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PPARγ: The Portrait of a Target Ally to Cancer Chemopreventive Agents

Peroxisome proliferator-activated receptor-gamma (PPARγ), one of three ligand-activated transcription factors named PPAR, has been identified as a molecular target for cancer chemopreventive agents. PPARγ was initially understood as a regulator of adipocyte differentiation and glucose homeostasis wh...

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Detalles Bibliográficos
Autores principales: Sainis, Ioannis, Vareli, Katerina, Karavasilis, Vasilios, Briasoulis, Evangelos
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2528242/
https://www.ncbi.nlm.nih.gov/pubmed/18779870
http://dx.doi.org/10.1155/2008/436489
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author Sainis, Ioannis
Vareli, Katerina
Karavasilis, Vasilios
Briasoulis, Evangelos
author_facet Sainis, Ioannis
Vareli, Katerina
Karavasilis, Vasilios
Briasoulis, Evangelos
author_sort Sainis, Ioannis
collection PubMed
description Peroxisome proliferator-activated receptor-gamma (PPARγ), one of three ligand-activated transcription factors named PPAR, has been identified as a molecular target for cancer chemopreventive agents. PPARγ was initially understood as a regulator of adipocyte differentiation and glucose homeostasis while later on, it became evident that it is also involved in cell differentiation, apoptosis, and angiogenesis, biological processes which are deregulated in cancer. It is now established that PPARγ ligands can induce cell differentiation and yield early antineoplastic effects in several tumor types. Moreover, several bioactive natural products with cancer protecting potential are shown to operate through activation of PPARγ. Overall, PPARγ appears to be a prevalent target ally to cancer chemopreventive agents and therefore pursuing research in this area is of great relevance.
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spelling pubmed-25282422008-09-08 PPARγ: The Portrait of a Target Ally to Cancer Chemopreventive Agents Sainis, Ioannis Vareli, Katerina Karavasilis, Vasilios Briasoulis, Evangelos PPAR Res Review Article Peroxisome proliferator-activated receptor-gamma (PPARγ), one of three ligand-activated transcription factors named PPAR, has been identified as a molecular target for cancer chemopreventive agents. PPARγ was initially understood as a regulator of adipocyte differentiation and glucose homeostasis while later on, it became evident that it is also involved in cell differentiation, apoptosis, and angiogenesis, biological processes which are deregulated in cancer. It is now established that PPARγ ligands can induce cell differentiation and yield early antineoplastic effects in several tumor types. Moreover, several bioactive natural products with cancer protecting potential are shown to operate through activation of PPARγ. Overall, PPARγ appears to be a prevalent target ally to cancer chemopreventive agents and therefore pursuing research in this area is of great relevance. Hindawi Publishing Corporation 2008 2008-09-03 /pmc/articles/PMC2528242/ /pubmed/18779870 http://dx.doi.org/10.1155/2008/436489 Text en Copyright © 2008 Ioannis Sainis et al. https://creativecommons.org/licenses/by/3.0/ 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
Sainis, Ioannis
Vareli, Katerina
Karavasilis, Vasilios
Briasoulis, Evangelos
PPARγ: The Portrait of a Target Ally to Cancer Chemopreventive Agents
title PPARγ: The Portrait of a Target Ally to Cancer Chemopreventive Agents
title_full PPARγ: The Portrait of a Target Ally to Cancer Chemopreventive Agents
title_fullStr PPARγ: The Portrait of a Target Ally to Cancer Chemopreventive Agents
title_full_unstemmed PPARγ: The Portrait of a Target Ally to Cancer Chemopreventive Agents
title_short PPARγ: The Portrait of a Target Ally to Cancer Chemopreventive Agents
title_sort pparγ: the portrait of a target ally to cancer chemopreventive agents
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2528242/
https://www.ncbi.nlm.nih.gov/pubmed/18779870
http://dx.doi.org/10.1155/2008/436489
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