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Potential repurposing of oncology drugs for the treatment of Alzheimer's disease

Alzheimer's disease (AD) is the most common form of neurodegenerative dementia, affecting about 30 million people worldwide. Despite recent advances in understanding its molecular pathology, no mechanism-based drugs are currently available that can halt the progression of AD. Because amyloid-β-...

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Detalles Bibliográficos
Autor principal: Araki, Wataru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655040/
https://www.ncbi.nlm.nih.gov/pubmed/23531187
http://dx.doi.org/10.1186/1741-7015-11-82
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author Araki, Wataru
author_facet Araki, Wataru
author_sort Araki, Wataru
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description Alzheimer's disease (AD) is the most common form of neurodegenerative dementia, affecting about 30 million people worldwide. Despite recent advances in understanding its molecular pathology, no mechanism-based drugs are currently available that can halt the progression of AD. Because amyloid-β-peptide (Aβ), a primary component of senile plaques, is thought to be a central pathogenic culprit, several disease-modifying therapies are being developed, including inhibitors of Aβ-producing proteases and immunotherapies with anti-Aβ antibodies. Drug repositioning or repurposing is regarded as a complementary and reasonable approach to identify new drug candidates for AD. This commentary will discuss the clinical relevance of an attractive candidate compound reported in a recent paper by Hayes et al. (BMC Medicine 2013) as well as perspectives regarding the possible repositioning of oncology drugs for the treatment of AD. See related research article here http://www.biomedcentral.com/1741-7015/11/81
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spelling pubmed-36550402013-05-20 Potential repurposing of oncology drugs for the treatment of Alzheimer's disease Araki, Wataru BMC Med Commentary Alzheimer's disease (AD) is the most common form of neurodegenerative dementia, affecting about 30 million people worldwide. Despite recent advances in understanding its molecular pathology, no mechanism-based drugs are currently available that can halt the progression of AD. Because amyloid-β-peptide (Aβ), a primary component of senile plaques, is thought to be a central pathogenic culprit, several disease-modifying therapies are being developed, including inhibitors of Aβ-producing proteases and immunotherapies with anti-Aβ antibodies. Drug repositioning or repurposing is regarded as a complementary and reasonable approach to identify new drug candidates for AD. This commentary will discuss the clinical relevance of an attractive candidate compound reported in a recent paper by Hayes et al. (BMC Medicine 2013) as well as perspectives regarding the possible repositioning of oncology drugs for the treatment of AD. See related research article here http://www.biomedcentral.com/1741-7015/11/81 BioMed Central 2013-03-26 /pmc/articles/PMC3655040/ /pubmed/23531187 http://dx.doi.org/10.1186/1741-7015-11-82 Text en Copyright © 2013 Araki; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Araki, Wataru
Potential repurposing of oncology drugs for the treatment of Alzheimer's disease
title Potential repurposing of oncology drugs for the treatment of Alzheimer's disease
title_full Potential repurposing of oncology drugs for the treatment of Alzheimer's disease
title_fullStr Potential repurposing of oncology drugs for the treatment of Alzheimer's disease
title_full_unstemmed Potential repurposing of oncology drugs for the treatment of Alzheimer's disease
title_short Potential repurposing of oncology drugs for the treatment of Alzheimer's disease
title_sort potential repurposing of oncology drugs for the treatment of alzheimer's disease
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655040/
https://www.ncbi.nlm.nih.gov/pubmed/23531187
http://dx.doi.org/10.1186/1741-7015-11-82
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