Expression of Sialyl-Tn antigen in breast cancer cells transfected with the human CMP-Neu5Ac:: GalNAc α2,6-sialyltransferase (ST6GalNAc 1) cDNA

被引:64
作者
Julien, S
Krzewinski-Recchi, MA
Harduin-Lepers, A
Gouyer, V
Huet, G
Le Bourhis, X
Delannoy, P [1 ]
机构
[1] Univ Sci & Technol Lille, Chim Biol Lab, CNRS, UMR 8576,Unite Glycobiol Struct & Fonct, F-59655 Villeneuve Dascq, France
[2] INSERM, U560, F-59045 Lille, France
[3] Univ Sci & Technol Lille, Dev Biol Lab, UPRES EA 1033, F-59655 Villeneuve Dascq, France
关键词
breast cancer; sialyl-Tn; ST6GalNAc; 1; O-glycosylation;
D O I
10.1023/A:1022200525695
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 GalNAcalpha-O-Ser/Thr. This reaction is mainly catalyzed by a CMP-Neu5Ac GalNAc alpha2,6-sialyltransferase: ST6GalNAc 1. In order to generate STn-positive breast cancer cells, we have cloned a cDNA encoding the full-lenght human ST6GaINAc I from HT-29-MTX cells. The stable transfection of MDA-MB-231 with an expression vector encoding ST6GaINAc 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.
引用
收藏
页码:883 / 893
页数:11
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