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Heat Shock Protein 70 in Alzheimer's Disease

Alzheimer's disease (AD) is the most common neurodegenerative disease that caused dementia which has no effective treatment. Growing evidence has demonstrated that AD is a “protein misfolding disorder” that exhibits common features of misfolded, aggregation-prone proteins and selective cell los...

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Autores principales: Lu, Rui-Chun, Tan, Meng-Shan, Wang, Hao, Xie, An-Mu, Yu, Jin-Tai, Tan, Lan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241292/
https://www.ncbi.nlm.nih.gov/pubmed/25431764
http://dx.doi.org/10.1155/2014/435203
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author Lu, Rui-Chun
Tan, Meng-Shan
Wang, Hao
Xie, An-Mu
Yu, Jin-Tai
Tan, Lan
author_facet Lu, Rui-Chun
Tan, Meng-Shan
Wang, Hao
Xie, An-Mu
Yu, Jin-Tai
Tan, Lan
author_sort Lu, Rui-Chun
collection PubMed
description Alzheimer's disease (AD) is the most common neurodegenerative disease that caused dementia which has no effective treatment. Growing evidence has demonstrated that AD is a “protein misfolding disorder” that exhibits common features of misfolded, aggregation-prone proteins and selective cell loss in the mature nervous system. Heat shock protein 70 (HSP70) attracts extensive attention worldwide, because it plays a crucial role in preventing protein misfolding and inhibiting aggregation and represents a class of proteins potentially involved in AD pathogenesis. Numerous studies have indicated that HSP70 could suppress the progression of AD with in vitro and in vivo experiments. Thus, targeting HSP70 and the related compounds might represent a promising strategy for the treatment of AD.
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spelling pubmed-42412922014-11-27 Heat Shock Protein 70 in Alzheimer's Disease Lu, Rui-Chun Tan, Meng-Shan Wang, Hao Xie, An-Mu Yu, Jin-Tai Tan, Lan Biomed Res Int Review Article Alzheimer's disease (AD) is the most common neurodegenerative disease that caused dementia which has no effective treatment. Growing evidence has demonstrated that AD is a “protein misfolding disorder” that exhibits common features of misfolded, aggregation-prone proteins and selective cell loss in the mature nervous system. Heat shock protein 70 (HSP70) attracts extensive attention worldwide, because it plays a crucial role in preventing protein misfolding and inhibiting aggregation and represents a class of proteins potentially involved in AD pathogenesis. Numerous studies have indicated that HSP70 could suppress the progression of AD with in vitro and in vivo experiments. Thus, targeting HSP70 and the related compounds might represent a promising strategy for the treatment of AD. Hindawi Publishing Corporation 2014 2014-11-06 /pmc/articles/PMC4241292/ /pubmed/25431764 http://dx.doi.org/10.1155/2014/435203 Text en Copyright © 2014 Rui-Chun Lu et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Lu, Rui-Chun
Tan, Meng-Shan
Wang, Hao
Xie, An-Mu
Yu, Jin-Tai
Tan, Lan
Heat Shock Protein 70 in Alzheimer's Disease
title Heat Shock Protein 70 in Alzheimer's Disease
title_full Heat Shock Protein 70 in Alzheimer's Disease
title_fullStr Heat Shock Protein 70 in Alzheimer's Disease
title_full_unstemmed Heat Shock Protein 70 in Alzheimer's Disease
title_short Heat Shock Protein 70 in Alzheimer's Disease
title_sort heat shock protein 70 in alzheimer's disease
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241292/
https://www.ncbi.nlm.nih.gov/pubmed/25431764
http://dx.doi.org/10.1155/2014/435203
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