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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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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. |
format | Online Article Text |
id | pubmed-4241292 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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