Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1999 May;80(3-4):569-78.
doi: 10.1038/sj.bjc.6690393.

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

Affiliations

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

A Marks et al. Br J Cancer. 1999 May.

Abstract

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, 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.

PubMed Disclaimer

References

    1. J Biol Chem. 1974 Feb 10;249(3):811-7 - PubMed
    1. Int J Androl. 1996 Dec;19(6):365-70 - PubMed
    1. J Biol Chem. 1982 Sep 25;257(18):10766-9 - PubMed
    1. J Immunol. 1984 Jul;133(1):327-33 - PubMed
    1. J Biol Chem. 1984 Sep 10;259(17):10700-4 - PubMed

Publication types

MeSH terms