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Discovery, development, and future application of senolytics: theories and predictions

Senescent cells accumulate with aging and at etiological sites of multiple diseases, including those accounting for most morbidity, mortality, and health costs. Senescent cells do not replicate, can release factors that cause tissue dysfunction, and yet remain viable. The discovery of senolytic drug...

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Autores principales: Wissler Gerdes, Erin O., Zhu, Yi, Tchkonia, Tamar, Kirkland, James L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7302972/
https://www.ncbi.nlm.nih.gov/pubmed/32112672
http://dx.doi.org/10.1111/febs.15264
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author Wissler Gerdes, Erin O.
Zhu, Yi
Tchkonia, Tamar
Kirkland, James L.
author_facet Wissler Gerdes, Erin O.
Zhu, Yi
Tchkonia, Tamar
Kirkland, James L.
author_sort Wissler Gerdes, Erin O.
collection PubMed
description Senescent cells accumulate with aging and at etiological sites of multiple diseases, including those accounting for most morbidity, mortality, and health costs. Senescent cells do not replicate, can release factors that cause tissue dysfunction, and yet remain viable. The discovery of senolytic drugs, agents that selectively eliminate senescent cells, created a new route for alleviating age‐related dysfunction and diseases. As anticipated for agents targeting fundamental aging mechanisms that are ‘root cause’ contributors to multiple disorders, potential applications of senolytics are protean. We review the discovery of senolytics, strategies for translation into clinical application, and promising early signals from clinical trials.
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spelling pubmed-73029722020-09-25 Discovery, development, and future application of senolytics: theories and predictions Wissler Gerdes, Erin O. Zhu, Yi Tchkonia, Tamar Kirkland, James L. FEBS J Discovery‐In‐Context Review Senescent cells accumulate with aging and at etiological sites of multiple diseases, including those accounting for most morbidity, mortality, and health costs. Senescent cells do not replicate, can release factors that cause tissue dysfunction, and yet remain viable. The discovery of senolytic drugs, agents that selectively eliminate senescent cells, created a new route for alleviating age‐related dysfunction and diseases. As anticipated for agents targeting fundamental aging mechanisms that are ‘root cause’ contributors to multiple disorders, potential applications of senolytics are protean. We review the discovery of senolytics, strategies for translation into clinical application, and promising early signals from clinical trials. John Wiley and Sons Inc. 2020-03-17 2020-06 /pmc/articles/PMC7302972/ /pubmed/32112672 http://dx.doi.org/10.1111/febs.15264 Text en © 2020 The Authors. The FEBS Journal published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Discovery‐In‐Context Review
Wissler Gerdes, Erin O.
Zhu, Yi
Tchkonia, Tamar
Kirkland, James L.
Discovery, development, and future application of senolytics: theories and predictions
title Discovery, development, and future application of senolytics: theories and predictions
title_full Discovery, development, and future application of senolytics: theories and predictions
title_fullStr Discovery, development, and future application of senolytics: theories and predictions
title_full_unstemmed Discovery, development, and future application of senolytics: theories and predictions
title_short Discovery, development, and future application of senolytics: theories and predictions
title_sort discovery, development, and future application of senolytics: theories and predictions
topic Discovery‐In‐Context Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7302972/
https://www.ncbi.nlm.nih.gov/pubmed/32112672
http://dx.doi.org/10.1111/febs.15264
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