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Current drug design to target the Semaphorin/Neuropilin/Plexin complexes

The Semaphorin/Neuropilin/Plexin (SNP) complexes control a wide range of biological processes. Consistently, activity deregulation of these complexes is associated with many diseases. The increasing knowledge on SNP had in turn validated these molecular complexes as novel therapeutic targets. Target...

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Autores principales: Meyer, Lionel A. T., Fritz, Justine, Pierdant-Mancera, Marie, Bagnard, Dominique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5160035/
https://www.ncbi.nlm.nih.gov/pubmed/27906605
http://dx.doi.org/10.1080/19336918.2016.1261785
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author Meyer, Lionel A. T.
Fritz, Justine
Pierdant-Mancera, Marie
Bagnard, Dominique
author_facet Meyer, Lionel A. T.
Fritz, Justine
Pierdant-Mancera, Marie
Bagnard, Dominique
author_sort Meyer, Lionel A. T.
collection PubMed
description The Semaphorin/Neuropilin/Plexin (SNP) complexes control a wide range of biological processes. Consistently, activity deregulation of these complexes is associated with many diseases. The increasing knowledge on SNP had in turn validated these molecular complexes as novel therapeutic targets. Targeting SNP activities by small molecules, antibodies and peptides or by soluble semaphorins have been proposed as new therapeutic approach. This review is focusing on the latest demonstration of this potential and discusses some of the key questions that need to be addressed before translating SNP targeting into clinically relevant approaches.
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spelling pubmed-51600352017-02-13 Current drug design to target the Semaphorin/Neuropilin/Plexin complexes Meyer, Lionel A. T. Fritz, Justine Pierdant-Mancera, Marie Bagnard, Dominique Cell Adh Migr Review The Semaphorin/Neuropilin/Plexin (SNP) complexes control a wide range of biological processes. Consistently, activity deregulation of these complexes is associated with many diseases. The increasing knowledge on SNP had in turn validated these molecular complexes as novel therapeutic targets. Targeting SNP activities by small molecules, antibodies and peptides or by soluble semaphorins have been proposed as new therapeutic approach. This review is focusing on the latest demonstration of this potential and discusses some of the key questions that need to be addressed before translating SNP targeting into clinically relevant approaches. Taylor & Francis 2016-12-01 /pmc/articles/PMC5160035/ /pubmed/27906605 http://dx.doi.org/10.1080/19336918.2016.1261785 Text en © 2016 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Review
Meyer, Lionel A. T.
Fritz, Justine
Pierdant-Mancera, Marie
Bagnard, Dominique
Current drug design to target the Semaphorin/Neuropilin/Plexin complexes
title Current drug design to target the Semaphorin/Neuropilin/Plexin complexes
title_full Current drug design to target the Semaphorin/Neuropilin/Plexin complexes
title_fullStr Current drug design to target the Semaphorin/Neuropilin/Plexin complexes
title_full_unstemmed Current drug design to target the Semaphorin/Neuropilin/Plexin complexes
title_short Current drug design to target the Semaphorin/Neuropilin/Plexin complexes
title_sort current drug design to target the semaphorin/neuropilin/plexin complexes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5160035/
https://www.ncbi.nlm.nih.gov/pubmed/27906605
http://dx.doi.org/10.1080/19336918.2016.1261785
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