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Gelatinase B/MMP-9 in Tumour Pathogenesis and Progression

Since its original identification as a leukocyte gelatinase/type V collagenase and tumour type IV collagenase, gelatinase B/matrix metalloproteinase (MMP)-9 is now recognised as playing a central role in many aspects of tumour progression. In this review, we relate current concepts concerning the ma...

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Autores principales: Farina, Antonietta Rosella, Mackay, Andrew Reay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3980597/
https://www.ncbi.nlm.nih.gov/pubmed/24473089
http://dx.doi.org/10.3390/cancers6010240
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author Farina, Antonietta Rosella
Mackay, Andrew Reay
author_facet Farina, Antonietta Rosella
Mackay, Andrew Reay
author_sort Farina, Antonietta Rosella
collection PubMed
description Since its original identification as a leukocyte gelatinase/type V collagenase and tumour type IV collagenase, gelatinase B/matrix metalloproteinase (MMP)-9 is now recognised as playing a central role in many aspects of tumour progression. In this review, we relate current concepts concerning the many ways in which gelatinase B/MMP-9 influences tumour biology. Following a brief outline of the gelatinase B/MMP-9 gene and protein, we analyse the role(s) of gelatinase B/MMP-9 in different phases of the tumorigenic process, and compare the importance of gelatinase B/MMP-9 source in the carcinogenic process. What becomes apparent is the importance of inflammatory cell-derived gelatinase B/MMP-9 in tumour promotion, early progression and triggering of the “angiogenic switch”, the integral relationship between inflammatory, stromal and tumour components with respect to gelatinase B/MMP-9 production and activation, and the fundamental role for gelatinase B/MMP-9 in the formation and maintenance of tumour stem cell and metastatic niches. It is also apparent that gelatinase B/MMP-9 plays important tumour suppressing functions, producing endogenous angiogenesis inhibitors, promoting inflammatory anti-tumour activity, and inducing apoptosis. The fundamental roles of gelatinase B/MMP-9 in cancer biology underpins the need for specific therapeutic inhibitors of gelatinase B/MMP-9 function, the use of which must take into account and substitute for tumour-suppressing gelatinase B/MMP-9 activity and also limit inhibition of physiological gelatinase B/MMP-9 function.
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spelling pubmed-39805972014-04-09 Gelatinase B/MMP-9 in Tumour Pathogenesis and Progression Farina, Antonietta Rosella Mackay, Andrew Reay Cancers (Basel) Review Since its original identification as a leukocyte gelatinase/type V collagenase and tumour type IV collagenase, gelatinase B/matrix metalloproteinase (MMP)-9 is now recognised as playing a central role in many aspects of tumour progression. In this review, we relate current concepts concerning the many ways in which gelatinase B/MMP-9 influences tumour biology. Following a brief outline of the gelatinase B/MMP-9 gene and protein, we analyse the role(s) of gelatinase B/MMP-9 in different phases of the tumorigenic process, and compare the importance of gelatinase B/MMP-9 source in the carcinogenic process. What becomes apparent is the importance of inflammatory cell-derived gelatinase B/MMP-9 in tumour promotion, early progression and triggering of the “angiogenic switch”, the integral relationship between inflammatory, stromal and tumour components with respect to gelatinase B/MMP-9 production and activation, and the fundamental role for gelatinase B/MMP-9 in the formation and maintenance of tumour stem cell and metastatic niches. It is also apparent that gelatinase B/MMP-9 plays important tumour suppressing functions, producing endogenous angiogenesis inhibitors, promoting inflammatory anti-tumour activity, and inducing apoptosis. The fundamental roles of gelatinase B/MMP-9 in cancer biology underpins the need for specific therapeutic inhibitors of gelatinase B/MMP-9 function, the use of which must take into account and substitute for tumour-suppressing gelatinase B/MMP-9 activity and also limit inhibition of physiological gelatinase B/MMP-9 function. MDPI 2014-01-27 /pmc/articles/PMC3980597/ /pubmed/24473089 http://dx.doi.org/10.3390/cancers6010240 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Farina, Antonietta Rosella
Mackay, Andrew Reay
Gelatinase B/MMP-9 in Tumour Pathogenesis and Progression
title Gelatinase B/MMP-9 in Tumour Pathogenesis and Progression
title_full Gelatinase B/MMP-9 in Tumour Pathogenesis and Progression
title_fullStr Gelatinase B/MMP-9 in Tumour Pathogenesis and Progression
title_full_unstemmed Gelatinase B/MMP-9 in Tumour Pathogenesis and Progression
title_short Gelatinase B/MMP-9 in Tumour Pathogenesis and Progression
title_sort gelatinase b/mmp-9 in tumour pathogenesis and progression
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3980597/
https://www.ncbi.nlm.nih.gov/pubmed/24473089
http://dx.doi.org/10.3390/cancers6010240
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