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Transcriptional Regulation of Fibroblast Growth Factor 21 Expression

Fibroblast growth factor 21 (FGF21) is an attractive target for treating metabolic disease due to its wide-ranging beneficial effects on glucose and lipid metabolism. Circulating FGF21 levels are increased in insulin-resistant states; however, endogenous FGF21 fails to improve glucose and lipid meta...

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Autores principales: Bae, Kwi-Hyun, Kim, Jung-Guk, Park, Keun-Gyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Endocrine Society 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091486/
https://www.ncbi.nlm.nih.gov/pubmed/25031882
http://dx.doi.org/10.3803/EnM.2014.29.2.105
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author Bae, Kwi-Hyun
Kim, Jung-Guk
Park, Keun-Gyu
author_facet Bae, Kwi-Hyun
Kim, Jung-Guk
Park, Keun-Gyu
author_sort Bae, Kwi-Hyun
collection PubMed
description Fibroblast growth factor 21 (FGF21) is an attractive target for treating metabolic disease due to its wide-ranging beneficial effects on glucose and lipid metabolism. Circulating FGF21 levels are increased in insulin-resistant states; however, endogenous FGF21 fails to improve glucose and lipid metabolism in obesity, suggesting that metabolic syndrome is an FGF21-resistant state. Therefore, transcription factors for FGF21 are potential drug targets that could increase FGF21 expression in obesity and reduce FGF21 resistance. Despite many studies on the metabolic effects of FGF21, the transcriptional regulation of FGF21 gene expression remains controversial and is not fully understood. As the FGF21 transcription factor pathway is one of the most promising targets for the treatment of metabolic syndrome, further investigation of FGF21 transcriptional regulation is required.
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spelling pubmed-40914862014-07-16 Transcriptional Regulation of Fibroblast Growth Factor 21 Expression Bae, Kwi-Hyun Kim, Jung-Guk Park, Keun-Gyu Endocrinol Metab (Seoul) Review Article Fibroblast growth factor 21 (FGF21) is an attractive target for treating metabolic disease due to its wide-ranging beneficial effects on glucose and lipid metabolism. Circulating FGF21 levels are increased in insulin-resistant states; however, endogenous FGF21 fails to improve glucose and lipid metabolism in obesity, suggesting that metabolic syndrome is an FGF21-resistant state. Therefore, transcription factors for FGF21 are potential drug targets that could increase FGF21 expression in obesity and reduce FGF21 resistance. Despite many studies on the metabolic effects of FGF21, the transcriptional regulation of FGF21 gene expression remains controversial and is not fully understood. As the FGF21 transcription factor pathway is one of the most promising targets for the treatment of metabolic syndrome, further investigation of FGF21 transcriptional regulation is required. Korean Endocrine Society 2014-06 2014-06-26 /pmc/articles/PMC4091486/ /pubmed/25031882 http://dx.doi.org/10.3803/EnM.2014.29.2.105 Text en Copyright © 2014 Korean Endocrine Society http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Bae, Kwi-Hyun
Kim, Jung-Guk
Park, Keun-Gyu
Transcriptional Regulation of Fibroblast Growth Factor 21 Expression
title Transcriptional Regulation of Fibroblast Growth Factor 21 Expression
title_full Transcriptional Regulation of Fibroblast Growth Factor 21 Expression
title_fullStr Transcriptional Regulation of Fibroblast Growth Factor 21 Expression
title_full_unstemmed Transcriptional Regulation of Fibroblast Growth Factor 21 Expression
title_short Transcriptional Regulation of Fibroblast Growth Factor 21 Expression
title_sort transcriptional regulation of fibroblast growth factor 21 expression
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091486/
https://www.ncbi.nlm.nih.gov/pubmed/25031882
http://dx.doi.org/10.3803/EnM.2014.29.2.105
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