Abstract |
Our previous study showed that the gene expression of beta-1,4-galactosyltransferase V (beta-1,4-GalT V), preferentially galactosylating GlcNAc1-->6Man of oligosaccharides, increased in the process of astrocytoma progress, with the highest level in grade IV astrocytoma. To investigate the function of this beta-1,4-GalT in cell proliferation, the sense and antisense cDNA of beta-1,4-GalT V was constructed as pcDNA3-HA-GalT V and pcDNA3-anti-GalT V respectively and transfected into SHG cell, a kind of human astrocytoma cell line. The transfection was confirmed with Northern and Western blot assay. It was found that the growth of SHG/HA-GalT V in serum-containing medium was faster than that of mock-transfectant with the vector pcDNA3, whereas the growth of SHG/GalTV-AS was slower than that of mock-transfectant. GalTV-HA/SHG showed a stronger capability for colony formation than that of GalTV-AS/SHG as evaluated by anchorage-independent growth in soft agar assay. This result was consistent with that of the growth curve. By RCA-1 lectin assay, the galactosylation on the surface of GalTV-HA/SHG and SHG/GalTV-AS was stained stronger (P<0.001) and weaker (P<0.05) respectively compared with the mock transfectant. This indicates that beta-1,4-GalT V was involved in the malignant phenotype of astrocytoma cells, possibly causing the high galactosylation on the cell surface.
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Authors | S Xu, S Zhang, C Chen, J Yan, M Cai, X Zhu, J Gu |
Journal | Journal of experimental & clinical cancer research : CR
(J Exp Clin Cancer Res)
Vol. 21
Issue 3
Pg. 409-14
(Sep 2002)
ISSN: 0392-9078 [Print] England |
PMID | 12385586
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Lectins
- Galactosyltransferases
- beta-1,4-galactosyltransferase V
- Galactose
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Topics |
- Astrocytoma
(enzymology, pathology)
- Blotting, Northern
- Blotting, Western
- Brain Neoplasms
(enzymology, pathology)
- Cell Division
- Colony-Forming Units Assay
- Galactose
(metabolism)
- Galactosyltransferases
(metabolism)
- Gene Expression Regulation, Neoplastic
- Humans
- Lectins
(metabolism)
- Plasmids
- Transfection
- Tumor Cells, Cultured
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