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PPARγ and Apoptosis in Cancer

Peroxisome proliferator-activated receptors (PPARs) are ligand binding transcription factors which function in many physiological roles including lipid metabolism, cell growth, differentiation, and apoptosis. PPARs and their ligands have been shown to play a role in cancer. In particular, PPARγ liga...

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Detalles Bibliográficos
Autores principales: Elrod, Heath A., Sun, Shi-Yong
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442903/
https://www.ncbi.nlm.nih.gov/pubmed/18615184
http://dx.doi.org/10.1155/2008/704165
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author Elrod, Heath A.
Sun, Shi-Yong
author_facet Elrod, Heath A.
Sun, Shi-Yong
author_sort Elrod, Heath A.
collection PubMed
description Peroxisome proliferator-activated receptors (PPARs) are ligand binding transcription factors which function in many physiological roles including lipid metabolism, cell growth, differentiation, and apoptosis. PPARs and their ligands have been shown to play a role in cancer. In particular, PPARγ ligands including endogenous prostaglandins and the synthetic thiazolidinediones (TZDs) can induce apoptosis of cancer cells with antitumor activity. Thus, PPARγ ligands have a potential in both chemoprevention and therapy of several types of cancer either as single agents or in combination with other antitumor agents. Accordingly, the involvement of PPARγ and its ligands in regulation of apoptosis of cancer cells have been extensively studied. Depending on cell types or ligands, induction of apoptosis in cancer cells by PPARγ ligands can be either PPARγ-dependent or -independent. Through increasing our understanding of the mechanisms of PPARγ ligand-induced apoptosis, we can develop better strategies which may include combining other antitumor agents for PPARγ-targeted cancer chemoprevention and therapy. This review will highlight recent research advances on PPARγ and apoptosis in cancer.
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spelling pubmed-24429032008-07-09 PPARγ and Apoptosis in Cancer Elrod, Heath A. Sun, Shi-Yong PPAR Res Review Article Peroxisome proliferator-activated receptors (PPARs) are ligand binding transcription factors which function in many physiological roles including lipid metabolism, cell growth, differentiation, and apoptosis. PPARs and their ligands have been shown to play a role in cancer. In particular, PPARγ ligands including endogenous prostaglandins and the synthetic thiazolidinediones (TZDs) can induce apoptosis of cancer cells with antitumor activity. Thus, PPARγ ligands have a potential in both chemoprevention and therapy of several types of cancer either as single agents or in combination with other antitumor agents. Accordingly, the involvement of PPARγ and its ligands in regulation of apoptosis of cancer cells have been extensively studied. Depending on cell types or ligands, induction of apoptosis in cancer cells by PPARγ ligands can be either PPARγ-dependent or -independent. Through increasing our understanding of the mechanisms of PPARγ ligand-induced apoptosis, we can develop better strategies which may include combining other antitumor agents for PPARγ-targeted cancer chemoprevention and therapy. This review will highlight recent research advances on PPARγ and apoptosis in cancer. Hindawi Publishing Corporation 2008 2008-07-02 /pmc/articles/PMC2442903/ /pubmed/18615184 http://dx.doi.org/10.1155/2008/704165 Text en Copyright © 2008 H. A. Elrod and S.-Y. Sun. 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
Elrod, Heath A.
Sun, Shi-Yong
PPARγ and Apoptosis in Cancer
title PPARγ and Apoptosis in Cancer
title_full PPARγ and Apoptosis in Cancer
title_fullStr PPARγ and Apoptosis in Cancer
title_full_unstemmed PPARγ and Apoptosis in Cancer
title_short PPARγ and Apoptosis in Cancer
title_sort pparγ and apoptosis in cancer
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442903/
https://www.ncbi.nlm.nih.gov/pubmed/18615184
http://dx.doi.org/10.1155/2008/704165
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