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Drug repurposing for aging research using model organisms

Many increasingly prevalent diseases share a common risk factor: age. However, little is known about pharmaceutical interventions against aging, despite many genes and pathways shown to be important in the aging process and numerous studies demonstrating that genetic interventions can lead to a heal...

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Autores principales: Ziehm, Matthias, Kaur, Satwant, Ivanov, Dobril K., Ballester, Pedro J., Marcus, David, Partridge, Linda, Thornton, Janet M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595691/
https://www.ncbi.nlm.nih.gov/pubmed/28620943
http://dx.doi.org/10.1111/acel.12626
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author Ziehm, Matthias
Kaur, Satwant
Ivanov, Dobril K.
Ballester, Pedro J.
Marcus, David
Partridge, Linda
Thornton, Janet M.
author_facet Ziehm, Matthias
Kaur, Satwant
Ivanov, Dobril K.
Ballester, Pedro J.
Marcus, David
Partridge, Linda
Thornton, Janet M.
author_sort Ziehm, Matthias
collection PubMed
description Many increasingly prevalent diseases share a common risk factor: age. However, little is known about pharmaceutical interventions against aging, despite many genes and pathways shown to be important in the aging process and numerous studies demonstrating that genetic interventions can lead to a healthier aging phenotype. An important challenge is to assess the potential to repurpose existing drugs for initial testing on model organisms, where such experiments are possible. To this end, we present a new approach to rank drug‐like compounds with known mammalian targets according to their likelihood to modulate aging in the invertebrates Caenorhabditis elegans and Drosophila. Our approach combines information on genetic effects on aging, orthology relationships and sequence conservation, 3D protein structures, drug binding and bioavailability. Overall, we rank 743 different drug‐like compounds for their likelihood to modulate aging. We provide various lines of evidence for the successful enrichment of our ranking for compounds modulating aging, despite sparse public data suitable for validation. The top ranked compounds are thus prime candidates for in vivo testing of their effects on lifespan in C. elegans or Drosophila. As such, these compounds are promising as research tools and ultimately a step towards identifying drugs for a healthier human aging.
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spelling pubmed-55956912017-10-01 Drug repurposing for aging research using model organisms Ziehm, Matthias Kaur, Satwant Ivanov, Dobril K. Ballester, Pedro J. Marcus, David Partridge, Linda Thornton, Janet M. Aging Cell Original Articles Many increasingly prevalent diseases share a common risk factor: age. However, little is known about pharmaceutical interventions against aging, despite many genes and pathways shown to be important in the aging process and numerous studies demonstrating that genetic interventions can lead to a healthier aging phenotype. An important challenge is to assess the potential to repurpose existing drugs for initial testing on model organisms, where such experiments are possible. To this end, we present a new approach to rank drug‐like compounds with known mammalian targets according to their likelihood to modulate aging in the invertebrates Caenorhabditis elegans and Drosophila. Our approach combines information on genetic effects on aging, orthology relationships and sequence conservation, 3D protein structures, drug binding and bioavailability. Overall, we rank 743 different drug‐like compounds for their likelihood to modulate aging. We provide various lines of evidence for the successful enrichment of our ranking for compounds modulating aging, despite sparse public data suitable for validation. The top ranked compounds are thus prime candidates for in vivo testing of their effects on lifespan in C. elegans or Drosophila. As such, these compounds are promising as research tools and ultimately a step towards identifying drugs for a healthier human aging. John Wiley and Sons Inc. 2017-06-16 2017-10 /pmc/articles/PMC5595691/ /pubmed/28620943 http://dx.doi.org/10.1111/acel.12626 Text en © 2017 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Ziehm, Matthias
Kaur, Satwant
Ivanov, Dobril K.
Ballester, Pedro J.
Marcus, David
Partridge, Linda
Thornton, Janet M.
Drug repurposing for aging research using model organisms
title Drug repurposing for aging research using model organisms
title_full Drug repurposing for aging research using model organisms
title_fullStr Drug repurposing for aging research using model organisms
title_full_unstemmed Drug repurposing for aging research using model organisms
title_short Drug repurposing for aging research using model organisms
title_sort drug repurposing for aging research using model organisms
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595691/
https://www.ncbi.nlm.nih.gov/pubmed/28620943
http://dx.doi.org/10.1111/acel.12626
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