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The Utility of Formalin-fixed and Paraffin-embedded Tissue Blocks for Quantitative Analysis of N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase mRNA Expressed by Colorectal Cancer Cells

N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase (GalNAc4S-6ST) is a sulfotransferase responsible for biosynthesis of chondroitin sulfate E (CS-E). CS-E plays important roles in numerous biological events, such as neurite outgrowth. However, the role of GalNAc4S-6ST in tumor progression remains...

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Detalles Bibliográficos
Autores principales: Ito, Yuki, Watanabe, Matsuko, Nishizawa, Tomoko, Omachi, Toshiya, Kobayashi, Tatsuya, Kasama, Susumu, Habuchi, Osami, Nakayama, Jun
Formato: Texto
Lenguaje:English
Publicado: Japan Society of Histochemistry and Cytochemistry 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1874510/
https://www.ncbi.nlm.nih.gov/pubmed/17576433
http://dx.doi.org/10.1267/ahc.07004
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author Ito, Yuki
Watanabe, Matsuko
Nishizawa, Tomoko
Omachi, Toshiya
Kobayashi, Tatsuya
Kasama, Susumu
Habuchi, Osami
Nakayama, Jun
author_facet Ito, Yuki
Watanabe, Matsuko
Nishizawa, Tomoko
Omachi, Toshiya
Kobayashi, Tatsuya
Kasama, Susumu
Habuchi, Osami
Nakayama, Jun
author_sort Ito, Yuki
collection PubMed
description N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase (GalNAc4S-6ST) is a sulfotransferase responsible for biosynthesis of chondroitin sulfate E (CS-E). CS-E plays important roles in numerous biological events, such as neurite outgrowth. However, the role of GalNAc4S-6ST in tumor progression remains unknown. In the present study, we analyzed expression of GalNAc4S-6ST mRNA in colorectal cancer by combining real-time RT-PCR with in situ hybridization (ISH) using archived formalin-fixed and paraffin-embedded tissue sections. In 57.5% of 40 patients, expression of GalNAc4S-6ST mRNA was increased in cancer tissues compared with paired normal mucosa. ISH using an RNA probe specific for GalNAc4S-6ST revealed that it was expressed in colorectal cancer cells. Analysis of the relationship between expression of GalNAc4S-6ST as determined by real-time RT-PCR assay and various clinicopathological variables revealed that GalNAc4S-6ST was associated with vessel invasion, although a statistically significant difference was not seen (P=0.125 for lymphatic vessel invasion and P=0.242 for venous invasion). Taken together, we show that real-time RT-PCR combined with ISH is useful to investigate quantitatively GalNAc4S-6ST mRNA expression in formalin-fixed and paraffin-embedded tissue sections, and that GalNAc4S-6ST expressed by colorectal cancer cells plays a minor role in tumor progression.
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spelling pubmed-18745102007-06-18 The Utility of Formalin-fixed and Paraffin-embedded Tissue Blocks for Quantitative Analysis of N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase mRNA Expressed by Colorectal Cancer Cells Ito, Yuki Watanabe, Matsuko Nishizawa, Tomoko Omachi, Toshiya Kobayashi, Tatsuya Kasama, Susumu Habuchi, Osami Nakayama, Jun Acta Histochem Cytochem Regular Article N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase (GalNAc4S-6ST) is a sulfotransferase responsible for biosynthesis of chondroitin sulfate E (CS-E). CS-E plays important roles in numerous biological events, such as neurite outgrowth. However, the role of GalNAc4S-6ST in tumor progression remains unknown. In the present study, we analyzed expression of GalNAc4S-6ST mRNA in colorectal cancer by combining real-time RT-PCR with in situ hybridization (ISH) using archived formalin-fixed and paraffin-embedded tissue sections. In 57.5% of 40 patients, expression of GalNAc4S-6ST mRNA was increased in cancer tissues compared with paired normal mucosa. ISH using an RNA probe specific for GalNAc4S-6ST revealed that it was expressed in colorectal cancer cells. Analysis of the relationship between expression of GalNAc4S-6ST as determined by real-time RT-PCR assay and various clinicopathological variables revealed that GalNAc4S-6ST was associated with vessel invasion, although a statistically significant difference was not seen (P=0.125 for lymphatic vessel invasion and P=0.242 for venous invasion). Taken together, we show that real-time RT-PCR combined with ISH is useful to investigate quantitatively GalNAc4S-6ST mRNA expression in formalin-fixed and paraffin-embedded tissue sections, and that GalNAc4S-6ST expressed by colorectal cancer cells plays a minor role in tumor progression. Japan Society of Histochemistry and Cytochemistry 2007-05-12 2007-05-10 /pmc/articles/PMC1874510/ /pubmed/17576433 http://dx.doi.org/10.1267/ahc.07004 Text en Copyright © 2007 AHC
spellingShingle Regular Article
Ito, Yuki
Watanabe, Matsuko
Nishizawa, Tomoko
Omachi, Toshiya
Kobayashi, Tatsuya
Kasama, Susumu
Habuchi, Osami
Nakayama, Jun
The Utility of Formalin-fixed and Paraffin-embedded Tissue Blocks for Quantitative Analysis of N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase mRNA Expressed by Colorectal Cancer Cells
title The Utility of Formalin-fixed and Paraffin-embedded Tissue Blocks for Quantitative Analysis of N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase mRNA Expressed by Colorectal Cancer Cells
title_full The Utility of Formalin-fixed and Paraffin-embedded Tissue Blocks for Quantitative Analysis of N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase mRNA Expressed by Colorectal Cancer Cells
title_fullStr The Utility of Formalin-fixed and Paraffin-embedded Tissue Blocks for Quantitative Analysis of N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase mRNA Expressed by Colorectal Cancer Cells
title_full_unstemmed The Utility of Formalin-fixed and Paraffin-embedded Tissue Blocks for Quantitative Analysis of N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase mRNA Expressed by Colorectal Cancer Cells
title_short The Utility of Formalin-fixed and Paraffin-embedded Tissue Blocks for Quantitative Analysis of N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase mRNA Expressed by Colorectal Cancer Cells
title_sort utility of formalin-fixed and paraffin-embedded tissue blocks for quantitative analysis of n-acetylgalactosamine 4-sulfate 6-o-sulfotransferase mrna expressed by colorectal cancer cells
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1874510/
https://www.ncbi.nlm.nih.gov/pubmed/17576433
http://dx.doi.org/10.1267/ahc.07004
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