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Targeting the SUMO pathway for neuroprotection in brain ischaemia

Small ubiquitin-like modifier (SUMO) conjugation (SUMOylation) is a post-translational protein modification that modulates almost all major cellular processes, and has been implicated in many human diseases. A growing body of evidence from in vitro and in vivo studies demonstrates that increasing gl...

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Autores principales: Yang, Wei, Sheng, Huaxin, Wang, Haichen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435206/
https://www.ncbi.nlm.nih.gov/pubmed/28959470
http://dx.doi.org/10.1136/svn-2016-000031
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author Yang, Wei
Sheng, Huaxin
Wang, Haichen
author_facet Yang, Wei
Sheng, Huaxin
Wang, Haichen
author_sort Yang, Wei
collection PubMed
description Small ubiquitin-like modifier (SUMO) conjugation (SUMOylation) is a post-translational protein modification that modulates almost all major cellular processes, and has been implicated in many human diseases. A growing body of evidence from in vitro and in vivo studies demonstrates that increasing global levels of SUMO conjugated proteins (global SUMOylation) protects cells against ischaemia-induced damage, while suppressing global SUMOylation promotes cell injury after ischaemia. Indeed, SUMOylation has emerged as a potential therapeutic target for neuroprotection in brain ischaemia, including global brain ischaemia and focal brain ischaemia (ischaemic stroke). Here, we summarise findings on the role of SUMOylation in human diseases, brain ischaemia in particular, and review recent developments in drug discovery targeting SUMOylation with a major focus on its neuroprotective applications.
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spelling pubmed-54352062017-09-28 Targeting the SUMO pathway for neuroprotection in brain ischaemia Yang, Wei Sheng, Huaxin Wang, Haichen Stroke Vasc Neurol Review Small ubiquitin-like modifier (SUMO) conjugation (SUMOylation) is a post-translational protein modification that modulates almost all major cellular processes, and has been implicated in many human diseases. A growing body of evidence from in vitro and in vivo studies demonstrates that increasing global levels of SUMO conjugated proteins (global SUMOylation) protects cells against ischaemia-induced damage, while suppressing global SUMOylation promotes cell injury after ischaemia. Indeed, SUMOylation has emerged as a potential therapeutic target for neuroprotection in brain ischaemia, including global brain ischaemia and focal brain ischaemia (ischaemic stroke). Here, we summarise findings on the role of SUMOylation in human diseases, brain ischaemia in particular, and review recent developments in drug discovery targeting SUMOylation with a major focus on its neuroprotective applications. BMJ Publishing Group 2016-10-25 /pmc/articles/PMC5435206/ /pubmed/28959470 http://dx.doi.org/10.1136/svn-2016-000031 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Review
Yang, Wei
Sheng, Huaxin
Wang, Haichen
Targeting the SUMO pathway for neuroprotection in brain ischaemia
title Targeting the SUMO pathway for neuroprotection in brain ischaemia
title_full Targeting the SUMO pathway for neuroprotection in brain ischaemia
title_fullStr Targeting the SUMO pathway for neuroprotection in brain ischaemia
title_full_unstemmed Targeting the SUMO pathway for neuroprotection in brain ischaemia
title_short Targeting the SUMO pathway for neuroprotection in brain ischaemia
title_sort targeting the sumo pathway for neuroprotection in brain ischaemia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435206/
https://www.ncbi.nlm.nih.gov/pubmed/28959470
http://dx.doi.org/10.1136/svn-2016-000031
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