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Altered glycosylation of proteins produced by malignant cells, and application for the diagnosis and immunotherapy of tumours

Most secretory and membrane‐bound proteins produced by mammalian cells contain covalently linked sugar chains. Alterations of the sugar chain structures of glycoproteins have been found to occur in various tumours. Because the sugar chains of glycoproteins are essential for the maintenance of the or...

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Published in:Immunology and cell biology 2005-08, Vol.83 (4), p.429-439
Main Authors: Kobata, Akira, Amano, Junko
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Language:English
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description Most secretory and membrane‐bound proteins produced by mammalian cells contain covalently linked sugar chains. Alterations of the sugar chain structures of glycoproteins have been found to occur in various tumours. Because the sugar chains of glycoproteins are essential for the maintenance of the ordered social behaviour of differentiated cells in multicellular organisms, alterations to the sugar chains are the molecular basis of abnormal social behaviours in tumour cells, such as invasion into the surrounding tissues and metastasis. In this review, the structure and enzymatic basis of typical alterations of the N‐linked sugar chains, which are found in various tumours, are introduced. These data are useful for devising diagnostic methods and immunotherapies for the clinical treatment of tumours. Three β‐N‐acetylglucosaminyltransferases, GnT‐III, ‐IV and ‐V, play roles in the structural alteration of the complex‐type sugar chains in various tumours. In addition, transcriptional changes in various glycosyltransferases, together with the transporters of sugar nucleotides and sulfate, which are responsible for the formation of the outer chain moieties of complex‐type sugar chains, are the keys to inducing the alterations.
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ispartof Immunology and cell biology, 2005-08, Vol.83 (4), p.429-439
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subjects Animals
Antigens, Tumor-Associated, Carbohydrate - chemistry
Antigens, Tumor-Associated, Carbohydrate - immunology
Carbohydrate Sequence
carcinoembryonic antigen
glycoproteins
Glycoproteins - chemistry
Glycoproteins - immunology
Glycoproteins - metabolism
Glycosylation
human chorionic gonadotropin
Humans
Immunotherapy
Molecular Sequence Data
N-Acetylglucosaminyltransferases - metabolism
Neoplasms - diagnosis
Neoplasms - immunology
Neoplasms - metabolism
Neoplasms - therapy
N‐linked sugar chain
trophoblastic diseases
γ‐glutamyltranspeptidase
title Altered glycosylation of proteins produced by malignant cells, and application for the diagnosis and immunotherapy of tumours
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