Cargando…

Identification of neutrophil-derived proteases and angiotensin II as biomarkers of cancer cachexia

BACKGROUND: Cachexia is a metabolic disorder characterised by muscle wasting, diminished response to anti-cancer treatments and poor quality of life. Our objective was to identify blood-based biomarkers of cachexia in advanced cancer patients. Hence, we characterised the plasma cytokine and blood ce...

Descripción completa

Detalles Bibliográficos
Autores principales: Penafuerte, Claudia A, Gagnon, Bruno, Sirois, Jacinthe, Murphy, Jessica, MacDonald, Neil, Tremblay, Michel L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4800302/
https://www.ncbi.nlm.nih.gov/pubmed/26954714
http://dx.doi.org/10.1038/bjc.2016.3
_version_ 1782422459584086016
author Penafuerte, Claudia A
Gagnon, Bruno
Sirois, Jacinthe
Murphy, Jessica
MacDonald, Neil
Tremblay, Michel L
author_facet Penafuerte, Claudia A
Gagnon, Bruno
Sirois, Jacinthe
Murphy, Jessica
MacDonald, Neil
Tremblay, Michel L
author_sort Penafuerte, Claudia A
collection PubMed
description BACKGROUND: Cachexia is a metabolic disorder characterised by muscle wasting, diminished response to anti-cancer treatments and poor quality of life. Our objective was to identify blood-based biomarkers of cachexia in advanced cancer patients. Hence, we characterised the plasma cytokine and blood cell mRNA profiles of patients grouped in three cohorts: patients with cachexia, pre-cachexia (no cachexia but high CRP levels: ⩾5 mg l(−1)) and no cachexia (no cachexia and CRP: <5 mg l(−1)). METHODS: A total of 122 newly diagnosed cancer patients with seven cancer types were studied prior to their initial therapy. Plasma levels of 22 cytokines were quantified using the bio-plex technology. mRNAs isolated from whole blood and expression profiles were determined by the chip array technology and Ingenuity Pathway Analysis (IPA) software. RESULTS: In comparison with non-cachectic individuals, both pre-cachectic and cachectic patients showed an increase (⩾1.5-folds) in mRNA expression of neutrophil-derived proteases (NDPs) and significantly elevated angiotensin II (Ang II) (P=0.005 and P=0.02, respectively), TGFβ1 (P=0.042 and P<0.0001, respectively) and CRP (both P<0.0001) in the plasma. Moreover, cachectic patients displayed a significant increase in IL-6 (P=0.005), IL-8 (P=0.001) and absolute neutrophil counts (P=0.007). CONCLUSIONS: Ang II, TGFβ1, CRP and NDP are blood biomarkers for cancer cachexia. These findings contribute to early diagnosis and prevention of cachexia.
format Online
Article
Text
id pubmed-4800302
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-48003022017-03-15 Identification of neutrophil-derived proteases and angiotensin II as biomarkers of cancer cachexia Penafuerte, Claudia A Gagnon, Bruno Sirois, Jacinthe Murphy, Jessica MacDonald, Neil Tremblay, Michel L Br J Cancer Molecular Diagnostics BACKGROUND: Cachexia is a metabolic disorder characterised by muscle wasting, diminished response to anti-cancer treatments and poor quality of life. Our objective was to identify blood-based biomarkers of cachexia in advanced cancer patients. Hence, we characterised the plasma cytokine and blood cell mRNA profiles of patients grouped in three cohorts: patients with cachexia, pre-cachexia (no cachexia but high CRP levels: ⩾5 mg l(−1)) and no cachexia (no cachexia and CRP: <5 mg l(−1)). METHODS: A total of 122 newly diagnosed cancer patients with seven cancer types were studied prior to their initial therapy. Plasma levels of 22 cytokines were quantified using the bio-plex technology. mRNAs isolated from whole blood and expression profiles were determined by the chip array technology and Ingenuity Pathway Analysis (IPA) software. RESULTS: In comparison with non-cachectic individuals, both pre-cachectic and cachectic patients showed an increase (⩾1.5-folds) in mRNA expression of neutrophil-derived proteases (NDPs) and significantly elevated angiotensin II (Ang II) (P=0.005 and P=0.02, respectively), TGFβ1 (P=0.042 and P<0.0001, respectively) and CRP (both P<0.0001) in the plasma. Moreover, cachectic patients displayed a significant increase in IL-6 (P=0.005), IL-8 (P=0.001) and absolute neutrophil counts (P=0.007). CONCLUSIONS: Ang II, TGFβ1, CRP and NDP are blood biomarkers for cancer cachexia. These findings contribute to early diagnosis and prevention of cachexia. Nature Publishing Group 2016-03-15 2016-03-08 /pmc/articles/PMC4800302/ /pubmed/26954714 http://dx.doi.org/10.1038/bjc.2016.3 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Molecular Diagnostics
Penafuerte, Claudia A
Gagnon, Bruno
Sirois, Jacinthe
Murphy, Jessica
MacDonald, Neil
Tremblay, Michel L
Identification of neutrophil-derived proteases and angiotensin II as biomarkers of cancer cachexia
title Identification of neutrophil-derived proteases and angiotensin II as biomarkers of cancer cachexia
title_full Identification of neutrophil-derived proteases and angiotensin II as biomarkers of cancer cachexia
title_fullStr Identification of neutrophil-derived proteases and angiotensin II as biomarkers of cancer cachexia
title_full_unstemmed Identification of neutrophil-derived proteases and angiotensin II as biomarkers of cancer cachexia
title_short Identification of neutrophil-derived proteases and angiotensin II as biomarkers of cancer cachexia
title_sort identification of neutrophil-derived proteases and angiotensin ii as biomarkers of cancer cachexia
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4800302/
https://www.ncbi.nlm.nih.gov/pubmed/26954714
http://dx.doi.org/10.1038/bjc.2016.3
work_keys_str_mv AT penafuerteclaudiaa identificationofneutrophilderivedproteasesandangiotensiniiasbiomarkersofcancercachexia
AT gagnonbruno identificationofneutrophilderivedproteasesandangiotensiniiasbiomarkersofcancercachexia
AT siroisjacinthe identificationofneutrophilderivedproteasesandangiotensiniiasbiomarkersofcancercachexia
AT murphyjessica identificationofneutrophilderivedproteasesandangiotensiniiasbiomarkersofcancercachexia
AT macdonaldneil identificationofneutrophilderivedproteasesandangiotensiniiasbiomarkersofcancercachexia
AT tremblaymichell identificationofneutrophilderivedproteasesandangiotensiniiasbiomarkersofcancercachexia