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The Development of Assays for Heparanase Enzymatic Activity: Towards a Gold Standard

The enzyme heparanase, an endo-β-glucuronidase, degrades heparan sulfate (HS) chains on the cell surface and in the extracellular matrix. Heparanase regulates numerous biological processes that drive tumour growth, metastasis and angiogenesis. In addition to its key role in cancer progression, it ha...

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Autores principales: Chhabra, Mohit, Ferro, Vito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278452/
https://www.ncbi.nlm.nih.gov/pubmed/30441818
http://dx.doi.org/10.3390/molecules23112971
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author Chhabra, Mohit
Ferro, Vito
author_facet Chhabra, Mohit
Ferro, Vito
author_sort Chhabra, Mohit
collection PubMed
description The enzyme heparanase, an endo-β-glucuronidase, degrades heparan sulfate (HS) chains on the cell surface and in the extracellular matrix. Heparanase regulates numerous biological processes that drive tumour growth, metastasis and angiogenesis. In addition to its key role in cancer progression, it has also been implicated in an ever-growing number of other diseases, particularly those associated with inflammation. The importance of heparanase in biology has led to numerous efforts over the years to develop assays to monitor its activity and to screen for new inhibitors as potential drug candidates. Despite these efforts and the commercialization of a few kits, most heparanase assays are still complex, labour intensive, costly or have limited application. Herein we review the various methods for assaying heparanase enzymatic activity, focusing on recent developments towards new assays that hold the promise of accelerating research into this important enzyme.
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spelling pubmed-62784522018-12-13 The Development of Assays for Heparanase Enzymatic Activity: Towards a Gold Standard Chhabra, Mohit Ferro, Vito Molecules Review The enzyme heparanase, an endo-β-glucuronidase, degrades heparan sulfate (HS) chains on the cell surface and in the extracellular matrix. Heparanase regulates numerous biological processes that drive tumour growth, metastasis and angiogenesis. In addition to its key role in cancer progression, it has also been implicated in an ever-growing number of other diseases, particularly those associated with inflammation. The importance of heparanase in biology has led to numerous efforts over the years to develop assays to monitor its activity and to screen for new inhibitors as potential drug candidates. Despite these efforts and the commercialization of a few kits, most heparanase assays are still complex, labour intensive, costly or have limited application. Herein we review the various methods for assaying heparanase enzymatic activity, focusing on recent developments towards new assays that hold the promise of accelerating research into this important enzyme. MDPI 2018-11-14 /pmc/articles/PMC6278452/ /pubmed/30441818 http://dx.doi.org/10.3390/molecules23112971 Text en © 2018 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Chhabra, Mohit
Ferro, Vito
The Development of Assays for Heparanase Enzymatic Activity: Towards a Gold Standard
title The Development of Assays for Heparanase Enzymatic Activity: Towards a Gold Standard
title_full The Development of Assays for Heparanase Enzymatic Activity: Towards a Gold Standard
title_fullStr The Development of Assays for Heparanase Enzymatic Activity: Towards a Gold Standard
title_full_unstemmed The Development of Assays for Heparanase Enzymatic Activity: Towards a Gold Standard
title_short The Development of Assays for Heparanase Enzymatic Activity: Towards a Gold Standard
title_sort development of assays for heparanase enzymatic activity: towards a gold standard
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278452/
https://www.ncbi.nlm.nih.gov/pubmed/30441818
http://dx.doi.org/10.3390/molecules23112971
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