Monoclonal antibodies reactive with mucin expressed in breast cancer View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

1989-06

AUTHORS

P-X Xing, JJ Tjandra, SA Stacker, JG Teh, CH Thompson, PJ McLaughlin, IFC McKenzie

ABSTRACT

Three murine monoclonal antibodies (BC1, BC2 and BC3) were developed against human milk fat globule membrane (HMFGM). By immunoperoxidase staining, it was found that the antigenic determinants had a predominant distribution in breast cancer tissue. In addition, the antibodies reacted preferentially with mucin derived from human milk rather than that derived from the breast cancer cell line ZR75; they also recognized polymorphic high molecular weight components (MW greater than or equal to 230,000) in serum and in human milk fat globule membrane. Thus the antibodies appear to react with a component of the family of mucins found in breast cancer and human milk and it appears likely that at least part of each epitope is protein in nature. Antibodies BC1, BC2 and BC3 recognized related but not identical epitopes, and they appear to be co-expressed on the same molecules as 3E1.2-defined antigen (mammary serum antigen, MSA) which is also a member of the family of breast cancer-related mucin. However, the 3E1.2 epitope is distinct and non-cross-reactive with those described for BC1, BC2 and BC3. The BC2 and BC3 defined epitopes were examined for their value in serum assays. Immunoassay was developed with a combination of two antibodies, using antibody BC3 for antigen capture and antibody BC2 or 3E1.2 for antigen detection and gave reasonable sensitivity (approximately 85%) and specificity (approximately 95%) in such serum tests for breast cancer. In a limited study, these tests appeared to complement the MSA test in the detection of breast cancer. More... »

PAGES

icb198929

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/icb.1989.29

DOI

http://dx.doi.org/10.1038/icb.1989.29

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1025446450

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/2477330


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