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. 1995 Feb;40(2):132-7.
doi: 10.1007/BF01520296.

Expression of monoclonal-antibody-defined antigens in fractions isolated from human breast carcinomas and patients' serum

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Expression of monoclonal-antibody-defined antigens in fractions isolated from human breast carcinomas and patients' serum

M V Croce et al. Cancer Immunol Immunother. 1995 Feb.

Abstract

The aim of this study was to examine tissue from patients with breast carcinoma or benign breast disease for the presence of monoclonal-antibody-defined antigens, including the MUC1 mucin and carcinoembryonic antigen CEA. The tests were performed by sodium dodecyl sulphate/polyacrylamide gel electrophoretic separation of proteins, electrophoretic transfer to nitrocellulose membranes and immunostaining with the monoclonal antibodies. Some of the antigens identified are known to circulate at high levels in some but not necessarily all, breast carcinoma patients. Serum from a panel of ten breast cancer patients was subjected to a fractionation procedure designed to release antigen from immune complexes, and again these samples were analysed for the presence of monoclonal-antibody-defined antigens. A high frequency of positive reactions was detected by the anti-MUC1 monoclonal antibody C595 with both breast carcinoma subcellular membrane fractions as well as antigen fractions eluted from circulating immune complexes. No reactions were observed with equivalent materials from benign breast disease samples. The findings illustrate the variability in antigen expression between breast tumours. The data also indicate that a proportion of patients respond to their tumour by the production of antibodies that recognise the MUC1 antigen in their circulation.

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References

    1. Abecassis J, Petit JC, Eber M, Klein T, Rodier D, Jauser JC, Methlin G. Complexes immuns circulants dans le cancer du sein. Bull Cancer (Paris) 1985;72:42. - PubMed
    1. Beard D, Haskell C. Carcinoembryonic antigen in breast cancer. Am J Med. 1986;80:241. - PubMed
    1. Bocker W, Schweikart G, Pollow K. Immunohistochemical demonstration of carcinoembryonic (CEA) in 120 mammary carcinomas and its correlation with tumor type, grading, staging, plasma-CEA and biochemical receptor status. Pathol Res Pract. 1985;180:490. - PubMed
    1. Brown A, Feizi T, Gooi HC, Embleton M, Picard J, Baldwin RW. A monoclonal antibody against human colonic adenoma recognizes difucosylated type-2 blood group chains. Biosci Rep. 1983;3:163. - PubMed
    1. Creighton WD, Lambert PH, Miescher PA. Detection of antibodies and soluble antigen-antibody complexes by precipitation with polyethylene glycol. J Immunol. 1973;11:1219. - PubMed

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