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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science Pub. Co
2016
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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. |
format | Online Article Text |
id | pubmed-5119498 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier Science Pub. Co |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT lipinachristopher isredd1ametaboliceminencegrise AT hundalharinders isredd1ametaboliceminencegrise |