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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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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. |
format | Online Article Text |
id | pubmed-5160035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
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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