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A pilot study on faecal MMP-9: a new noninvasive diagnostic marker of colorectal cancer

BACKGROUND: Colorectal cancer (CRC) is one of the leading malignancies worldwide, therefore cheap noninvasive screening methods are of great importance. Matrix-metalloproteinase-9 (MMP-9) has a role in the progression of CRC, and its level is elevated in tumour biopsies. Faecal MMP-9 levels are incr...

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Autores principales: Annaházi, Anita, Ábrahám, Szabolcs, Farkas, Klaudia, Rosztóczy, András, Inczefi, Orsolya, Földesi, Imre, Szűcs, Mónika, Rutka, Mariann, Theodorou, Vassilia, Eutamene, Helene, Bueno, Lionel, Lázár, György, Wittmann, Tibor, Molnár, Tamás, Róka, Richárd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4984857/
https://www.ncbi.nlm.nih.gov/pubmed/26908323
http://dx.doi.org/10.1038/bjc.2016.31
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author Annaházi, Anita
Ábrahám, Szabolcs
Farkas, Klaudia
Rosztóczy, András
Inczefi, Orsolya
Földesi, Imre
Szűcs, Mónika
Rutka, Mariann
Theodorou, Vassilia
Eutamene, Helene
Bueno, Lionel
Lázár, György
Wittmann, Tibor
Molnár, Tamás
Róka, Richárd
author_facet Annaházi, Anita
Ábrahám, Szabolcs
Farkas, Klaudia
Rosztóczy, András
Inczefi, Orsolya
Földesi, Imre
Szűcs, Mónika
Rutka, Mariann
Theodorou, Vassilia
Eutamene, Helene
Bueno, Lionel
Lázár, György
Wittmann, Tibor
Molnár, Tamás
Róka, Richárd
author_sort Annaházi, Anita
collection PubMed
description BACKGROUND: Colorectal cancer (CRC) is one of the leading malignancies worldwide, therefore cheap noninvasive screening methods are of great importance. Matrix-metalloproteinase-9 (MMP-9) has a role in the progression of CRC, and its level is elevated in tumour biopsies. Faecal MMP-9 levels are increased in active ulcerative colitis patients, but in CRC patients, they have never been measured. We aimed to assess the faecal MMP-9 levels in patients undergoing total colonoscopy according to endoscopic and histological diagnosis. METHODS: One hundred and nine patients provided faecal samples for MMP-9 analysis. A total colonoscopy was performed; suspicious lesions were evaluated by histology. Faecal MMP-9 levels were measured by ELISA. RESULTS: The number of patients allocated to different groups were: negative/diverticulosis: 34 (referred to as controls); hyperplastic polyps: 15; adenomas: 32 (22 at high risk); and CRC: 28. Faecal MMP-9 was significantly increased in CRC compared with all other groups (P<0.001). Faecal MMP-9 was suitable to distinguish CRC patients from controls (sensitivity: 89.3% specificity: 91.2%). By means of a lower cutoff level, faecal MMP-9 identified high-risk adenomas besides CRC (sensitivity: 76% specificity: 85.3%). This lower cutoff level screened 59% of high-risk adenomas. CONCLUSIONS: Faecal MMP-9 may be a promising new noninvasive marker in CRC.
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spelling pubmed-49848572017-03-29 A pilot study on faecal MMP-9: a new noninvasive diagnostic marker of colorectal cancer Annaházi, Anita Ábrahám, Szabolcs Farkas, Klaudia Rosztóczy, András Inczefi, Orsolya Földesi, Imre Szűcs, Mónika Rutka, Mariann Theodorou, Vassilia Eutamene, Helene Bueno, Lionel Lázár, György Wittmann, Tibor Molnár, Tamás Róka, Richárd Br J Cancer Translational Therapeutics BACKGROUND: Colorectal cancer (CRC) is one of the leading malignancies worldwide, therefore cheap noninvasive screening methods are of great importance. Matrix-metalloproteinase-9 (MMP-9) has a role in the progression of CRC, and its level is elevated in tumour biopsies. Faecal MMP-9 levels are increased in active ulcerative colitis patients, but in CRC patients, they have never been measured. We aimed to assess the faecal MMP-9 levels in patients undergoing total colonoscopy according to endoscopic and histological diagnosis. METHODS: One hundred and nine patients provided faecal samples for MMP-9 analysis. A total colonoscopy was performed; suspicious lesions were evaluated by histology. Faecal MMP-9 levels were measured by ELISA. RESULTS: The number of patients allocated to different groups were: negative/diverticulosis: 34 (referred to as controls); hyperplastic polyps: 15; adenomas: 32 (22 at high risk); and CRC: 28. Faecal MMP-9 was significantly increased in CRC compared with all other groups (P<0.001). Faecal MMP-9 was suitable to distinguish CRC patients from controls (sensitivity: 89.3% specificity: 91.2%). By means of a lower cutoff level, faecal MMP-9 identified high-risk adenomas besides CRC (sensitivity: 76% specificity: 85.3%). This lower cutoff level screened 59% of high-risk adenomas. CONCLUSIONS: Faecal MMP-9 may be a promising new noninvasive marker in CRC. Nature Publishing Group 2016-03-29 2016-02-23 /pmc/articles/PMC4984857/ /pubmed/26908323 http://dx.doi.org/10.1038/bjc.2016.31 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 Translational Therapeutics
Annaházi, Anita
Ábrahám, Szabolcs
Farkas, Klaudia
Rosztóczy, András
Inczefi, Orsolya
Földesi, Imre
Szűcs, Mónika
Rutka, Mariann
Theodorou, Vassilia
Eutamene, Helene
Bueno, Lionel
Lázár, György
Wittmann, Tibor
Molnár, Tamás
Róka, Richárd
A pilot study on faecal MMP-9: a new noninvasive diagnostic marker of colorectal cancer
title A pilot study on faecal MMP-9: a new noninvasive diagnostic marker of colorectal cancer
title_full A pilot study on faecal MMP-9: a new noninvasive diagnostic marker of colorectal cancer
title_fullStr A pilot study on faecal MMP-9: a new noninvasive diagnostic marker of colorectal cancer
title_full_unstemmed A pilot study on faecal MMP-9: a new noninvasive diagnostic marker of colorectal cancer
title_short A pilot study on faecal MMP-9: a new noninvasive diagnostic marker of colorectal cancer
title_sort pilot study on faecal mmp-9: a new noninvasive diagnostic marker of colorectal cancer
topic Translational Therapeutics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4984857/
https://www.ncbi.nlm.nih.gov/pubmed/26908323
http://dx.doi.org/10.1038/bjc.2016.31
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