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Protease inhibition as new therapeutic strategy for GI diseases
The GI tract is the most exposed organ to proteases, both in physiological and pathophysiological conditions. For digestive purposes, the lumen of the upper GI tract contains large amounts of pancreatic proteases, but studies have also demonstrated increased proteolytic activity into mucosal tissues...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BMJ Publishing Group
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941139/ https://www.ncbi.nlm.nih.gov/pubmed/27196587 http://dx.doi.org/10.1136/gutjnl-2015-309147 |
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author | Vergnolle, Nathalie |
author_facet | Vergnolle, Nathalie |
author_sort | Vergnolle, Nathalie |
collection | PubMed |
description | The GI tract is the most exposed organ to proteases, both in physiological and pathophysiological conditions. For digestive purposes, the lumen of the upper GI tract contains large amounts of pancreatic proteases, but studies have also demonstrated increased proteolytic activity into mucosal tissues (both in the upper and lower GI tract), associated with pathological conditions. This review aims at outlining the evidences for dysregulated proteolytic homeostasis in GI diseases and the pathogenic mechanisms of increased proteolytic activity. The therapeutic potential of protease inhibition in GI diseases is discussed, with a particular focus on IBDs, functional GI disorders and colorectal cancer. |
format | Online Article Text |
id | pubmed-4941139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49411392016-07-13 Protease inhibition as new therapeutic strategy for GI diseases Vergnolle, Nathalie Gut Recent Advances in Basic Science The GI tract is the most exposed organ to proteases, both in physiological and pathophysiological conditions. For digestive purposes, the lumen of the upper GI tract contains large amounts of pancreatic proteases, but studies have also demonstrated increased proteolytic activity into mucosal tissues (both in the upper and lower GI tract), associated with pathological conditions. This review aims at outlining the evidences for dysregulated proteolytic homeostasis in GI diseases and the pathogenic mechanisms of increased proteolytic activity. The therapeutic potential of protease inhibition in GI diseases is discussed, with a particular focus on IBDs, functional GI disorders and colorectal cancer. BMJ Publishing Group 2016-07 2016-04-12 /pmc/articles/PMC4941139/ /pubmed/27196587 http://dx.doi.org/10.1136/gutjnl-2015-309147 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Recent Advances in Basic Science Vergnolle, Nathalie Protease inhibition as new therapeutic strategy for GI diseases |
title | Protease inhibition as new therapeutic strategy for GI diseases |
title_full | Protease inhibition as new therapeutic strategy for GI diseases |
title_fullStr | Protease inhibition as new therapeutic strategy for GI diseases |
title_full_unstemmed | Protease inhibition as new therapeutic strategy for GI diseases |
title_short | Protease inhibition as new therapeutic strategy for GI diseases |
title_sort | protease inhibition as new therapeutic strategy for gi diseases |
topic | Recent Advances in Basic Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4941139/ https://www.ncbi.nlm.nih.gov/pubmed/27196587 http://dx.doi.org/10.1136/gutjnl-2015-309147 |
work_keys_str_mv | AT vergnollenathalie proteaseinhibitionasnewtherapeuticstrategyforgidiseases |