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Recent Insights into Insulin-Like Growth Factor Binding Protein 2 Transcriptional Regulation

Insulin-like growth factor binding proteins (IGFBPs) are major regulators of insulin-like growth factor bioavailability and activity in metabolic signaling. Seven IGFBP family isoforms have been identified. Recent studies have shown that IGFBPs play a pivotal role in metabolic signaling and disease,...

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Detalles Bibliográficos
Autores principales: Shin, Minsang, Kang, Hye Suk, Park, Jae-Hyung, Bae, Jae-Hoon, Song, Dae-Kyu, Im, Seung-Soon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Endocrine Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368109/
https://www.ncbi.nlm.nih.gov/pubmed/28116872
http://dx.doi.org/10.3803/EnM.2017.32.1.11
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author Shin, Minsang
Kang, Hye Suk
Park, Jae-Hyung
Bae, Jae-Hoon
Song, Dae-Kyu
Im, Seung-Soon
author_facet Shin, Minsang
Kang, Hye Suk
Park, Jae-Hyung
Bae, Jae-Hoon
Song, Dae-Kyu
Im, Seung-Soon
author_sort Shin, Minsang
collection PubMed
description Insulin-like growth factor binding proteins (IGFBPs) are major regulators of insulin-like growth factor bioavailability and activity in metabolic signaling. Seven IGFBP family isoforms have been identified. Recent studies have shown that IGFBPs play a pivotal role in metabolic signaling and disease, including the pathogenesis of obesity, diabetes, and cancer. Although many studies have documented the various roles played by IGFBPs, transcriptional regulation of IGFBPs is not well understood. In this review, we focus on the regulatory mechanisms of IGFBP gene expression, and we summarize the findings of transcription factor activity in the IGFBP promoter region.
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spelling pubmed-53681092017-03-28 Recent Insights into Insulin-Like Growth Factor Binding Protein 2 Transcriptional Regulation Shin, Minsang Kang, Hye Suk Park, Jae-Hyung Bae, Jae-Hoon Song, Dae-Kyu Im, Seung-Soon Endocrinol Metab (Seoul) Review Article Insulin-like growth factor binding proteins (IGFBPs) are major regulators of insulin-like growth factor bioavailability and activity in metabolic signaling. Seven IGFBP family isoforms have been identified. Recent studies have shown that IGFBPs play a pivotal role in metabolic signaling and disease, including the pathogenesis of obesity, diabetes, and cancer. Although many studies have documented the various roles played by IGFBPs, transcriptional regulation of IGFBPs is not well understood. In this review, we focus on the regulatory mechanisms of IGFBP gene expression, and we summarize the findings of transcription factor activity in the IGFBP promoter region. Korean Endocrine Society 2017-03 2017-01-19 /pmc/articles/PMC5368109/ /pubmed/28116872 http://dx.doi.org/10.3803/EnM.2017.32.1.11 Text en Copyright © 2017 Korean Endocrine Society http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Shin, Minsang
Kang, Hye Suk
Park, Jae-Hyung
Bae, Jae-Hoon
Song, Dae-Kyu
Im, Seung-Soon
Recent Insights into Insulin-Like Growth Factor Binding Protein 2 Transcriptional Regulation
title Recent Insights into Insulin-Like Growth Factor Binding Protein 2 Transcriptional Regulation
title_full Recent Insights into Insulin-Like Growth Factor Binding Protein 2 Transcriptional Regulation
title_fullStr Recent Insights into Insulin-Like Growth Factor Binding Protein 2 Transcriptional Regulation
title_full_unstemmed Recent Insights into Insulin-Like Growth Factor Binding Protein 2 Transcriptional Regulation
title_short Recent Insights into Insulin-Like Growth Factor Binding Protein 2 Transcriptional Regulation
title_sort recent insights into insulin-like growth factor binding protein 2 transcriptional regulation
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368109/
https://www.ncbi.nlm.nih.gov/pubmed/28116872
http://dx.doi.org/10.3803/EnM.2017.32.1.11
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