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Serum endostatin levels are elevated in colorectal cancer and correlate with invasion and systemic inflammatory markers

BACKGROUND: Endostatin, a fragment of collagen XVIII, is an endogenous angiogenesis inhibitor with anti-tumour functions. However, elevated circulating endostatin concentrations have been found in several human cancers including colorectal cancer (CRC). METHODS: Serum endostatin levels were measured...

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Autores principales: Kantola, T, Väyrynen, J P, Klintrup, K, Mäkelä, J, Karppinen, S M, Pihlajaniemi, T, Autio-Harmainen, H, Karttunen, T J, Mäkinen, M J, Tuomisto, A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4200096/
https://www.ncbi.nlm.nih.gov/pubmed/25137019
http://dx.doi.org/10.1038/bjc.2014.456
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author Kantola, T
Väyrynen, J P
Klintrup, K
Mäkelä, J
Karppinen, S M
Pihlajaniemi, T
Autio-Harmainen, H
Karttunen, T J
Mäkinen, M J
Tuomisto, A
author_facet Kantola, T
Väyrynen, J P
Klintrup, K
Mäkelä, J
Karppinen, S M
Pihlajaniemi, T
Autio-Harmainen, H
Karttunen, T J
Mäkinen, M J
Tuomisto, A
author_sort Kantola, T
collection PubMed
description BACKGROUND: Endostatin, a fragment of collagen XVIII, is an endogenous angiogenesis inhibitor with anti-tumour functions. However, elevated circulating endostatin concentrations have been found in several human cancers including colorectal cancer (CRC). METHODS: Serum endostatin levels were measured by enzyme-linked immunoassay from a series of 143 patients with CRC and from 84 controls, and correlated with detailed clinicopathological features of CRC, serum leukocyte differential count and C-reactive protein (CRP) levels. RESULTS: Patients with CRC had higher serum endostatin levels than the controls (P=0.005), and high levels associated with age, tumour invasion through the muscularis propria and poor differentiation, but not with metastases. Endostatin levels showed a positive correlation with the markers of systemic inflammatory response and a negative correlation with the densities of tumour-infiltrating mast cells and dendritic cells. Collagen XVIII was expressed in tumour stroma most strikingly in blood vessels and capillaries, and in the muscle layer of the bowel wall. CONCLUSIONS: Elevated endostatin levels in CRC correlate with systemic inflammation and invasion through the muscularis propria. Increased endostatin level may be a result of invasion-related cleavage of collagen XVIII expressed in the bowel wall. The negative correlations between serum endostatin and intratumoural mast cells and immature dendritic cells may reflect angiogenesis inhibition by endostatin.
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spelling pubmed-42000962015-10-14 Serum endostatin levels are elevated in colorectal cancer and correlate with invasion and systemic inflammatory markers Kantola, T Väyrynen, J P Klintrup, K Mäkelä, J Karppinen, S M Pihlajaniemi, T Autio-Harmainen, H Karttunen, T J Mäkinen, M J Tuomisto, A Br J Cancer Molecular Diagnostics BACKGROUND: Endostatin, a fragment of collagen XVIII, is an endogenous angiogenesis inhibitor with anti-tumour functions. However, elevated circulating endostatin concentrations have been found in several human cancers including colorectal cancer (CRC). METHODS: Serum endostatin levels were measured by enzyme-linked immunoassay from a series of 143 patients with CRC and from 84 controls, and correlated with detailed clinicopathological features of CRC, serum leukocyte differential count and C-reactive protein (CRP) levels. RESULTS: Patients with CRC had higher serum endostatin levels than the controls (P=0.005), and high levels associated with age, tumour invasion through the muscularis propria and poor differentiation, but not with metastases. Endostatin levels showed a positive correlation with the markers of systemic inflammatory response and a negative correlation with the densities of tumour-infiltrating mast cells and dendritic cells. Collagen XVIII was expressed in tumour stroma most strikingly in blood vessels and capillaries, and in the muscle layer of the bowel wall. CONCLUSIONS: Elevated endostatin levels in CRC correlate with systemic inflammation and invasion through the muscularis propria. Increased endostatin level may be a result of invasion-related cleavage of collagen XVIII expressed in the bowel wall. The negative correlations between serum endostatin and intratumoural mast cells and immature dendritic cells may reflect angiogenesis inhibition by endostatin. Nature Publishing Group 2014-10-14 2014-08-19 /pmc/articles/PMC4200096/ /pubmed/25137019 http://dx.doi.org/10.1038/bjc.2014.456 Text en Copyright © 2014 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Molecular Diagnostics
Kantola, T
Väyrynen, J P
Klintrup, K
Mäkelä, J
Karppinen, S M
Pihlajaniemi, T
Autio-Harmainen, H
Karttunen, T J
Mäkinen, M J
Tuomisto, A
Serum endostatin levels are elevated in colorectal cancer and correlate with invasion and systemic inflammatory markers
title Serum endostatin levels are elevated in colorectal cancer and correlate with invasion and systemic inflammatory markers
title_full Serum endostatin levels are elevated in colorectal cancer and correlate with invasion and systemic inflammatory markers
title_fullStr Serum endostatin levels are elevated in colorectal cancer and correlate with invasion and systemic inflammatory markers
title_full_unstemmed Serum endostatin levels are elevated in colorectal cancer and correlate with invasion and systemic inflammatory markers
title_short Serum endostatin levels are elevated in colorectal cancer and correlate with invasion and systemic inflammatory markers
title_sort serum endostatin levels are elevated in colorectal cancer and correlate with invasion and systemic inflammatory markers
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4200096/
https://www.ncbi.nlm.nih.gov/pubmed/25137019
http://dx.doi.org/10.1038/bjc.2014.456
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