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High expression of tissue O-linked glycans is associated with a malignant phenotype of cholangiocarcinoma

OBJECTIVE: This study aimed to investigate the expression of O-linked glycoprotein glycans in tissue of patients with cholangiocarcinoma compared with adjacent normal tissue. METHODS: Sixty patients with cholangiocarcinoma were included in the study. Permethylated O-linked glycans from intrahepatic...

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Autores principales: Talabnin, Krajang, Talabnin, Chutima, Khiaowichit, Juthamas, Sutatum, Nuchanard, Asavaritikrai, Pundit, Suksaweang, Sanong, Tongtawee, Taweesak, Ishihara, Mayumi, Azadi, Parastoo, Sripa, Banchob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869157/
https://www.ncbi.nlm.nih.gov/pubmed/33535865
http://dx.doi.org/10.1177/0300060520976864
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author Talabnin, Krajang
Talabnin, Chutima
Khiaowichit, Juthamas
Sutatum, Nuchanard
Asavaritikrai, Pundit
Suksaweang, Sanong
Tongtawee, Taweesak
Ishihara, Mayumi
Azadi, Parastoo
Sripa, Banchob
author_facet Talabnin, Krajang
Talabnin, Chutima
Khiaowichit, Juthamas
Sutatum, Nuchanard
Asavaritikrai, Pundit
Suksaweang, Sanong
Tongtawee, Taweesak
Ishihara, Mayumi
Azadi, Parastoo
Sripa, Banchob
author_sort Talabnin, Krajang
collection PubMed
description OBJECTIVE: This study aimed to investigate the expression of O-linked glycoprotein glycans in tissue of patients with cholangiocarcinoma compared with adjacent normal tissue. METHODS: Sixty patients with cholangiocarcinoma were included in the study. Permethylated O-linked glycans from intrahepatic cholangiocarcinoma tissue and adjacent normal tissue were analyzed using nano-spray ionization-linear ion trap mass spectrometry. Histochemistry of peanut agglutinin lectin was used for detection and localization of galactose (Gal) 1, N-acetyl-galactosamine (GalNAc) 1. RESULTS: O-linked glycans from patients with cholangiocarcinoma were composed of di- to hexa-saccharides with a terminal galactose and sialic acids (N-acetylneuraminic acid [NeuAc]). A total of eight O-linked glycan structures were detected. Gal1GalNAc1 and Gal2 N-acetyl-glucosamine 1 GalNAc1 expression was significantly higher in tissue from patients with cholangiocarcinoma compared with adjacent normal tissue, while NeuAc1Gal1GalNAc1 expression was significantly lower. High Gal1GalNAc1 expression was significantly associated with the late stage of cholangiocarcinoma (stages II–IV), lymphatic invasion, and vascular invasion. CONCLUSION: Our study shows expression of O-linked glycans in progression of cholangiocarcinoma and highlights the association of Gal1GalNAc1 with lymphatic and vascular invasion of cholangiocarcinoma.
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spelling pubmed-78691572021-02-19 High expression of tissue O-linked glycans is associated with a malignant phenotype of cholangiocarcinoma Talabnin, Krajang Talabnin, Chutima Khiaowichit, Juthamas Sutatum, Nuchanard Asavaritikrai, Pundit Suksaweang, Sanong Tongtawee, Taweesak Ishihara, Mayumi Azadi, Parastoo Sripa, Banchob J Int Med Res Pre-Clinical Research Report OBJECTIVE: This study aimed to investigate the expression of O-linked glycoprotein glycans in tissue of patients with cholangiocarcinoma compared with adjacent normal tissue. METHODS: Sixty patients with cholangiocarcinoma were included in the study. Permethylated O-linked glycans from intrahepatic cholangiocarcinoma tissue and adjacent normal tissue were analyzed using nano-spray ionization-linear ion trap mass spectrometry. Histochemistry of peanut agglutinin lectin was used for detection and localization of galactose (Gal) 1, N-acetyl-galactosamine (GalNAc) 1. RESULTS: O-linked glycans from patients with cholangiocarcinoma were composed of di- to hexa-saccharides with a terminal galactose and sialic acids (N-acetylneuraminic acid [NeuAc]). A total of eight O-linked glycan structures were detected. Gal1GalNAc1 and Gal2 N-acetyl-glucosamine 1 GalNAc1 expression was significantly higher in tissue from patients with cholangiocarcinoma compared with adjacent normal tissue, while NeuAc1Gal1GalNAc1 expression was significantly lower. High Gal1GalNAc1 expression was significantly associated with the late stage of cholangiocarcinoma (stages II–IV), lymphatic invasion, and vascular invasion. CONCLUSION: Our study shows expression of O-linked glycans in progression of cholangiocarcinoma and highlights the association of Gal1GalNAc1 with lymphatic and vascular invasion of cholangiocarcinoma. SAGE Publications 2021-02-04 /pmc/articles/PMC7869157/ /pubmed/33535865 http://dx.doi.org/10.1177/0300060520976864 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Pre-Clinical Research Report
Talabnin, Krajang
Talabnin, Chutima
Khiaowichit, Juthamas
Sutatum, Nuchanard
Asavaritikrai, Pundit
Suksaweang, Sanong
Tongtawee, Taweesak
Ishihara, Mayumi
Azadi, Parastoo
Sripa, Banchob
High expression of tissue O-linked glycans is associated with a malignant phenotype of cholangiocarcinoma
title High expression of tissue O-linked glycans is associated with a malignant phenotype of cholangiocarcinoma
title_full High expression of tissue O-linked glycans is associated with a malignant phenotype of cholangiocarcinoma
title_fullStr High expression of tissue O-linked glycans is associated with a malignant phenotype of cholangiocarcinoma
title_full_unstemmed High expression of tissue O-linked glycans is associated with a malignant phenotype of cholangiocarcinoma
title_short High expression of tissue O-linked glycans is associated with a malignant phenotype of cholangiocarcinoma
title_sort high expression of tissue o-linked glycans is associated with a malignant phenotype of cholangiocarcinoma
topic Pre-Clinical Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869157/
https://www.ncbi.nlm.nih.gov/pubmed/33535865
http://dx.doi.org/10.1177/0300060520976864
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