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Similarity and co-expression of tumour-associated antigens recognised by different monoclonal antibodies.

The concentration of carcinoembryonic antigen (CEA), CA130, CA125, SLX, CA19-9, SPan1, and tumour-associated glycoprotein 72 (TAG-72) in the culture supernatant of 15 cancer cell lines and in the sera of 58 cancer patients was measured, and the co-expression of these antigens was examined by double...

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Autores principales: Sakahara, H., Saga, T., Endo, K., Kousaka, T., Hosono, M., Kobayashi, H., Shirato, M., Konishi, J.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1993
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968720/
https://www.ncbi.nlm.nih.gov/pubmed/8217607
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author Sakahara, H.
Saga, T.
Endo, K.
Kousaka, T.
Hosono, M.
Kobayashi, H.
Shirato, M.
Konishi, J.
author_facet Sakahara, H.
Saga, T.
Endo, K.
Kousaka, T.
Hosono, M.
Kobayashi, H.
Shirato, M.
Konishi, J.
author_sort Sakahara, H.
collection PubMed
description The concentration of carcinoembryonic antigen (CEA), CA130, CA125, SLX, CA19-9, SPan1, and tumour-associated glycoprotein 72 (TAG-72) in the culture supernatant of 15 cancer cell lines and in the sera of 58 cancer patients was measured, and the co-expression of these antigens was examined by double determinant immunoradiometric assays. The high correlation coefficient of the concentrations and significant binding in the double determinant assays indicated a close relationship between CA125 and CA130 and between CA19-9 and SPan1. There was variable binding of the 125I-labelled anti-SLX, anti-CA19-9, and anti-SPan1 antibodies to anti-CA130 beads that had been pre-incubated with the culture supernatants, suggesting the presence of the epitopes of SLX, CA19-9, and SPan1 on the molecule expressing CA130. Similarly, the epitopes of SLX, CA19-9, and SPan1 could be present on the molecule expressing CEA. 125I-labelled anti-CA19-9, anti-SLX, and anti-TAG-72 antibodies were bound in variable proportions to anti-CA130 beads or to anti-CEA beads that had been pre-incubated with patients' sera. However, CEA and CA130 were not expressed on the same molecule, either in the culture supernatant, or in patients' sera. In conclusion, the carbohydrate epitopes of CA19-9, SPan1, SLX, and TAG-72 could be present on the molecule recognised by the anti-CA130 or anti-CEA antibody; however, the epitopes of CA130 and CEA did not co-exist on the same molecule.
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spelling pubmed-19687202009-09-10 Similarity and co-expression of tumour-associated antigens recognised by different monoclonal antibodies. Sakahara, H. Saga, T. Endo, K. Kousaka, T. Hosono, M. Kobayashi, H. Shirato, M. Konishi, J. Br J Cancer Research Article The concentration of carcinoembryonic antigen (CEA), CA130, CA125, SLX, CA19-9, SPan1, and tumour-associated glycoprotein 72 (TAG-72) in the culture supernatant of 15 cancer cell lines and in the sera of 58 cancer patients was measured, and the co-expression of these antigens was examined by double determinant immunoradiometric assays. The high correlation coefficient of the concentrations and significant binding in the double determinant assays indicated a close relationship between CA125 and CA130 and between CA19-9 and SPan1. There was variable binding of the 125I-labelled anti-SLX, anti-CA19-9, and anti-SPan1 antibodies to anti-CA130 beads that had been pre-incubated with the culture supernatants, suggesting the presence of the epitopes of SLX, CA19-9, and SPan1 on the molecule expressing CA130. Similarly, the epitopes of SLX, CA19-9, and SPan1 could be present on the molecule expressing CEA. 125I-labelled anti-CA19-9, anti-SLX, and anti-TAG-72 antibodies were bound in variable proportions to anti-CA130 beads or to anti-CEA beads that had been pre-incubated with patients' sera. However, CEA and CA130 were not expressed on the same molecule, either in the culture supernatant, or in patients' sera. In conclusion, the carbohydrate epitopes of CA19-9, SPan1, SLX, and TAG-72 could be present on the molecule recognised by the anti-CA130 or anti-CEA antibody; however, the epitopes of CA130 and CEA did not co-exist on the same molecule. Nature Publishing Group 1993-11 /pmc/articles/PMC1968720/ /pubmed/8217607 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Sakahara, H.
Saga, T.
Endo, K.
Kousaka, T.
Hosono, M.
Kobayashi, H.
Shirato, M.
Konishi, J.
Similarity and co-expression of tumour-associated antigens recognised by different monoclonal antibodies.
title Similarity and co-expression of tumour-associated antigens recognised by different monoclonal antibodies.
title_full Similarity and co-expression of tumour-associated antigens recognised by different monoclonal antibodies.
title_fullStr Similarity and co-expression of tumour-associated antigens recognised by different monoclonal antibodies.
title_full_unstemmed Similarity and co-expression of tumour-associated antigens recognised by different monoclonal antibodies.
title_short Similarity and co-expression of tumour-associated antigens recognised by different monoclonal antibodies.
title_sort similarity and co-expression of tumour-associated antigens recognised by different monoclonal antibodies.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968720/
https://www.ncbi.nlm.nih.gov/pubmed/8217607
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