Glycobiology Advance Access published online on September 28, 2005
Glycobiology, doi:10.1093/glycob/cwj045
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 Dipartimento di Patologia Sperimentale, Università di Bologna, Via S. Giacomo 14, 40126 Bologna, Italy
* To whom correspondence should be addressed.
Received August 2, 2005
Revised September 19, 2005
Accepted September 20, 2005
Article
Phenotypic changes induced by expression of
-galactoside
2,6 sialyltransferase (ST6Gal.I) in the human colon cancer cell line SW948
Fabio Dall'Olio, E-mail: fabio.dallolio{at}unibo.it
![]()
Abstract
-Galactoside
2,6 sialyltransferase (ST6Gal.I), the enzyme which adds sialic acid in
2,6-linkage on lactosaminic termini of glycoproteins, is frequently overexpressed in cancer but its relationship with malignancy remains unclear. In this study, we have investigated the phenotypic changes induced by the expression of
2,6-sialylated lactosaminic chains in the human colon cancer cell line SW948 which was originally devoid of ST6Gal.I. Clones derived from transfection with the ST6Gal.I cDNA were compared with untransfected cells and mock-transfectants. The ST6Gal.I-expressing clones show: 1) increased adherence to fibronectin and collagen IV but not to hyaluronic acid. Treatment with Clostridium perfrigens neuraminidase reduces the binding to fibronectin and collagen IV of ST6Gal.I-expressing cells but not that of ST6Gal.I-negative cells; 2) accumulation and more focal distribution of
1 integrins on the cell surface; 3) different distribution of actin fibers; 4) flatter morphology and reduced tendency to multilayer growth; 5) improved ability to heal a scratch wound; 6) reduced ability to grow at the subcutaneous site of injection in nude mice. Our data suggest that the presence of
2,6-linked sialic acid on membrane glycoconjugates increases the binding to extracellular matrix components, resulting in a membrane stabilization of
1 integrins, further strengthening the binding. This mechanism can provide a basis for the flatter morphology and the reduced tendency to multilayer growth, resulting in a more ordered tissue organization. These data indicate that in the cell line SW948, the effect of ST6Gal.I expression is consistent with the attenuation of the neoplastic phenotype.![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
N. Malagolini, M. Chiricolo, M. Marini, and F. Dall'Olio Exposure of {alpha}2,6-sialylated lactosaminic chains marks apoptotic and necrotic death in different cell types Glycobiology, February 1, 2009; 19(2): 172 - 181. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Lee, H.-J. Lee, S. Bae, and Y.-S. Lee Protein Sialylation by Sialyltransferase Involves Radiation Resistance Mol. Cancer Res., August 1, 2008; 6(8): 1316 - 1325. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Hedlund, E. Ng, A. Varki, and N. M. Varki {alpha}2-6 Linked Sialic Acids on N-Glycans Modulate Carcinoma Differentiation In vivo Cancer Res., January 15, 2008; 68(2): 388 - 394. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Malagolini, D. Santini, M. Chiricolo, and F. Dall'Olio Biosynthesis and expression of the Sda and sialyl Lewis x antigens in normal and cancer colon Glycobiology, July 1, 2007; 17(7): 688 - 697. [Abstract] [Full Text] [PDF] |
||||


