1. Academic Validation
  2. Expression of sialyl-Tn antigen in breast cancer cells transfected with the human CMP-Neu5Ac: GalNAc alpha2,6-sialyltransferase (ST6GalNac I) cDNA

Expression of sialyl-Tn antigen in breast cancer cells transfected with the human CMP-Neu5Ac: GalNAc alpha2,6-sialyltransferase (ST6GalNac I) cDNA

  • Glycoconj J. 2001 Nov-Dec;18(11-12):883-93. doi: 10.1023/a:1022200525695.
S Julien 1 M A Krzewinski-Recchi A Harduin-Lepers V Gouyer G Huet X Le Bourhis P Delannoy
Affiliations

Affiliation

  • 1 Unité de Glycobiologie Structurale et Fonctionnelle, UMR CNRS no 8576, Laboratoire de Chimie Biologique, Université des Sciences et Technologies de Lille, F-59655 Villeneuve d'Ascq, France.
Abstract

Sialyl-Tn antigen (STn) is a Cancer associated carbohydrate antigen over-expressed in several cancers including breast Cancer, and currently associated with more aggressive diseases and poor prognosis. However, the commonly used breast Cancer cell lines (MDA-MB-231, T47-D and MCF7) do not express STn antigen. The key step in the biosynthesis of STn is the transfer of a sialic acid residue in alpha2,6-linkage to GalNAc alpha-O-Ser/Thr. This reaction is mainly catalyzed by a CMP-Neu5Ac GalNAc alpha2,6-sialyltransferase: ST6GalNAc I. In order to generate STn-positive breast Cancer cells, we have cloned a cDNA encoding the full-length human ST6GalNAc I from HT-29-MTX cells. The stable transfection of MDA-MB-231 with an expression vector encoding ST6GalNAc I induces the expression of STn antigen at the cell surface. The expression of STn short cuts the initial O-glycosylation pattern of these cell lines, by competing with the Core-1 beta1,3-galactosyltransferase, the first Enzyme involved in the elongation of O-glycan chains. Moreover, we show that STn expression is associated with morphological changes, decreased growth and increased migration of MDA-MB-231 cells.

Figures
Products