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Type IV collagen is a tumour stroma-derived biomarker for pancreas cancer

BACKGROUND: Pancreas cancer is a dreaded disease with high mortality, despite progress in surgical and oncological treatments in recent years. The field is hampered by a lack of good prognostic and predictive tumour biomarkers to be used during follow-up of patients. METHODS: The circulating level o...

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Autores principales: Öhlund, D, Lundin, C, Ardnor, B, Öman, M, Naredi, P, Sund, M
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2713699/
https://www.ncbi.nlm.nih.gov/pubmed/19491897
http://dx.doi.org/10.1038/sj.bjc.6605107
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author Öhlund, D
Lundin, C
Ardnor, B
Öman, M
Naredi, P
Sund, M
author_facet Öhlund, D
Lundin, C
Ardnor, B
Öman, M
Naredi, P
Sund, M
author_sort Öhlund, D
collection PubMed
description BACKGROUND: Pancreas cancer is a dreaded disease with high mortality, despite progress in surgical and oncological treatments in recent years. The field is hampered by a lack of good prognostic and predictive tumour biomarkers to be used during follow-up of patients. METHODS: The circulating level of type IV collagen was measured by ELISA in pancreas cancer patients and controls. The expression pattern of type IV collagen in normal pancreas, pancreas cancer tissue and in pancreas cancer cell lines was studied by immunofluorescence and Western blot techniques. RESULTS: Patients with pancreas cancer have significantly increased circulating levels of type IV collagen. In pancreas cancer tissue high levels of type IV collagen expression was found in close proximity to cancer cells in the tumour stroma. Furthermore, pancreas cancer cells were found to produce and secrete type IV collagen in vitro, which in part can explain the high type IV collagen expression observed in pancreas cancer tissue, and the increased circulating levels in pancreas cancer patients. Of clinical importance, our results show that the circulating level of type IV collagen after surgery is strongly related to prognosis in patients treated for pancreas cancer by pancreatico-duodenectomy with curative intent. Persisting high levels of circulating type IV collagen after surgery indicates a quick relapse in disease and poor survival. CONCLUSION: Our results most importantly show that stroma related substances can be evaluated as potential cancer biomarkers, and thereby underline the importance of the tumour microenvironment also in this context.
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spelling pubmed-27136992010-07-07 Type IV collagen is a tumour stroma-derived biomarker for pancreas cancer Öhlund, D Lundin, C Ardnor, B Öman, M Naredi, P Sund, M Br J Cancer Molecular Diagnostics BACKGROUND: Pancreas cancer is a dreaded disease with high mortality, despite progress in surgical and oncological treatments in recent years. The field is hampered by a lack of good prognostic and predictive tumour biomarkers to be used during follow-up of patients. METHODS: The circulating level of type IV collagen was measured by ELISA in pancreas cancer patients and controls. The expression pattern of type IV collagen in normal pancreas, pancreas cancer tissue and in pancreas cancer cell lines was studied by immunofluorescence and Western blot techniques. RESULTS: Patients with pancreas cancer have significantly increased circulating levels of type IV collagen. In pancreas cancer tissue high levels of type IV collagen expression was found in close proximity to cancer cells in the tumour stroma. Furthermore, pancreas cancer cells were found to produce and secrete type IV collagen in vitro, which in part can explain the high type IV collagen expression observed in pancreas cancer tissue, and the increased circulating levels in pancreas cancer patients. Of clinical importance, our results show that the circulating level of type IV collagen after surgery is strongly related to prognosis in patients treated for pancreas cancer by pancreatico-duodenectomy with curative intent. Persisting high levels of circulating type IV collagen after surgery indicates a quick relapse in disease and poor survival. CONCLUSION: Our results most importantly show that stroma related substances can be evaluated as potential cancer biomarkers, and thereby underline the importance of the tumour microenvironment also in this context. Nature Publishing Group 2009-07-07 2009-06-02 /pmc/articles/PMC2713699/ /pubmed/19491897 http://dx.doi.org/10.1038/sj.bjc.6605107 Text en Copyright © 2009 Cancer Research UK https://creativecommons.org/licenses/by/4.0/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 https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular Diagnostics
Öhlund, D
Lundin, C
Ardnor, B
Öman, M
Naredi, P
Sund, M
Type IV collagen is a tumour stroma-derived biomarker for pancreas cancer
title Type IV collagen is a tumour stroma-derived biomarker for pancreas cancer
title_full Type IV collagen is a tumour stroma-derived biomarker for pancreas cancer
title_fullStr Type IV collagen is a tumour stroma-derived biomarker for pancreas cancer
title_full_unstemmed Type IV collagen is a tumour stroma-derived biomarker for pancreas cancer
title_short Type IV collagen is a tumour stroma-derived biomarker for pancreas cancer
title_sort type iv collagen is a tumour stroma-derived biomarker for pancreas cancer
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2713699/
https://www.ncbi.nlm.nih.gov/pubmed/19491897
http://dx.doi.org/10.1038/sj.bjc.6605107
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