TY - JOUR
T1 - The human epithelial carcinoma antigen recognized by monoclonal antibody AE3 is expressed on a sulfoglycolipid in addition to neoplastic mucins
AU - Palma, Angelina S.
AU - Liu, Yan
AU - Childs, Robert A.
AU - Herbert, Colin
AU - Wang, Denong
AU - Chai, Wengang
AU - Feizi, Ten
N1 - This work has been supported by National Cancer Institute Alliance of Glyco-biologists for Detection of Cancer and Cancer Risk (U01 CA128416); 'UK Research Councils' Basic Technology Initiative 'Glycoarrays' (GRS/79268) and EPSRC Translational Grant (EP/G037604/1). ASP is a fellow of the Fundacao para a Ciencia e Tecnologia (SFRH/BPD/26515/2006, Portugal).
PY - 2011/5/20
Y1 - 2011/5/20
N2 - The term human epithelial carcinoma antigen (HCA) has been applied collectively to mucin-type high molecular weight (>1000kDa) glycoproteins that are over-expressed in epithelial cancers. Since the 1990s, over 40 monoclonal antibodies have been raised that recognize HCA. There has been evidence that the antigenic determinants are mostly carbohydrates, but details have been elusive. Here we have carried out carbohydrate microarray analyses of one of the monoclonal antibodies, AE3, that has been regarded the 'most carcinoma specific' in respect to its ability to detect HCA in sera of patients with epithelial cancers. The microarrays encompassed a series of 492 sequence-defined glycan probes in the form of glycolipids and neoglycolipids. We have thus established that the antigen recognized by antibody AE3 is a carbohydrate sequence distinct from the A, B, H, Lewisa/b, Lewisx/y and T antigens, but that it is strongly expressed on the monosulfated tetra-glycosyl ceramide, SM1a, Galβ1-3GalNAcβ1-4(3-O-sulfate)Galβ1-4GlcCer. This is the first report of an anti-HCA to be characterized with respect to its recognition sequence and of the occurrence of the antigen on a glycolipid as well as on glycoproteins. Knowledge of a discrete glycan sequence as target antigen now opens the way to its exploration as a serologic cancer biomarker, namely to determine if the antigen elicits an autoantibody response in early non-metastatic cancer, or if it is shed and immunochemically detectable in more advanced disease.
AB - The term human epithelial carcinoma antigen (HCA) has been applied collectively to mucin-type high molecular weight (>1000kDa) glycoproteins that are over-expressed in epithelial cancers. Since the 1990s, over 40 monoclonal antibodies have been raised that recognize HCA. There has been evidence that the antigenic determinants are mostly carbohydrates, but details have been elusive. Here we have carried out carbohydrate microarray analyses of one of the monoclonal antibodies, AE3, that has been regarded the 'most carcinoma specific' in respect to its ability to detect HCA in sera of patients with epithelial cancers. The microarrays encompassed a series of 492 sequence-defined glycan probes in the form of glycolipids and neoglycolipids. We have thus established that the antigen recognized by antibody AE3 is a carbohydrate sequence distinct from the A, B, H, Lewisa/b, Lewisx/y and T antigens, but that it is strongly expressed on the monosulfated tetra-glycosyl ceramide, SM1a, Galβ1-3GalNAcβ1-4(3-O-sulfate)Galβ1-4GlcCer. This is the first report of an anti-HCA to be characterized with respect to its recognition sequence and of the occurrence of the antigen on a glycolipid as well as on glycoproteins. Knowledge of a discrete glycan sequence as target antigen now opens the way to its exploration as a serologic cancer biomarker, namely to determine if the antigen elicits an autoantibody response in early non-metastatic cancer, or if it is shed and immunochemically detectable in more advanced disease.
KW - Anti-epiglycanin AE3
KW - Epithelial mucin glycoproteins
KW - Human carcinoma antigen HCA
KW - MUC21
KW - NGL-based carbohydrate microarrays
KW - Sulfoglycolipids
UR - http://www.scopus.com/inward/record.url?scp=79956196885&partnerID=8YFLogxK
U2 - 10.1016/j.bbrc.2011.04.055
DO - 10.1016/j.bbrc.2011.04.055
M3 - Article
C2 - 21527252
AN - SCOPUS:79956196885
SN - 0006-291X
VL - 408
SP - 548
EP - 552
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 4
ER -