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PPARα modulates gene expression profiles of mitochondrial energy metabolism in oral tumorigenesis

Metabolic reprogramming plays a crucial role in the development of cancer. The aim of this study was to explore the effect of fenofibrate, an agonist of peroxisome proliferator-activated receptor alpha (PPARα), on gene expression profiles of mitochondrial energy metabolism. Our results showed that P...

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Detalles Bibliográficos
Autores principales: Huang, Yi-Ping, Chang, Nai Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: China Medical University 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751096/
https://www.ncbi.nlm.nih.gov/pubmed/26869356
http://dx.doi.org/10.7603/s40681-016-0003-7
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author Huang, Yi-Ping
Chang, Nai Wen
author_facet Huang, Yi-Ping
Chang, Nai Wen
author_sort Huang, Yi-Ping
collection PubMed
description Metabolic reprogramming plays a crucial role in the development of cancer. The aim of this study was to explore the effect of fenofibrate, an agonist of peroxisome proliferator-activated receptor alpha (PPARα), on gene expression profiles of mitochondrial energy metabolism. Our results showed that PPARα expression was negatively correlated with tumor progression in an oral cancer mouse model. Activation of PPARα through fenofibrate suppressed migration of oral cancer cells. Differential protein profiling demonstrated that expressions of genes related to mitochondrial energy metabolism were either up-regulated (Atp5g3, Cyc1, Ndufa5, Ndufa10, and Sdhd) or down-regulated (Cox5b, Ndufa1, Ndufb7, and Uqcrh) through PPARα activation and response. Our results indicate that PPARα exhibits a great potential for anti-oral cancer therapies by modulating cancer cell mitochondrial energy metabolism.
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spelling pubmed-47510962016-02-22 PPARα modulates gene expression profiles of mitochondrial energy metabolism in oral tumorigenesis Huang, Yi-Ping Chang, Nai Wen Biomedicine (Taipei) Original Article Metabolic reprogramming plays a crucial role in the development of cancer. The aim of this study was to explore the effect of fenofibrate, an agonist of peroxisome proliferator-activated receptor alpha (PPARα), on gene expression profiles of mitochondrial energy metabolism. Our results showed that PPARα expression was negatively correlated with tumor progression in an oral cancer mouse model. Activation of PPARα through fenofibrate suppressed migration of oral cancer cells. Differential protein profiling demonstrated that expressions of genes related to mitochondrial energy metabolism were either up-regulated (Atp5g3, Cyc1, Ndufa5, Ndufa10, and Sdhd) or down-regulated (Cox5b, Ndufa1, Ndufb7, and Uqcrh) through PPARα activation and response. Our results indicate that PPARα exhibits a great potential for anti-oral cancer therapies by modulating cancer cell mitochondrial energy metabolism. China Medical University 2016-02-22 /pmc/articles/PMC4751096/ /pubmed/26869356 http://dx.doi.org/10.7603/s40681-016-0003-7 Text en © China Medical University 2016 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided original author(s) and source are credited.
spellingShingle Original Article
Huang, Yi-Ping
Chang, Nai Wen
PPARα modulates gene expression profiles of mitochondrial energy metabolism in oral tumorigenesis
title PPARα modulates gene expression profiles of mitochondrial energy metabolism in oral tumorigenesis
title_full PPARα modulates gene expression profiles of mitochondrial energy metabolism in oral tumorigenesis
title_fullStr PPARα modulates gene expression profiles of mitochondrial energy metabolism in oral tumorigenesis
title_full_unstemmed PPARα modulates gene expression profiles of mitochondrial energy metabolism in oral tumorigenesis
title_short PPARα modulates gene expression profiles of mitochondrial energy metabolism in oral tumorigenesis
title_sort pparα modulates gene expression profiles of mitochondrial energy metabolism in oral tumorigenesis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4751096/
https://www.ncbi.nlm.nih.gov/pubmed/26869356
http://dx.doi.org/10.7603/s40681-016-0003-7
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