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Stressin' Sestrins take an aging fight

Sestrins (Sesns) are a family of highly conserved stress-responsive proteins, transcriptionally regulated by p53 and forkhead transcription factor that exhibit oxidoreductase activity in vitro and can protect cells from oxidative stress. However, their major biochemical and physiological function do...

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Detalles Bibliográficos
Autores principales: Budanov, Andrei V, Lee, Jun Hee, Karin, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166214/
https://www.ncbi.nlm.nih.gov/pubmed/20878915
http://dx.doi.org/10.1002/emmm.201000097
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author Budanov, Andrei V
Lee, Jun Hee
Karin, Michael
author_facet Budanov, Andrei V
Lee, Jun Hee
Karin, Michael
author_sort Budanov, Andrei V
collection PubMed
description Sestrins (Sesns) are a family of highly conserved stress-responsive proteins, transcriptionally regulated by p53 and forkhead transcription factor that exhibit oxidoreductase activity in vitro and can protect cells from oxidative stress. However, their major biochemical and physiological function does not appear to depend on their redox (reduction and oxidation) activity. Sesns promote activation of adenosine-5′-monophosphate (AMP)-dependent protein kinase in both mammals and flies. Stress-induced Sesn expression results in inhibition of the target of rapamycin complex 1 (TORC1) and the physiological and pathological implications of disrupting the Sesns-TORC1 crosstalk are now being unravelled. Detailing their mechanism of action and exploring their roles in human physiology point to exciting new insights to topics as diverse as stress, cancer, metabolism and aging.
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spelling pubmed-31662142011-10-01 Stressin' Sestrins take an aging fight Budanov, Andrei V Lee, Jun Hee Karin, Michael EMBO Mol Med Review Sestrins (Sesns) are a family of highly conserved stress-responsive proteins, transcriptionally regulated by p53 and forkhead transcription factor that exhibit oxidoreductase activity in vitro and can protect cells from oxidative stress. However, their major biochemical and physiological function does not appear to depend on their redox (reduction and oxidation) activity. Sesns promote activation of adenosine-5′-monophosphate (AMP)-dependent protein kinase in both mammals and flies. Stress-induced Sesn expression results in inhibition of the target of rapamycin complex 1 (TORC1) and the physiological and pathological implications of disrupting the Sesns-TORC1 crosstalk are now being unravelled. Detailing their mechanism of action and exploring their roles in human physiology point to exciting new insights to topics as diverse as stress, cancer, metabolism and aging. WILEY-VCH Verlag 2010-10 /pmc/articles/PMC3166214/ /pubmed/20878915 http://dx.doi.org/10.1002/emmm.201000097 Text en Copyright © 2010 EMBO Molecular Medicine
spellingShingle Review
Budanov, Andrei V
Lee, Jun Hee
Karin, Michael
Stressin' Sestrins take an aging fight
title Stressin' Sestrins take an aging fight
title_full Stressin' Sestrins take an aging fight
title_fullStr Stressin' Sestrins take an aging fight
title_full_unstemmed Stressin' Sestrins take an aging fight
title_short Stressin' Sestrins take an aging fight
title_sort stressin' sestrins take an aging fight
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166214/
https://www.ncbi.nlm.nih.gov/pubmed/20878915
http://dx.doi.org/10.1002/emmm.201000097
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