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Peroxisome Proliferator-Activated Receptors in Lung Cancer

Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors belonging to the nuclear hormone receptor superfamily. Their discovery in the 1990s provided insights into the cellular mechanisms involved in the control of energy homeostasis; the regulation of cell diff...

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Detalles Bibliográficos
Autores principales: Keshamouni, Venkateshwar G., Han, ShouWei, Roman, Jesse
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2220082/
https://www.ncbi.nlm.nih.gov/pubmed/18274632
http://dx.doi.org/10.1155/2007/90289
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author Keshamouni, Venkateshwar G.
Han, ShouWei
Roman, Jesse
author_facet Keshamouni, Venkateshwar G.
Han, ShouWei
Roman, Jesse
author_sort Keshamouni, Venkateshwar G.
collection PubMed
description Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors belonging to the nuclear hormone receptor superfamily. Their discovery in the 1990s provided insights into the cellular mechanisms involved in the control of energy homeostasis; the regulation of cell differentiation, proliferation, and apoptosis; and the modulation of important biological and pathological processes related to inflammation, among others. Since then, PPARs have become an exciting therapeutic target for several diseases. PPARs are expressed by many tumors including lung carcinoma cells, and their function has been linked to the process of carcinogenesis in lung. Consequently, intense research is being conducted in this area with the hope of discovering new PPAR-related therapeutic targets for the treatment of lung cancer. This review summarizes the research being conducted in this area and focuses on the mechanisms by which PPARs are believed to affect lung tumor cell biology.
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spelling pubmed-22200822008-02-14 Peroxisome Proliferator-Activated Receptors in Lung Cancer Keshamouni, Venkateshwar G. Han, ShouWei Roman, Jesse PPAR Res Review Article Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors belonging to the nuclear hormone receptor superfamily. Their discovery in the 1990s provided insights into the cellular mechanisms involved in the control of energy homeostasis; the regulation of cell differentiation, proliferation, and apoptosis; and the modulation of important biological and pathological processes related to inflammation, among others. Since then, PPARs have become an exciting therapeutic target for several diseases. PPARs are expressed by many tumors including lung carcinoma cells, and their function has been linked to the process of carcinogenesis in lung. Consequently, intense research is being conducted in this area with the hope of discovering new PPAR-related therapeutic targets for the treatment of lung cancer. This review summarizes the research being conducted in this area and focuses on the mechanisms by which PPARs are believed to affect lung tumor cell biology. Hindawi Publishing Corporation 2007 2007-11-25 /pmc/articles/PMC2220082/ /pubmed/18274632 http://dx.doi.org/10.1155/2007/90289 Text en Copyright © 2007 Venkateshwar G. Keshamouni 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
Keshamouni, Venkateshwar G.
Han, ShouWei
Roman, Jesse
Peroxisome Proliferator-Activated Receptors in Lung Cancer
title Peroxisome Proliferator-Activated Receptors in Lung Cancer
title_full Peroxisome Proliferator-Activated Receptors in Lung Cancer
title_fullStr Peroxisome Proliferator-Activated Receptors in Lung Cancer
title_full_unstemmed Peroxisome Proliferator-Activated Receptors in Lung Cancer
title_short Peroxisome Proliferator-Activated Receptors in Lung Cancer
title_sort peroxisome proliferator-activated receptors in lung cancer
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2220082/
https://www.ncbi.nlm.nih.gov/pubmed/18274632
http://dx.doi.org/10.1155/2007/90289
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