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Phenotypic Screening in C. elegans as a Tool for the Discovery of New Geroprotective Drugs

Population aging is one of the largest challenges of the 21st century. As more people live to advanced ages, the prevalence of age-related diseases and disabilities will increase placing an ever larger burden on our healthcare system. A potential solution to this conundrum is to develop treatments t...

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Autores principales: Bulterijs, Sven, Braeckman, Bart P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7463874/
https://www.ncbi.nlm.nih.gov/pubmed/32722365
http://dx.doi.org/10.3390/ph13080164
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author Bulterijs, Sven
Braeckman, Bart P.
author_facet Bulterijs, Sven
Braeckman, Bart P.
author_sort Bulterijs, Sven
collection PubMed
description Population aging is one of the largest challenges of the 21st century. As more people live to advanced ages, the prevalence of age-related diseases and disabilities will increase placing an ever larger burden on our healthcare system. A potential solution to this conundrum is to develop treatments that prevent, delay or reduce the severity of age-related diseases by decreasing the rate of the aging process. This ambition has been accomplished in model organisms through dietary, genetic and pharmacological interventions. The pharmacological approaches hold the greatest opportunity for successful translation to the clinic. The discovery of such pharmacological interventions in aging requires high-throughput screening strategies. However, the majority of screens performed for geroprotective drugs in C. elegans so far are rather low throughput. Therefore, the development of high-throughput screening strategies is of utmost importance.
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spelling pubmed-74638742020-09-04 Phenotypic Screening in C. elegans as a Tool for the Discovery of New Geroprotective Drugs Bulterijs, Sven Braeckman, Bart P. Pharmaceuticals (Basel) Review Population aging is one of the largest challenges of the 21st century. As more people live to advanced ages, the prevalence of age-related diseases and disabilities will increase placing an ever larger burden on our healthcare system. A potential solution to this conundrum is to develop treatments that prevent, delay or reduce the severity of age-related diseases by decreasing the rate of the aging process. This ambition has been accomplished in model organisms through dietary, genetic and pharmacological interventions. The pharmacological approaches hold the greatest opportunity for successful translation to the clinic. The discovery of such pharmacological interventions in aging requires high-throughput screening strategies. However, the majority of screens performed for geroprotective drugs in C. elegans so far are rather low throughput. Therefore, the development of high-throughput screening strategies is of utmost importance. MDPI 2020-07-25 /pmc/articles/PMC7463874/ /pubmed/32722365 http://dx.doi.org/10.3390/ph13080164 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Bulterijs, Sven
Braeckman, Bart P.
Phenotypic Screening in C. elegans as a Tool for the Discovery of New Geroprotective Drugs
title Phenotypic Screening in C. elegans as a Tool for the Discovery of New Geroprotective Drugs
title_full Phenotypic Screening in C. elegans as a Tool for the Discovery of New Geroprotective Drugs
title_fullStr Phenotypic Screening in C. elegans as a Tool for the Discovery of New Geroprotective Drugs
title_full_unstemmed Phenotypic Screening in C. elegans as a Tool for the Discovery of New Geroprotective Drugs
title_short Phenotypic Screening in C. elegans as a Tool for the Discovery of New Geroprotective Drugs
title_sort phenotypic screening in c. elegans as a tool for the discovery of new geroprotective drugs
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7463874/
https://www.ncbi.nlm.nih.gov/pubmed/32722365
http://dx.doi.org/10.3390/ph13080164
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