND, SL ;
HUSEBY, ES ;
QIN, HL ;
TAKAHASHI, M ;
CHEN, W .
IMMUNOLOGICAL REVIEWS, 1995, 145 :33-59
[4]   ABERRANT SUBCELLULAR-LOCALIZATION OF BRCA1 IN BREAST-CANCER [J].
CHEN, YM ;
CHEN, CF ;
RILEY, DJ ;
ALLRED, DC ;
CHEN, PL ;
VONHOFF, D ;
OSBORNE, CK ;
LEE, WH .
SCIENCE, 1995, 270 (5237) :789-791
[5]   SV40 LARGE TUMOR-ANTIGEN FORMS A SPECIFIC COMPLEX WITH THE PRODUCT OF THE RETINOBLASTOMA SUSCEPTIBILITY GENE [J].
DECAPRIO, JA ;
LUDLOW, JW ;
FIGGE, J ;
SHEW, JY ;
HUANG, CM ;
LEE, WH ;
MARSILIO, E ;
PAUCHA, E ;
LIVINGSTON, DM .
CELL, 1988, 54 (02) :275-283
[6]   CLONING OF CDNAS FOR CELLULAR PROTEINS THAT BIND TO THE RETINOBLASTOMA GENE-PRODUCT [J].
DEFEOJONES, D ;
HUANG, PS ;
JONES, RE ;
HASKELL, KM ;
VUOCOLO, GA ;
HANOBIK, MG ;
HUBER, HE ;
OLIFF, A .
NATURE, 1991, 352 (6332) :251-254
[7]  
DISIS ML, 1994, CANCER RES, V54, P16
[8]   THE HUMAN PAPILLOMA VIRUS-16 E7-ONCOPROTEIN IS ABLE TO BIND TO THE RETINOBLASTOMA GENE-PRODUCT [J].
DYSON, N ;
HOWLEY, PM ;
MUNGER, K ;
HARLOW, E .
SCIENCE, 1989, 243 (4893) :934-937
[9]   LARGE T-ANTIGENS OF MANY POLYOMAVIRUSES ARE ABLE TO FORM COMPLEXES WITH THE RETINOBLASTOMA PROTEIN [J].
DYSON, N ;
BERNARDS, R ;
FRIEND, SH ;
GOODING, LR ;
HASSELL, JA ;
MAJOR, EO ;
PIPAS, JM ;
VANDYKE, T ;
HARLOW, E .
JOURNAL OF VIROLOGY, 1990, 64 (03) :1353-1356
[10]  
FATTAEY AR, 1993, ONCOGENE, V8, P3149