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High-serum MMP-8 levels are associated with decreased survival and systemic inflammation in colorectal cancer

BACKGROUND: Matrix metalloproteinase-8 (MMP-8) is a protease mainly expressed by neutrophils that cleaves numerous substrates, including collagens and cytokines. We have previously shown that serum MMP-8 levels increase in colorectal cancer (CRC) and correlate with distant metastasis. However, short...

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Autores principales: Sirniö, Päivi, Tuomisto, Anne, Tervahartiala, Taina, Sorsa, Timo, Klintrup, Kai, Karhu, Toni, Herzig, Karl-Heinz, Mäkelä, Jyrki, Karttunen, Tuomo J., Salo, Tuula, Mäkinen, Markus J., Väyrynen, Juha P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048114/
https://www.ncbi.nlm.nih.gov/pubmed/29808017
http://dx.doi.org/10.1038/s41416-018-0136-4
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author Sirniö, Päivi
Tuomisto, Anne
Tervahartiala, Taina
Sorsa, Timo
Klintrup, Kai
Karhu, Toni
Herzig, Karl-Heinz
Mäkelä, Jyrki
Karttunen, Tuomo J.
Salo, Tuula
Mäkinen, Markus J.
Väyrynen, Juha P.
author_facet Sirniö, Päivi
Tuomisto, Anne
Tervahartiala, Taina
Sorsa, Timo
Klintrup, Kai
Karhu, Toni
Herzig, Karl-Heinz
Mäkelä, Jyrki
Karttunen, Tuomo J.
Salo, Tuula
Mäkinen, Markus J.
Väyrynen, Juha P.
author_sort Sirniö, Päivi
collection PubMed
description BACKGROUND: Matrix metalloproteinase-8 (MMP-8) is a protease mainly expressed by neutrophils that cleaves numerous substrates, including collagens and cytokines. We have previously shown that serum MMP-8 levels increase in colorectal cancer (CRC) and correlate with distant metastasis. However, short follow-up in our prospective cohort did not enable survival analyses at the time of the first publication. METHODS: Preoperative serum MMP-8 levels were measured by immunofluorometric assay in 271 CRC patients and related to clinicopathological parameters, markers of systemic inflammation (modified Glasgow Prognostic Score, mGPS; serum levels of C-reactive protein (CRP), albumin and 13 cytokines), the density of six types of tumour-infiltrating immune cells and survival. RESULTS: Increased MMP-8 levels associated with higher mGPS and higher serum levels of CRP and several cytokines, including IL-1ra, IL-7 and IL-8 (p < 0.001 for all). Serum MMP-8 negatively correlated with tumour-infiltrating mast cells (invasive margin: p = 0.005, tumour centre: p = 0.010). The patients with high-serum MMP-8 levels (>100 ng/mL) had poor cancer-specific survival, independent of tumour stage, grade, lymphatic invasion, patient age, BRAF VE1 immunohistochemistry, mismatch repair deficiency, Immunoscore and mGPS (multivariate HR 2.12, 95% CI 1.21–3.71, p = 0.009). CONCLUSIONS: High-serum MMP-8 levels are associated with systemic inflammation and adverse outcome in CRC.
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spelling pubmed-60481142019-07-17 High-serum MMP-8 levels are associated with decreased survival and systemic inflammation in colorectal cancer Sirniö, Päivi Tuomisto, Anne Tervahartiala, Taina Sorsa, Timo Klintrup, Kai Karhu, Toni Herzig, Karl-Heinz Mäkelä, Jyrki Karttunen, Tuomo J. Salo, Tuula Mäkinen, Markus J. Väyrynen, Juha P. Br J Cancer Article BACKGROUND: Matrix metalloproteinase-8 (MMP-8) is a protease mainly expressed by neutrophils that cleaves numerous substrates, including collagens and cytokines. We have previously shown that serum MMP-8 levels increase in colorectal cancer (CRC) and correlate with distant metastasis. However, short follow-up in our prospective cohort did not enable survival analyses at the time of the first publication. METHODS: Preoperative serum MMP-8 levels were measured by immunofluorometric assay in 271 CRC patients and related to clinicopathological parameters, markers of systemic inflammation (modified Glasgow Prognostic Score, mGPS; serum levels of C-reactive protein (CRP), albumin and 13 cytokines), the density of six types of tumour-infiltrating immune cells and survival. RESULTS: Increased MMP-8 levels associated with higher mGPS and higher serum levels of CRP and several cytokines, including IL-1ra, IL-7 and IL-8 (p < 0.001 for all). Serum MMP-8 negatively correlated with tumour-infiltrating mast cells (invasive margin: p = 0.005, tumour centre: p = 0.010). The patients with high-serum MMP-8 levels (>100 ng/mL) had poor cancer-specific survival, independent of tumour stage, grade, lymphatic invasion, patient age, BRAF VE1 immunohistochemistry, mismatch repair deficiency, Immunoscore and mGPS (multivariate HR 2.12, 95% CI 1.21–3.71, p = 0.009). CONCLUSIONS: High-serum MMP-8 levels are associated with systemic inflammation and adverse outcome in CRC. Nature Publishing Group UK 2018-05-29 2018-07-17 /pmc/articles/PMC6048114/ /pubmed/29808017 http://dx.doi.org/10.1038/s41416-018-0136-4 Text en © Cancer Research UK 2018 https://creativecommons.org/licenses/by/4.0/Note: This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution 4.0 International (CC BY 4.0).
spellingShingle Article
Sirniö, Päivi
Tuomisto, Anne
Tervahartiala, Taina
Sorsa, Timo
Klintrup, Kai
Karhu, Toni
Herzig, Karl-Heinz
Mäkelä, Jyrki
Karttunen, Tuomo J.
Salo, Tuula
Mäkinen, Markus J.
Väyrynen, Juha P.
High-serum MMP-8 levels are associated with decreased survival and systemic inflammation in colorectal cancer
title High-serum MMP-8 levels are associated with decreased survival and systemic inflammation in colorectal cancer
title_full High-serum MMP-8 levels are associated with decreased survival and systemic inflammation in colorectal cancer
title_fullStr High-serum MMP-8 levels are associated with decreased survival and systemic inflammation in colorectal cancer
title_full_unstemmed High-serum MMP-8 levels are associated with decreased survival and systemic inflammation in colorectal cancer
title_short High-serum MMP-8 levels are associated with decreased survival and systemic inflammation in colorectal cancer
title_sort high-serum mmp-8 levels are associated with decreased survival and systemic inflammation in colorectal cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6048114/
https://www.ncbi.nlm.nih.gov/pubmed/29808017
http://dx.doi.org/10.1038/s41416-018-0136-4
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