The Challenge of Modulating Heparan Sulfate Turnover by Multitarget Heparin Derivatives.

Molecules

Department of Pathology and Immunology, School of Medicine, University of Geneva and Division of Clinical Pathology, Department of Diagnostics, Geneva University Hospitals, 1211 Geneva 14, Switzerland.

Published: January 2020

This review comes as a part of the special issue "Emerging frontiers in GAGs and mimetics". Our interest is in the manipulation of heparan sulfate (HS) turnover by employing HS mimetics/heparin derivatives that exert pleiotropic effects and are interesting for interfering at multiple levels with pathways in which HS is implicated. Due to the important role of heparanase in HS post-biosynthetic modification and catabolism, we focus on the possibility to target heparanase, at both extracellular and intracellular levels, a strategy that can be applied to many conditions, from inflammation to cancer and neurodegeneration.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7024324PMC
http://dx.doi.org/10.3390/molecules25020390DOI Listing

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