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Role of keratan sulfate expression in human pancreatic cancer malignancy
Keratan sulfate (KS) is a sulfated linear polymer of N-acetyllactosamine. Proteoglycans carrying keratan sulfate epitopes were majorly observed in cornea, cartilage and brain; and mainly involved in embryonic development, cornea transparency, and wound healing process. Recently, expression of KS in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609602/ https://www.ncbi.nlm.nih.gov/pubmed/31273306 http://dx.doi.org/10.1038/s41598-019-46046-6 |
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author | Leiphrakpam, Premila D. Patil, Prathamesh P. Remmers, Neeley Swanson, Benjamin Grandgenett, Paul M. Qiu, Fang Yu, Fang Radhakrishnan, Prakash |
author_facet | Leiphrakpam, Premila D. Patil, Prathamesh P. Remmers, Neeley Swanson, Benjamin Grandgenett, Paul M. Qiu, Fang Yu, Fang Radhakrishnan, Prakash |
author_sort | Leiphrakpam, Premila D. |
collection | PubMed |
description | Keratan sulfate (KS) is a sulfated linear polymer of N-acetyllactosamine. Proteoglycans carrying keratan sulfate epitopes were majorly observed in cornea, cartilage and brain; and mainly involved in embryonic development, cornea transparency, and wound healing process. Recently, expression of KS in cancer has been shown to be highly associated with advanced tumor grade and poor prognosis. Therefore, we aimed to identify the expression of KS epitope in human pancreatic cancer primary and metastatic tumor lesions. Immunohistochemical analysis of KS expression was performed on primary pancreatic tumors and metastatic tissues. We observed an increased expression of KS epitope on primary tumor tissues compared to uninvolved normal and tumor stroma; and is associated with worse overall survival. Moreover, lung metastatic tumors show a higher-level expression of KS compared to primary tumors. Interestingly, KS biosynthesis specific glycosyltransferases expression was differentially regulated in metastatic pancreatic tumors. Taken together, these results indicate that aberrant expression of KS is predictive of pancreatic cancer progression and metastasis and may serve as a novel prognostic biomarker for pancreatic cancer. |
format | Online Article Text |
id | pubmed-6609602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66096022019-07-14 Role of keratan sulfate expression in human pancreatic cancer malignancy Leiphrakpam, Premila D. Patil, Prathamesh P. Remmers, Neeley Swanson, Benjamin Grandgenett, Paul M. Qiu, Fang Yu, Fang Radhakrishnan, Prakash Sci Rep Article Keratan sulfate (KS) is a sulfated linear polymer of N-acetyllactosamine. Proteoglycans carrying keratan sulfate epitopes were majorly observed in cornea, cartilage and brain; and mainly involved in embryonic development, cornea transparency, and wound healing process. Recently, expression of KS in cancer has been shown to be highly associated with advanced tumor grade and poor prognosis. Therefore, we aimed to identify the expression of KS epitope in human pancreatic cancer primary and metastatic tumor lesions. Immunohistochemical analysis of KS expression was performed on primary pancreatic tumors and metastatic tissues. We observed an increased expression of KS epitope on primary tumor tissues compared to uninvolved normal and tumor stroma; and is associated with worse overall survival. Moreover, lung metastatic tumors show a higher-level expression of KS compared to primary tumors. Interestingly, KS biosynthesis specific glycosyltransferases expression was differentially regulated in metastatic pancreatic tumors. Taken together, these results indicate that aberrant expression of KS is predictive of pancreatic cancer progression and metastasis and may serve as a novel prognostic biomarker for pancreatic cancer. Nature Publishing Group UK 2019-07-04 /pmc/articles/PMC6609602/ /pubmed/31273306 http://dx.doi.org/10.1038/s41598-019-46046-6 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Leiphrakpam, Premila D. Patil, Prathamesh P. Remmers, Neeley Swanson, Benjamin Grandgenett, Paul M. Qiu, Fang Yu, Fang Radhakrishnan, Prakash Role of keratan sulfate expression in human pancreatic cancer malignancy |
title | Role of keratan sulfate expression in human pancreatic cancer malignancy |
title_full | Role of keratan sulfate expression in human pancreatic cancer malignancy |
title_fullStr | Role of keratan sulfate expression in human pancreatic cancer malignancy |
title_full_unstemmed | Role of keratan sulfate expression in human pancreatic cancer malignancy |
title_short | Role of keratan sulfate expression in human pancreatic cancer malignancy |
title_sort | role of keratan sulfate expression in human pancreatic cancer malignancy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609602/ https://www.ncbi.nlm.nih.gov/pubmed/31273306 http://dx.doi.org/10.1038/s41598-019-46046-6 |
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