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Targeting insulin-like growth factor axis in hepatocellular carcinoma

The insulin-like growth factor (IGF) axis contains ligands, receptors, substrates, and ligand binding proteins. The essential role of IGF axis in hepatocellular carcinoma (HCC) has been illustrated in HCC cell lines and in animal xenograft models. Preclinical evidence provides ample indication that...

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Detalles Bibliográficos
Autores principales: Wu, Jennifer, Zhu, Andrew X
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141798/
https://www.ncbi.nlm.nih.gov/pubmed/21729319
http://dx.doi.org/10.1186/1756-8722-4-30
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author Wu, Jennifer
Zhu, Andrew X
author_facet Wu, Jennifer
Zhu, Andrew X
author_sort Wu, Jennifer
collection PubMed
description The insulin-like growth factor (IGF) axis contains ligands, receptors, substrates, and ligand binding proteins. The essential role of IGF axis in hepatocellular carcinoma (HCC) has been illustrated in HCC cell lines and in animal xenograft models. Preclinical evidence provides ample indication that all four components of IGF axis are crucial in the carcinogenic and metastatic potential of HCC. Several strategies targeting this system including monoclonal antibodies against the IGF 1 receptor (IGF-1R) and small molecule inhibitors of the tyrosine kinase function of IGF-1R are under active investigation. This review describes the most up-to-date understanding of this complex axis in HCC, and provides relevant information on clinical trials targeting the IGF axis in HCC with a focus on anti-IGF-1R approach. IGF axis is increasingly recognized as one of the most relevant pathways in HCC and agents targeting this axis can potentially play an important role in the treatment of HCC.
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spelling pubmed-31417982011-07-23 Targeting insulin-like growth factor axis in hepatocellular carcinoma Wu, Jennifer Zhu, Andrew X J Hematol Oncol Review The insulin-like growth factor (IGF) axis contains ligands, receptors, substrates, and ligand binding proteins. The essential role of IGF axis in hepatocellular carcinoma (HCC) has been illustrated in HCC cell lines and in animal xenograft models. Preclinical evidence provides ample indication that all four components of IGF axis are crucial in the carcinogenic and metastatic potential of HCC. Several strategies targeting this system including monoclonal antibodies against the IGF 1 receptor (IGF-1R) and small molecule inhibitors of the tyrosine kinase function of IGF-1R are under active investigation. This review describes the most up-to-date understanding of this complex axis in HCC, and provides relevant information on clinical trials targeting the IGF axis in HCC with a focus on anti-IGF-1R approach. IGF axis is increasingly recognized as one of the most relevant pathways in HCC and agents targeting this axis can potentially play an important role in the treatment of HCC. BioMed Central 2011-07-05 /pmc/articles/PMC3141798/ /pubmed/21729319 http://dx.doi.org/10.1186/1756-8722-4-30 Text en Copyright ©2011 Wu and Zhu; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Wu, Jennifer
Zhu, Andrew X
Targeting insulin-like growth factor axis in hepatocellular carcinoma
title Targeting insulin-like growth factor axis in hepatocellular carcinoma
title_full Targeting insulin-like growth factor axis in hepatocellular carcinoma
title_fullStr Targeting insulin-like growth factor axis in hepatocellular carcinoma
title_full_unstemmed Targeting insulin-like growth factor axis in hepatocellular carcinoma
title_short Targeting insulin-like growth factor axis in hepatocellular carcinoma
title_sort targeting insulin-like growth factor axis in hepatocellular carcinoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141798/
https://www.ncbi.nlm.nih.gov/pubmed/21729319
http://dx.doi.org/10.1186/1756-8722-4-30
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