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Role of FoxO1 in regulating autophagy in type 2 diabetes mellitus (Review)

Type 2 diabetes mellitus (T2DM) is a major chronic disease that is characterized by pancreatic β-cell dysfunction and insulin resistance. Autophagy is a highly conserved intracellular recycling pathway and is involved in regulating intracellular homeostasis. Transcription factor Forkhead box O1 (Fox...

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Autores principales: Li, Xiudan, Wan, Tingting, Li, Yanbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120662/
https://www.ncbi.nlm.nih.gov/pubmed/34007316
http://dx.doi.org/10.3892/etm.2021.10139
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author Li, Xiudan
Wan, Tingting
Li, Yanbo
author_facet Li, Xiudan
Wan, Tingting
Li, Yanbo
author_sort Li, Xiudan
collection PubMed
description Type 2 diabetes mellitus (T2DM) is a major chronic disease that is characterized by pancreatic β-cell dysfunction and insulin resistance. Autophagy is a highly conserved intracellular recycling pathway and is involved in regulating intracellular homeostasis. Transcription factor Forkhead box O1 (FoxO1) also regulates fundamental cellular processes, including cell differentiation, metabolism and apoptosis, and proliferation to cellular stress. Increasing evidence suggest that autophagy and FoxO1 are involved in the pathogenesis of T2DM, including β-cell viability, apoptosis, insulin secretion and peripheral insulin resistance. Recent studies have demonstrated that FoxO1 improves insulin resistance by regulating target tissue autophagy. The present review summarizes current literature on the role of autophagy and FoxO1 in T2DM. The participation of FoxO1 in the development and occurrence of T2DM via autophagy is also discussed.
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spelling pubmed-81206622021-05-17 Role of FoxO1 in regulating autophagy in type 2 diabetes mellitus (Review) Li, Xiudan Wan, Tingting Li, Yanbo Exp Ther Med Review Type 2 diabetes mellitus (T2DM) is a major chronic disease that is characterized by pancreatic β-cell dysfunction and insulin resistance. Autophagy is a highly conserved intracellular recycling pathway and is involved in regulating intracellular homeostasis. Transcription factor Forkhead box O1 (FoxO1) also regulates fundamental cellular processes, including cell differentiation, metabolism and apoptosis, and proliferation to cellular stress. Increasing evidence suggest that autophagy and FoxO1 are involved in the pathogenesis of T2DM, including β-cell viability, apoptosis, insulin secretion and peripheral insulin resistance. Recent studies have demonstrated that FoxO1 improves insulin resistance by regulating target tissue autophagy. The present review summarizes current literature on the role of autophagy and FoxO1 in T2DM. The participation of FoxO1 in the development and occurrence of T2DM via autophagy is also discussed. D.A. Spandidos 2021-07 2021-05-02 /pmc/articles/PMC8120662/ /pubmed/34007316 http://dx.doi.org/10.3892/etm.2021.10139 Text en Copyright: © Li et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , 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 Review
Li, Xiudan
Wan, Tingting
Li, Yanbo
Role of FoxO1 in regulating autophagy in type 2 diabetes mellitus (Review)
title Role of FoxO1 in regulating autophagy in type 2 diabetes mellitus (Review)
title_full Role of FoxO1 in regulating autophagy in type 2 diabetes mellitus (Review)
title_fullStr Role of FoxO1 in regulating autophagy in type 2 diabetes mellitus (Review)
title_full_unstemmed Role of FoxO1 in regulating autophagy in type 2 diabetes mellitus (Review)
title_short Role of FoxO1 in regulating autophagy in type 2 diabetes mellitus (Review)
title_sort role of foxo1 in regulating autophagy in type 2 diabetes mellitus (review)
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120662/
https://www.ncbi.nlm.nih.gov/pubmed/34007316
http://dx.doi.org/10.3892/etm.2021.10139
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