Targeting Galectins With Glycomimetics

Among glycan-binding proteins, galectins, β-galactoside-binding lectins, exhibit relevant biological roles and are implicated in many diseases, such as cancer and inflammation. Their involvement in crucial pathologies makes them interesting targets for drug discovery. In this review, we gather the l...

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Main Authors: Sara Bertuzzi, Jon I. Quintana, Ana Ardá, Ana Gimeno, Jesús Jiménez-Barbero
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-08-01
Series:Frontiers in Chemistry
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fchem.2020.00593/full
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spelling doaj-b9888bc8ebe64bb4a5cd88a473b703262020-11-25T03:26:29ZengFrontiers Media S.A.Frontiers in Chemistry2296-26462020-08-01810.3389/fchem.2020.00593552915Targeting Galectins With GlycomimeticsSara Bertuzzi0Jon I. Quintana1Ana Ardá2Ana Gimeno3Jesús Jiménez-Barbero4Jesús Jiménez-Barbero5Jesús Jiménez-Barbero6CIC bioGUNE, Basque Research Technology Alliance, Derio, SpainCIC bioGUNE, Basque Research Technology Alliance, Derio, SpainCIC bioGUNE, Basque Research Technology Alliance, Derio, SpainCIC bioGUNE, Basque Research Technology Alliance, Derio, SpainCIC bioGUNE, Basque Research Technology Alliance, Derio, SpainIkerbasque, Basque Foundation for Science, Bilbao, SpainDepartment of Organic Chemistry II, Faculty of Science and Technology, University of the Basque Country - UPV-EHU, Leioa, SpainAmong glycan-binding proteins, galectins, β-galactoside-binding lectins, exhibit relevant biological roles and are implicated in many diseases, such as cancer and inflammation. Their involvement in crucial pathologies makes them interesting targets for drug discovery. In this review, we gather the last approaches toward the specific design of glycomimetics as potential drugs against galectins. Different approaches, either using specific glycomimetic molecules decorated with key functional groups or employing multivalent presentations of lactose and N-acetyl lactosamine analogs, have provided promising results for binding and modulating different galectins. The review highlights the results obtained with these approximations, from the employment of S-glycosyl compounds to peptidomimetics and multivalent glycopolymers, mostly employed to recognize and/or detect hGal-1 and hGal-3.https://www.frontiersin.org/article/10.3389/fchem.2020.00593/fullgalectinsglycomimeticsglycansmolecular recogntiondrug design
collection DOAJ
language English
format Article
sources DOAJ
author Sara Bertuzzi
Jon I. Quintana
Ana Ardá
Ana Gimeno
Jesús Jiménez-Barbero
Jesús Jiménez-Barbero
Jesús Jiménez-Barbero
spellingShingle Sara Bertuzzi
Jon I. Quintana
Ana Ardá
Ana Gimeno
Jesús Jiménez-Barbero
Jesús Jiménez-Barbero
Jesús Jiménez-Barbero
Targeting Galectins With Glycomimetics
Frontiers in Chemistry
galectins
glycomimetics
glycans
molecular recogntion
drug design
author_facet Sara Bertuzzi
Jon I. Quintana
Ana Ardá
Ana Gimeno
Jesús Jiménez-Barbero
Jesús Jiménez-Barbero
Jesús Jiménez-Barbero
author_sort Sara Bertuzzi
title Targeting Galectins With Glycomimetics
title_short Targeting Galectins With Glycomimetics
title_full Targeting Galectins With Glycomimetics
title_fullStr Targeting Galectins With Glycomimetics
title_full_unstemmed Targeting Galectins With Glycomimetics
title_sort targeting galectins with glycomimetics
publisher Frontiers Media S.A.
series Frontiers in Chemistry
issn 2296-2646
publishDate 2020-08-01
description Among glycan-binding proteins, galectins, β-galactoside-binding lectins, exhibit relevant biological roles and are implicated in many diseases, such as cancer and inflammation. Their involvement in crucial pathologies makes them interesting targets for drug discovery. In this review, we gather the last approaches toward the specific design of glycomimetics as potential drugs against galectins. Different approaches, either using specific glycomimetic molecules decorated with key functional groups or employing multivalent presentations of lactose and N-acetyl lactosamine analogs, have provided promising results for binding and modulating different galectins. The review highlights the results obtained with these approximations, from the employment of S-glycosyl compounds to peptidomimetics and multivalent glycopolymers, mostly employed to recognize and/or detect hGal-1 and hGal-3.
topic galectins
glycomimetics
glycans
molecular recogntion
drug design
url https://www.frontiersin.org/article/10.3389/fchem.2020.00593/full
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