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PPAR Ligands Function as Suppressors That Target Biological Actions of HMGB1

High mobility group box 1 (HMGB1), which has become one of the most intriguing molecules in inflammatory disorders and cancers and with which ligand-activated peroxisome proliferator-activated receptors (PPARs) are highly associated, is considered as a therapeutic target. Of particular interest is t...

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Detalles Bibliográficos
Autores principales: Ying, Shibo, Xiao, Xiang, Chen, Tianhui, Lou, Jianlin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985574/
https://www.ncbi.nlm.nih.gov/pubmed/27563308
http://dx.doi.org/10.1155/2016/2612743
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author Ying, Shibo
Xiao, Xiang
Chen, Tianhui
Lou, Jianlin
author_facet Ying, Shibo
Xiao, Xiang
Chen, Tianhui
Lou, Jianlin
author_sort Ying, Shibo
collection PubMed
description High mobility group box 1 (HMGB1), which has become one of the most intriguing molecules in inflammatory disorders and cancers and with which ligand-activated peroxisome proliferator-activated receptors (PPARs) are highly associated, is considered as a therapeutic target. Of particular interest is the fact that certain PPAR ligands have demonstrated their potent anti-inflammatory activities and potential anticancer effects. In this review article we summarize recent experimental evidence that PPAR ligands function as suppressors that target biological actions of HMGB1, including intracellular expression, receptor signaling cascades, and extracellular secretion of HMGB1 in cell lines and/or animal models. We also propose the possible mechanisms underlying PPAR involvement in inflammatory disorders and discuss the future therapeutic value of PPAR ligands targeting HMGB1 molecule for cancer prevention and treatment.
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spelling pubmed-49855742016-08-25 PPAR Ligands Function as Suppressors That Target Biological Actions of HMGB1 Ying, Shibo Xiao, Xiang Chen, Tianhui Lou, Jianlin PPAR Res Review Article High mobility group box 1 (HMGB1), which has become one of the most intriguing molecules in inflammatory disorders and cancers and with which ligand-activated peroxisome proliferator-activated receptors (PPARs) are highly associated, is considered as a therapeutic target. Of particular interest is the fact that certain PPAR ligands have demonstrated their potent anti-inflammatory activities and potential anticancer effects. In this review article we summarize recent experimental evidence that PPAR ligands function as suppressors that target biological actions of HMGB1, including intracellular expression, receptor signaling cascades, and extracellular secretion of HMGB1 in cell lines and/or animal models. We also propose the possible mechanisms underlying PPAR involvement in inflammatory disorders and discuss the future therapeutic value of PPAR ligands targeting HMGB1 molecule for cancer prevention and treatment. Hindawi Publishing Corporation 2016 2016-08-02 /pmc/articles/PMC4985574/ /pubmed/27563308 http://dx.doi.org/10.1155/2016/2612743 Text en Copyright © 2016 Shibo Ying et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Ying, Shibo
Xiao, Xiang
Chen, Tianhui
Lou, Jianlin
PPAR Ligands Function as Suppressors That Target Biological Actions of HMGB1
title PPAR Ligands Function as Suppressors That Target Biological Actions of HMGB1
title_full PPAR Ligands Function as Suppressors That Target Biological Actions of HMGB1
title_fullStr PPAR Ligands Function as Suppressors That Target Biological Actions of HMGB1
title_full_unstemmed PPAR Ligands Function as Suppressors That Target Biological Actions of HMGB1
title_short PPAR Ligands Function as Suppressors That Target Biological Actions of HMGB1
title_sort ppar ligands function as suppressors that target biological actions of hmgb1
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985574/
https://www.ncbi.nlm.nih.gov/pubmed/27563308
http://dx.doi.org/10.1155/2016/2612743
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