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Characterization and distribution of an oncofetal antigen (M2A antigen) expressed on testicular germ cell tumours

M2A antigen is an oncofetal antigen associated with germ cell neoplasia, present in testis on fetal gonocytes and re-expressed on carcinoma in situ (CIS) and germ cell tumours. We developed a panel of monoclonal antibodies (mAb), M2A (IgG2a), D1-26 (IgG2b) and D2-40 (IgG1), to this antigen in order...

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Autores principales: Marks, A, Sutherland, D R, Bailey, D, Iglesias, J, Law, J, Lei, M, Yeger, H, Banerjee, D, Baumal, R
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362349/
https://www.ncbi.nlm.nih.gov/pubmed/10408868
http://dx.doi.org/10.1038/sj.bjc.6690393
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author Marks, A
Sutherland, D R
Bailey, D
Iglesias, J
Law, J
Lei, M
Yeger, H
Banerjee, D
Baumal, R
author_facet Marks, A
Sutherland, D R
Bailey, D
Iglesias, J
Law, J
Lei, M
Yeger, H
Banerjee, D
Baumal, R
author_sort Marks, A
collection PubMed
description M2A antigen is an oncofetal antigen associated with germ cell neoplasia, present in testis on fetal gonocytes and re-expressed on carcinoma in situ (CIS) and germ cell tumours. We developed a panel of monoclonal antibodies (mAb), M2A (IgG2a), D1-26 (IgG2b) and D2-40 (IgG1), to this antigen in order to characterize its structure and study its distribution among germ cell tumours. M2A antigen was purified by sequential lectin and antibody affinity chromatography and characterized as a monomeric M(r) 40 000 surface sialoglycoprotein, extensively glycosylated with O-linked carbohydrate structures, but devoid of N-linked sugars. Terminal sialic acid residues were required for reactivity with mAb M2A and D1-26, but not D2-40. Sections of 69 testicular germ cell tumours, fixed in formalin and embedded in paraffin, were stained with mAb D2-40 to examine the distribution of M2A antigen. Uniform membrane staining was observed in seminomas, and focal staining in 69% of embryonal carcinomas, 29% of teratomas and 25% of yolk sac tumours. CIS in the vicinity of all germ cell tumours also displayed uniform membrane staining. The characterization of M2A antigen, and the development of mAb which react with it in conventionally preserved archival specimens, provide important initiatives to study the origin and progression of germ cell neoplasia. © 1999 Cancer Research Campaign
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spelling pubmed-23623492009-09-10 Characterization and distribution of an oncofetal antigen (M2A antigen) expressed on testicular germ cell tumours Marks, A Sutherland, D R Bailey, D Iglesias, J Law, J Lei, M Yeger, H Banerjee, D Baumal, R Br J Cancer Regular Article M2A antigen is an oncofetal antigen associated with germ cell neoplasia, present in testis on fetal gonocytes and re-expressed on carcinoma in situ (CIS) and germ cell tumours. We developed a panel of monoclonal antibodies (mAb), M2A (IgG2a), D1-26 (IgG2b) and D2-40 (IgG1), to this antigen in order to characterize its structure and study its distribution among germ cell tumours. M2A antigen was purified by sequential lectin and antibody affinity chromatography and characterized as a monomeric M(r) 40 000 surface sialoglycoprotein, extensively glycosylated with O-linked carbohydrate structures, but devoid of N-linked sugars. Terminal sialic acid residues were required for reactivity with mAb M2A and D1-26, but not D2-40. Sections of 69 testicular germ cell tumours, fixed in formalin and embedded in paraffin, were stained with mAb D2-40 to examine the distribution of M2A antigen. Uniform membrane staining was observed in seminomas, and focal staining in 69% of embryonal carcinomas, 29% of teratomas and 25% of yolk sac tumours. CIS in the vicinity of all germ cell tumours also displayed uniform membrane staining. The characterization of M2A antigen, and the development of mAb which react with it in conventionally preserved archival specimens, provide important initiatives to study the origin and progression of germ cell neoplasia. © 1999 Cancer Research Campaign Nature Publishing Group 1999-05 1999-05-01 /pmc/articles/PMC2362349/ /pubmed/10408868 http://dx.doi.org/10.1038/sj.bjc.6690393 Text en Copyright © 1999 Cancer Research Campaign 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 Regular Article
Marks, A
Sutherland, D R
Bailey, D
Iglesias, J
Law, J
Lei, M
Yeger, H
Banerjee, D
Baumal, R
Characterization and distribution of an oncofetal antigen (M2A antigen) expressed on testicular germ cell tumours
title Characterization and distribution of an oncofetal antigen (M2A antigen) expressed on testicular germ cell tumours
title_full Characterization and distribution of an oncofetal antigen (M2A antigen) expressed on testicular germ cell tumours
title_fullStr Characterization and distribution of an oncofetal antigen (M2A antigen) expressed on testicular germ cell tumours
title_full_unstemmed Characterization and distribution of an oncofetal antigen (M2A antigen) expressed on testicular germ cell tumours
title_short Characterization and distribution of an oncofetal antigen (M2A antigen) expressed on testicular germ cell tumours
title_sort characterization and distribution of an oncofetal antigen (m2a antigen) expressed on testicular germ cell tumours
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362349/
https://www.ncbi.nlm.nih.gov/pubmed/10408868
http://dx.doi.org/10.1038/sj.bjc.6690393
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