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Expression and localisation of MUC1 modified with sialylated core-2 O-glycans in mucoepidermoid carcinoma

Mucoepidermoid carcinoma (MEC) is the most frequent of the rare salivary gland malignancies. We previously reported high expression of Mucin 1 (MUC1) modified with sialylated core-2 O-glycans in MEC by using tissue homogenates. In this study, we characterised glycan structures of MEC and identified...

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Autores principales: Sugiura, Takanori, Hashimoto, Kazuhiko, Kikuta, Kazutaka, Anazawa, Ukei, Nomura, Takeshi, Kameyama, Akihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082819/
https://www.ncbi.nlm.nih.gov/pubmed/37031283
http://dx.doi.org/10.1038/s41598-023-32597-2
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author Sugiura, Takanori
Hashimoto, Kazuhiko
Kikuta, Kazutaka
Anazawa, Ukei
Nomura, Takeshi
Kameyama, Akihiko
author_facet Sugiura, Takanori
Hashimoto, Kazuhiko
Kikuta, Kazutaka
Anazawa, Ukei
Nomura, Takeshi
Kameyama, Akihiko
author_sort Sugiura, Takanori
collection PubMed
description Mucoepidermoid carcinoma (MEC) is the most frequent of the rare salivary gland malignancies. We previously reported high expression of Mucin 1 (MUC1) modified with sialylated core-2 O-glycans in MEC by using tissue homogenates. In this study, we characterised glycan structures of MEC and identified the localisation of cells expressing these distinctive glycans on MUC1. Mucins were extracted from the frozen tissues of three patients with MEC, and normal salivary glands (NSGs) extracted from seven patients, separated by supported molecular matrix electrophoresis (SMME) and the membranes stained with various lectins. In addition, formalin-fixed, paraffin-embedded sections from three patients with MEC were subjected to immunohistochemistry (IHC) with various monoclonal antibodies and analysed for C2GnT-1 expression by in situ hybridisation (ISH). Lectin blotting of the SMME membranes revealed that glycans on MUC1 from MEC samples contained α2,3-linked sialic acid. In IHC, MUC1 was diffusely detected at MEC-affected regions but was specifically detected at apical membranes in NSGs. ISH showed that C2GnT-1 was expressed at the MUC1-positive in MEC-affected regions but not in the NSG. MEC cells produced MUC1 modified with α2,3-linked sialic acid-containing core-2 O-glycans. MUC1 containing these glycans deserves further study as a new potential diagnostic marker of MEC.
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spelling pubmed-100828192023-04-10 Expression and localisation of MUC1 modified with sialylated core-2 O-glycans in mucoepidermoid carcinoma Sugiura, Takanori Hashimoto, Kazuhiko Kikuta, Kazutaka Anazawa, Ukei Nomura, Takeshi Kameyama, Akihiko Sci Rep Article Mucoepidermoid carcinoma (MEC) is the most frequent of the rare salivary gland malignancies. We previously reported high expression of Mucin 1 (MUC1) modified with sialylated core-2 O-glycans in MEC by using tissue homogenates. In this study, we characterised glycan structures of MEC and identified the localisation of cells expressing these distinctive glycans on MUC1. Mucins were extracted from the frozen tissues of three patients with MEC, and normal salivary glands (NSGs) extracted from seven patients, separated by supported molecular matrix electrophoresis (SMME) and the membranes stained with various lectins. In addition, formalin-fixed, paraffin-embedded sections from three patients with MEC were subjected to immunohistochemistry (IHC) with various monoclonal antibodies and analysed for C2GnT-1 expression by in situ hybridisation (ISH). Lectin blotting of the SMME membranes revealed that glycans on MUC1 from MEC samples contained α2,3-linked sialic acid. In IHC, MUC1 was diffusely detected at MEC-affected regions but was specifically detected at apical membranes in NSGs. ISH showed that C2GnT-1 was expressed at the MUC1-positive in MEC-affected regions but not in the NSG. MEC cells produced MUC1 modified with α2,3-linked sialic acid-containing core-2 O-glycans. MUC1 containing these glycans deserves further study as a new potential diagnostic marker of MEC. Nature Publishing Group UK 2023-04-08 /pmc/articles/PMC10082819/ /pubmed/37031283 http://dx.doi.org/10.1038/s41598-023-32597-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Sugiura, Takanori
Hashimoto, Kazuhiko
Kikuta, Kazutaka
Anazawa, Ukei
Nomura, Takeshi
Kameyama, Akihiko
Expression and localisation of MUC1 modified with sialylated core-2 O-glycans in mucoepidermoid carcinoma
title Expression and localisation of MUC1 modified with sialylated core-2 O-glycans in mucoepidermoid carcinoma
title_full Expression and localisation of MUC1 modified with sialylated core-2 O-glycans in mucoepidermoid carcinoma
title_fullStr Expression and localisation of MUC1 modified with sialylated core-2 O-glycans in mucoepidermoid carcinoma
title_full_unstemmed Expression and localisation of MUC1 modified with sialylated core-2 O-glycans in mucoepidermoid carcinoma
title_short Expression and localisation of MUC1 modified with sialylated core-2 O-glycans in mucoepidermoid carcinoma
title_sort expression and localisation of muc1 modified with sialylated core-2 o-glycans in mucoepidermoid carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10082819/
https://www.ncbi.nlm.nih.gov/pubmed/37031283
http://dx.doi.org/10.1038/s41598-023-32597-2
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