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Expressions of Matrix Metalloproteinases (MMP-2, MMP-7, and MMP-9) and Their Inhibitors (TIMP-1, TIMP-2) in Inflammatory Bowel Diseases

Crohn's disease (CD) and ulcerative colitis (UC) belong to a group of inflammatory bowel diseases (IBD). The aim of our study was to evaluate the expression of MMP-2, MMP-7, MMP-9, TIMP-1, and TIMP-2 in ulcerative colitis and Crohn's disease. The study group comprised 34 patients with UC a...

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Autores principales: Jakubowska, Katarzyna, Pryczynicz, Anna, Iwanowicz, Piotr, Niewiński, Andrzej, Maciorkowska, Elżbieta, Hapanowicz, Jerzy, Jagodzińska, Dorota, Kemona, Andrzej, Guzińska-Ustymowicz, Katarzyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4789560/
https://www.ncbi.nlm.nih.gov/pubmed/27034654
http://dx.doi.org/10.1155/2016/2456179
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author Jakubowska, Katarzyna
Pryczynicz, Anna
Iwanowicz, Piotr
Niewiński, Andrzej
Maciorkowska, Elżbieta
Hapanowicz, Jerzy
Jagodzińska, Dorota
Kemona, Andrzej
Guzińska-Ustymowicz, Katarzyna
author_facet Jakubowska, Katarzyna
Pryczynicz, Anna
Iwanowicz, Piotr
Niewiński, Andrzej
Maciorkowska, Elżbieta
Hapanowicz, Jerzy
Jagodzińska, Dorota
Kemona, Andrzej
Guzińska-Ustymowicz, Katarzyna
author_sort Jakubowska, Katarzyna
collection PubMed
description Crohn's disease (CD) and ulcerative colitis (UC) belong to a group of inflammatory bowel diseases (IBD). The aim of our study was to evaluate the expression of MMP-2, MMP-7, MMP-9, TIMP-1, and TIMP-2 in ulcerative colitis and Crohn's disease. The study group comprised 34 patients with UC and 10 patients with CD. Evaluation of MMP-2, MMP-7, MMP-9, TIMP-1, and TIMP-2 expression in tissue samples was performed using immunohistochemistry. The overexpression of MMP-9 and TIMP-1 was dominant in both the glandular epithelium and inflammatory infiltration in UC patients. In contrast, in CD subjects the positive expression of MMP-2 and TIMP-1 was in glandular tubes while mainly MMP-7 and TIMP-2 expression was in inflammatory infiltration. Metalloproteinases' expression was associated with the presence of erosions, architectural tissue changes, and inflammatory infiltration in the lamina propria of UC patients. The expression of metalloproteinase inhibitors correlated with the presence of eosinophils and neutrophils in UC and granulomas in CD patients. Our studies indicate that the overexpression of metalloproteinases and weaker expression of their inhibitors may determine the development of IBD. It appears that MMP-2, MMP-7, and MMP-9 may be a potential therapeutic target and the use of their inhibitors may significantly reduce UC progression.
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spelling pubmed-47895602016-03-31 Expressions of Matrix Metalloproteinases (MMP-2, MMP-7, and MMP-9) and Their Inhibitors (TIMP-1, TIMP-2) in Inflammatory Bowel Diseases Jakubowska, Katarzyna Pryczynicz, Anna Iwanowicz, Piotr Niewiński, Andrzej Maciorkowska, Elżbieta Hapanowicz, Jerzy Jagodzińska, Dorota Kemona, Andrzej Guzińska-Ustymowicz, Katarzyna Gastroenterol Res Pract Research Article Crohn's disease (CD) and ulcerative colitis (UC) belong to a group of inflammatory bowel diseases (IBD). The aim of our study was to evaluate the expression of MMP-2, MMP-7, MMP-9, TIMP-1, and TIMP-2 in ulcerative colitis and Crohn's disease. The study group comprised 34 patients with UC and 10 patients with CD. Evaluation of MMP-2, MMP-7, MMP-9, TIMP-1, and TIMP-2 expression in tissue samples was performed using immunohistochemistry. The overexpression of MMP-9 and TIMP-1 was dominant in both the glandular epithelium and inflammatory infiltration in UC patients. In contrast, in CD subjects the positive expression of MMP-2 and TIMP-1 was in glandular tubes while mainly MMP-7 and TIMP-2 expression was in inflammatory infiltration. Metalloproteinases' expression was associated with the presence of erosions, architectural tissue changes, and inflammatory infiltration in the lamina propria of UC patients. The expression of metalloproteinase inhibitors correlated with the presence of eosinophils and neutrophils in UC and granulomas in CD patients. Our studies indicate that the overexpression of metalloproteinases and weaker expression of their inhibitors may determine the development of IBD. It appears that MMP-2, MMP-7, and MMP-9 may be a potential therapeutic target and the use of their inhibitors may significantly reduce UC progression. Hindawi Publishing Corporation 2016 2016-02-29 /pmc/articles/PMC4789560/ /pubmed/27034654 http://dx.doi.org/10.1155/2016/2456179 Text en Copyright © 2016 Katarzyna Jakubowska et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Jakubowska, Katarzyna
Pryczynicz, Anna
Iwanowicz, Piotr
Niewiński, Andrzej
Maciorkowska, Elżbieta
Hapanowicz, Jerzy
Jagodzińska, Dorota
Kemona, Andrzej
Guzińska-Ustymowicz, Katarzyna
Expressions of Matrix Metalloproteinases (MMP-2, MMP-7, and MMP-9) and Their Inhibitors (TIMP-1, TIMP-2) in Inflammatory Bowel Diseases
title Expressions of Matrix Metalloproteinases (MMP-2, MMP-7, and MMP-9) and Their Inhibitors (TIMP-1, TIMP-2) in Inflammatory Bowel Diseases
title_full Expressions of Matrix Metalloproteinases (MMP-2, MMP-7, and MMP-9) and Their Inhibitors (TIMP-1, TIMP-2) in Inflammatory Bowel Diseases
title_fullStr Expressions of Matrix Metalloproteinases (MMP-2, MMP-7, and MMP-9) and Their Inhibitors (TIMP-1, TIMP-2) in Inflammatory Bowel Diseases
title_full_unstemmed Expressions of Matrix Metalloproteinases (MMP-2, MMP-7, and MMP-9) and Their Inhibitors (TIMP-1, TIMP-2) in Inflammatory Bowel Diseases
title_short Expressions of Matrix Metalloproteinases (MMP-2, MMP-7, and MMP-9) and Their Inhibitors (TIMP-1, TIMP-2) in Inflammatory Bowel Diseases
title_sort expressions of matrix metalloproteinases (mmp-2, mmp-7, and mmp-9) and their inhibitors (timp-1, timp-2) in inflammatory bowel diseases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4789560/
https://www.ncbi.nlm.nih.gov/pubmed/27034654
http://dx.doi.org/10.1155/2016/2456179
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