Glycobiology Advance Access first published online on August 31, 2005
This version published online on September 6, 2005
Glycobiology, doi:10.1093/glycob/cwj033
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1 Unité de Glycobiologie Structurale et Fonctionnelle, UMR CNRS n°8576, GDR CNRS n°2590, Université des Sciences et Technologies de Lille, F-59655 Villeneuve d’Ascq, France
* To whom correspondence should be addressed. Sialyl-Tn is a carbohydrate antigen over-expressed in several epithelial cancers, including breast cancer, and usually associated with poor prognosis. Sialyl-Tn is synthesized by a CMP-Neu5Ac:GalNAc
Received July 6, 2005
Revised August 23, 2005
Accepted August 24, 2005
Article
ST6GalNAc I expression in MDA-MB-231 breast cancer cells greatly modifies their O-glycosylation pattern and enhances their tumourigenicity
2 Laboratoire de Biologie du Développement, ERI8, UPRES EA 1033, Université des Sciences et Technologies de Lille, F-59655 Villeneuve d’Ascq, France
3 Center of Biochemistry, Medical Faculty, and Center for Molecular Medicine Cologne, University of Cologne, Joseph-Stelzmann-Str. 52, D-50931 Cologne
4 Centre Commun de Mesures Imagerie Cellulaire, Université des Sciences et Technologies de Lille, F-59655 Villeneuve d’Ascq, France
5 Unité de Glycobiologie Structurale et Fonctionnelle, UMR CNRS n°8576, GDR CNRS n°2590, Université des Sciences et Technologies de Lille, F-59655 Villeneuve d’Ascq, France.
P. Delannoy, E-mail: Philippe.Delannoy{at}univ-lille1.fr
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Abstract
2,6-sialyltransferase: ST6GalNAc I, which transfers a sialic acid residue in
2,6-linkage to the GalNAca1-O-Ser/Thr structure. However, established breast cancer cell lines express neither ST6GalNAc I nor sialyl-Tn. We have previously shown that stable transfection of MDA-MB-231, a human breast cancer cell line, with ST6GalNAc I cDNA induces sialyl-Tn antigen expression. We report here the modifications of the O-glycosylation pattern of a MUC1 related recombinant protein secreted by MDA-MB-231 sialyl-Tn positive cells. We also show that sialyl-Tn expression and concomitant changes in the overall O-glycan profiles induce a decrease of adhesion and an increase of migration of MDA-MB-231. Moreover, STn positive clones exhibit an increased tumour growth in SCID mice. These observations suggest that modification of the O-glycosylation pattern induced by ST6GalNAc I expression are sufficient to enhance the tumourigenicity of MDA-MB-231 breast cancer cells.
The author order has been corrected.
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