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Characterization of tumor-associated MUC1 and its glycans expressed in mucoepidermoid carcinoma

Mucoepidermoid carcinoma (MEC) is one of the most frequently misdiagnosed tumors. Glycans are modulated by malignant transformation. Mucin 1 (MUC1) is a mucin whose expression is upregulated in various tumors, including MEC, and it has previously been investigated as a diagnostic and prognostic tumo...

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Autores principales: Isaka, Eisaku, Sugiura, Takanori, Hashimoto, Kazuhiko, Kikuta, Kazutaka, Anazawa, Ukei, Nomura, Takeshi, Kameyama, Akihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358622/
https://www.ncbi.nlm.nih.gov/pubmed/34457057
http://dx.doi.org/10.3892/ol.2021.12963
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author Isaka, Eisaku
Sugiura, Takanori
Hashimoto, Kazuhiko
Kikuta, Kazutaka
Anazawa, Ukei
Nomura, Takeshi
Kameyama, Akihiko
author_facet Isaka, Eisaku
Sugiura, Takanori
Hashimoto, Kazuhiko
Kikuta, Kazutaka
Anazawa, Ukei
Nomura, Takeshi
Kameyama, Akihiko
author_sort Isaka, Eisaku
collection PubMed
description Mucoepidermoid carcinoma (MEC) is one of the most frequently misdiagnosed tumors. Glycans are modulated by malignant transformation. Mucin 1 (MUC1) is a mucin whose expression is upregulated in various tumors, including MEC, and it has previously been investigated as a diagnostic and prognostic tumor marker. The present study aimed to reveal the differences in the mucin glycans between MEC and normal salivary glands (NSGs) to discover novel diagnostic markers. Soluble fractions of salivary gland homogenate prepared from three MEC salivary glands and 7 NSGs were evaluated. Mucins in MEC and NSGs were separated using supported molecular matrix electrophoresis, and stained with Alcian blue and monoclonal antibodies. The glycans of the separated mucins were analyzed by mass spectrometry. MUC1 was found in MEC but not in NSGs, and almost all glycans of MUC1 in MEC were sialylated, whereas the glycans of mucins in NSGs were less sialylated. The core 2 type glycans, (Hex)(2)(HexNAc)(2)(NeuAc)(1) and (Hex)(2)(HexNAc)(2)(NeuAc)(2), were found to be significantly abundant glycans of MUC1 in MEC. MEC markedly produced MUC1 modified with sialylated core 2 glycans. These data were obtained from the soluble fractions of salivary gland homogenates. These findings provide a basis for the utilization of MUC1 as a serum diagnostic marker for the preoperative diagnosis of MEC.
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spelling pubmed-83586222021-08-26 Characterization of tumor-associated MUC1 and its glycans expressed in mucoepidermoid carcinoma Isaka, Eisaku Sugiura, Takanori Hashimoto, Kazuhiko Kikuta, Kazutaka Anazawa, Ukei Nomura, Takeshi Kameyama, Akihiko Oncol Lett Articles Mucoepidermoid carcinoma (MEC) is one of the most frequently misdiagnosed tumors. Glycans are modulated by malignant transformation. Mucin 1 (MUC1) is a mucin whose expression is upregulated in various tumors, including MEC, and it has previously been investigated as a diagnostic and prognostic tumor marker. The present study aimed to reveal the differences in the mucin glycans between MEC and normal salivary glands (NSGs) to discover novel diagnostic markers. Soluble fractions of salivary gland homogenate prepared from three MEC salivary glands and 7 NSGs were evaluated. Mucins in MEC and NSGs were separated using supported molecular matrix electrophoresis, and stained with Alcian blue and monoclonal antibodies. The glycans of the separated mucins were analyzed by mass spectrometry. MUC1 was found in MEC but not in NSGs, and almost all glycans of MUC1 in MEC were sialylated, whereas the glycans of mucins in NSGs were less sialylated. The core 2 type glycans, (Hex)(2)(HexNAc)(2)(NeuAc)(1) and (Hex)(2)(HexNAc)(2)(NeuAc)(2), were found to be significantly abundant glycans of MUC1 in MEC. MEC markedly produced MUC1 modified with sialylated core 2 glycans. These data were obtained from the soluble fractions of salivary gland homogenates. These findings provide a basis for the utilization of MUC1 as a serum diagnostic marker for the preoperative diagnosis of MEC. D.A. Spandidos 2021-10 2021-08-03 /pmc/articles/PMC8358622/ /pubmed/34457057 http://dx.doi.org/10.3892/ol.2021.12963 Text en Copyright: © Isaka et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Isaka, Eisaku
Sugiura, Takanori
Hashimoto, Kazuhiko
Kikuta, Kazutaka
Anazawa, Ukei
Nomura, Takeshi
Kameyama, Akihiko
Characterization of tumor-associated MUC1 and its glycans expressed in mucoepidermoid carcinoma
title Characterization of tumor-associated MUC1 and its glycans expressed in mucoepidermoid carcinoma
title_full Characterization of tumor-associated MUC1 and its glycans expressed in mucoepidermoid carcinoma
title_fullStr Characterization of tumor-associated MUC1 and its glycans expressed in mucoepidermoid carcinoma
title_full_unstemmed Characterization of tumor-associated MUC1 and its glycans expressed in mucoepidermoid carcinoma
title_short Characterization of tumor-associated MUC1 and its glycans expressed in mucoepidermoid carcinoma
title_sort characterization of tumor-associated muc1 and its glycans expressed in mucoepidermoid carcinoma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358622/
https://www.ncbi.nlm.nih.gov/pubmed/34457057
http://dx.doi.org/10.3892/ol.2021.12963
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