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Is REDD1 a Metabolic Éminence Grise?

Regulated in development and DNA damage response 1 (REDD1) has been functionally linked to the control of diverse cellular processes due, at least in part, to its ability to repress mammalian or mechanistic Target of Rapamycin (mTOR) Complex-1 (mTORC1), a key protein complex controlled by hormonal a...

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Detalles Bibliográficos
Autores principales: Lipina, Christopher, Hundal, Harinder S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Pub. Co 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5119498/
https://www.ncbi.nlm.nih.gov/pubmed/27613400
http://dx.doi.org/10.1016/j.tem.2016.08.005
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author Lipina, Christopher
Hundal, Harinder S
author_facet Lipina, Christopher
Hundal, Harinder S
author_sort Lipina, Christopher
collection PubMed
description Regulated in development and DNA damage response 1 (REDD1) has been functionally linked to the control of diverse cellular processes due, at least in part, to its ability to repress mammalian or mechanistic Target of Rapamycin (mTOR) Complex-1 (mTORC1), a key protein complex controlled by hormonal and nutrient cues. Notably, emerging evidence suggests that REDD1 also regulates several pathways involved in modulating energy balance and metabolism. Herein, we discuss evidence implicating REDD1 as a key modulator of insulin action and metabolic function, including its potential contribution to mitochondrial biology and pancreatic islet function. Collectively, the available evidence suggests that REDD1 has a more prominent role in energy homeostasis than was previously thought, and implicates REDD1 as a potential therapeutic target for treatment of metabolic disorders.
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spelling pubmed-51194982016-12-01 Is REDD1 a Metabolic Éminence Grise? Lipina, Christopher Hundal, Harinder S Trends Endocrinol Metab Review Regulated in development and DNA damage response 1 (REDD1) has been functionally linked to the control of diverse cellular processes due, at least in part, to its ability to repress mammalian or mechanistic Target of Rapamycin (mTOR) Complex-1 (mTORC1), a key protein complex controlled by hormonal and nutrient cues. Notably, emerging evidence suggests that REDD1 also regulates several pathways involved in modulating energy balance and metabolism. Herein, we discuss evidence implicating REDD1 as a key modulator of insulin action and metabolic function, including its potential contribution to mitochondrial biology and pancreatic islet function. Collectively, the available evidence suggests that REDD1 has a more prominent role in energy homeostasis than was previously thought, and implicates REDD1 as a potential therapeutic target for treatment of metabolic disorders. Elsevier Science Pub. Co 2016-12 /pmc/articles/PMC5119498/ /pubmed/27613400 http://dx.doi.org/10.1016/j.tem.2016.08.005 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Lipina, Christopher
Hundal, Harinder S
Is REDD1 a Metabolic Éminence Grise?
title Is REDD1 a Metabolic Éminence Grise?
title_full Is REDD1 a Metabolic Éminence Grise?
title_fullStr Is REDD1 a Metabolic Éminence Grise?
title_full_unstemmed Is REDD1 a Metabolic Éminence Grise?
title_short Is REDD1 a Metabolic Éminence Grise?
title_sort is redd1 a metabolic éminence grise?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5119498/
https://www.ncbi.nlm.nih.gov/pubmed/27613400
http://dx.doi.org/10.1016/j.tem.2016.08.005
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