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Role of GalNAc4S-6ST in Astrocytic Tumor Progression

N-Acetylgalactosamine 4-sulfate 6-O-sulfotransferase (GalNAc4S-6ST) is the sulfotransferase responsible for biosynthesis of highly sulfated chondroitin sulfate CS-E. Although involvements of CS-E in neuronal cell functions have been extensively analyzed, the role of GalNAc4S-6ST in astrocytic tumor...

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Autores principales: Kobayashi, Tatsuya, Yan, Huimin, Kurahashi, Yasuhiro, Ito, Yuki, Maeda, Hiroshi, Tada, Tsuyoshi, Hongo, Kazuhiro, Nakayama, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3547881/
https://www.ncbi.nlm.nih.gov/pubmed/23349846
http://dx.doi.org/10.1371/journal.pone.0054278
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author Kobayashi, Tatsuya
Yan, Huimin
Kurahashi, Yasuhiro
Ito, Yuki
Maeda, Hiroshi
Tada, Tsuyoshi
Hongo, Kazuhiro
Nakayama, Jun
author_facet Kobayashi, Tatsuya
Yan, Huimin
Kurahashi, Yasuhiro
Ito, Yuki
Maeda, Hiroshi
Tada, Tsuyoshi
Hongo, Kazuhiro
Nakayama, Jun
author_sort Kobayashi, Tatsuya
collection PubMed
description N-Acetylgalactosamine 4-sulfate 6-O-sulfotransferase (GalNAc4S-6ST) is the sulfotransferase responsible for biosynthesis of highly sulfated chondroitin sulfate CS-E. Although involvements of CS-E in neuronal cell functions have been extensively analyzed, the role of GalNAc4S-6ST in astrocytic tumor progression remains unknown. Here, we reveal that GalNAc4S-6ST transcripts were detected in astrocytic tumors derived from all 30 patients examined using quantitative reverse transcription-PCR analysis. Patients with high GalNAc4S-6ST mRNA expression had significantly worse outcome compared with patients with low expression, and multivariate survival analysis disclosed that GalNAc4S-6ST is an independent poor prognostic factor for astrocytic tumors. We then tested whether CS-E enhanced haptotaxic migration of glioblastoma U251-MG cells that endogenously express both the CS-E’s scaffold tyrosine phosphatase ζ (PTPζ) and GalNAc4S-6ST, in the presence of CS-E’s preferred ligands, pleiotrophin (PTN) or midkine (MK), using a modified Boyden chamber method. Haptotaxic stimulation of cell migration by PTN was most robust on control siRNA-transfected U251-MG cells, while that enhancing effect was cancelled following transduction of GalNAc4S-6ST siRNA. Similar results were obtained using MK, suggesting that both PTN and MK enhance migration of U251-MG cells by binding to CS-E. We also found that PTPζ as well as PTN and MK were frequently expressed in astrocytic tumor cells. Thus, our findings indicate that GalNAc4S-6ST mRNA expressed by astrocytic tumor cells is associated with poor patient prognosis likely by enhancing CS-E-mediated tumor cell motility in the presence of PTN and/or MK.
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spelling pubmed-35478812013-01-24 Role of GalNAc4S-6ST in Astrocytic Tumor Progression Kobayashi, Tatsuya Yan, Huimin Kurahashi, Yasuhiro Ito, Yuki Maeda, Hiroshi Tada, Tsuyoshi Hongo, Kazuhiro Nakayama, Jun PLoS One Research Article N-Acetylgalactosamine 4-sulfate 6-O-sulfotransferase (GalNAc4S-6ST) is the sulfotransferase responsible for biosynthesis of highly sulfated chondroitin sulfate CS-E. Although involvements of CS-E in neuronal cell functions have been extensively analyzed, the role of GalNAc4S-6ST in astrocytic tumor progression remains unknown. Here, we reveal that GalNAc4S-6ST transcripts were detected in astrocytic tumors derived from all 30 patients examined using quantitative reverse transcription-PCR analysis. Patients with high GalNAc4S-6ST mRNA expression had significantly worse outcome compared with patients with low expression, and multivariate survival analysis disclosed that GalNAc4S-6ST is an independent poor prognostic factor for astrocytic tumors. We then tested whether CS-E enhanced haptotaxic migration of glioblastoma U251-MG cells that endogenously express both the CS-E’s scaffold tyrosine phosphatase ζ (PTPζ) and GalNAc4S-6ST, in the presence of CS-E’s preferred ligands, pleiotrophin (PTN) or midkine (MK), using a modified Boyden chamber method. Haptotaxic stimulation of cell migration by PTN was most robust on control siRNA-transfected U251-MG cells, while that enhancing effect was cancelled following transduction of GalNAc4S-6ST siRNA. Similar results were obtained using MK, suggesting that both PTN and MK enhance migration of U251-MG cells by binding to CS-E. We also found that PTPζ as well as PTN and MK were frequently expressed in astrocytic tumor cells. Thus, our findings indicate that GalNAc4S-6ST mRNA expressed by astrocytic tumor cells is associated with poor patient prognosis likely by enhancing CS-E-mediated tumor cell motility in the presence of PTN and/or MK. Public Library of Science 2013-01-17 /pmc/articles/PMC3547881/ /pubmed/23349846 http://dx.doi.org/10.1371/journal.pone.0054278 Text en © 2013 Kobayashi et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kobayashi, Tatsuya
Yan, Huimin
Kurahashi, Yasuhiro
Ito, Yuki
Maeda, Hiroshi
Tada, Tsuyoshi
Hongo, Kazuhiro
Nakayama, Jun
Role of GalNAc4S-6ST in Astrocytic Tumor Progression
title Role of GalNAc4S-6ST in Astrocytic Tumor Progression
title_full Role of GalNAc4S-6ST in Astrocytic Tumor Progression
title_fullStr Role of GalNAc4S-6ST in Astrocytic Tumor Progression
title_full_unstemmed Role of GalNAc4S-6ST in Astrocytic Tumor Progression
title_short Role of GalNAc4S-6ST in Astrocytic Tumor Progression
title_sort role of galnac4s-6st in astrocytic tumor progression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3547881/
https://www.ncbi.nlm.nih.gov/pubmed/23349846
http://dx.doi.org/10.1371/journal.pone.0054278
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