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HMGB1-dependent and -independent autophagy

HMGB1 (high mobility group box 1) is a multifunctional, ubiquitous protein located inside and outside cells that plays a critical role in various physiological and pathological processes including cell development, differentiation, inflammation, immunity, metastasis, metabolism, and death. Increasin...

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Detalles Bibliográficos
Autores principales: Sun, Xiaofang, Tang, Daolin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4198373/
https://www.ncbi.nlm.nih.gov/pubmed/25126737
http://dx.doi.org/10.4161/auto.32184
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author Sun, Xiaofang
Tang, Daolin
author_facet Sun, Xiaofang
Tang, Daolin
author_sort Sun, Xiaofang
collection PubMed
description HMGB1 (high mobility group box 1) is a multifunctional, ubiquitous protein located inside and outside cells that plays a critical role in various physiological and pathological processes including cell development, differentiation, inflammation, immunity, metastasis, metabolism, and death. Increasing evidence demonstrates that HMGB1-dependent autophagy promotes chemotherapy resistance, sustains tumor metabolism requirements and T cell survival, prevents polyglutamine aggregates and excitotoxicity, and protects against endotoxemia, bacterial infection, and ischemia-reperfusion injury in vitro or in vivo. In contrast, HMGB1 may not be required for autophagy in some organs such as the liver and heart. Understanding HMGB1-dependent and -independent autophagy in more detail will provide insight into the integrated stress response and guide HMGB1-based therapeutic intervention.
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spelling pubmed-41983732015-10-01 HMGB1-dependent and -independent autophagy Sun, Xiaofang Tang, Daolin Autophagy Views and Commentaries HMGB1 (high mobility group box 1) is a multifunctional, ubiquitous protein located inside and outside cells that plays a critical role in various physiological and pathological processes including cell development, differentiation, inflammation, immunity, metastasis, metabolism, and death. Increasing evidence demonstrates that HMGB1-dependent autophagy promotes chemotherapy resistance, sustains tumor metabolism requirements and T cell survival, prevents polyglutamine aggregates and excitotoxicity, and protects against endotoxemia, bacterial infection, and ischemia-reperfusion injury in vitro or in vivo. In contrast, HMGB1 may not be required for autophagy in some organs such as the liver and heart. Understanding HMGB1-dependent and -independent autophagy in more detail will provide insight into the integrated stress response and guide HMGB1-based therapeutic intervention. Landes Bioscience 2014-10-01 2014-08-13 /pmc/articles/PMC4198373/ /pubmed/25126737 http://dx.doi.org/10.4161/auto.32184 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by/3.0/ This is an open-access article licensed under a Creative Commons Attribution 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Views and Commentaries
Sun, Xiaofang
Tang, Daolin
HMGB1-dependent and -independent autophagy
title HMGB1-dependent and -independent autophagy
title_full HMGB1-dependent and -independent autophagy
title_fullStr HMGB1-dependent and -independent autophagy
title_full_unstemmed HMGB1-dependent and -independent autophagy
title_short HMGB1-dependent and -independent autophagy
title_sort hmgb1-dependent and -independent autophagy
topic Views and Commentaries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4198373/
https://www.ncbi.nlm.nih.gov/pubmed/25126737
http://dx.doi.org/10.4161/auto.32184
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