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Disrupting Insulin and IGF Receptor Function in Cancer
The insulin and insulin-like growth factor (IGF) system plays an important role in regulating normal cell proliferation and survival. However, the IGF system is also implicated in many malignancies, including breast cancer. Preclinical studies indicate several IGF blocking approaches, such as monocl...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827299/ https://www.ncbi.nlm.nih.gov/pubmed/33429867 http://dx.doi.org/10.3390/ijms22020555 |
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author | Cao, Jingran Yee, Douglas |
author_facet | Cao, Jingran Yee, Douglas |
author_sort | Cao, Jingran |
collection | PubMed |
description | The insulin and insulin-like growth factor (IGF) system plays an important role in regulating normal cell proliferation and survival. However, the IGF system is also implicated in many malignancies, including breast cancer. Preclinical studies indicate several IGF blocking approaches, such as monoclonal antibodies and tyrosine kinase inhibitors, have promising therapeutic potential for treating diseases. Uniformly, phase III clinical trials have not shown the benefit of blocking IGF signaling compared to standard of care arms. Clinical and laboratory data argue that targeting Type I IGF receptor (IGF1R) alone may be insufficient to disrupt this pathway as the insulin receptor (IR) may also be a relevant cancer target. Here, we review the well-studied role of the IGF system in regulating malignancies, the limitations on the current strategies of blocking the IGF system in cancer, and the potential future directions for targeting the IGF system. |
format | Online Article Text |
id | pubmed-7827299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78272992021-01-25 Disrupting Insulin and IGF Receptor Function in Cancer Cao, Jingran Yee, Douglas Int J Mol Sci Review The insulin and insulin-like growth factor (IGF) system plays an important role in regulating normal cell proliferation and survival. However, the IGF system is also implicated in many malignancies, including breast cancer. Preclinical studies indicate several IGF blocking approaches, such as monoclonal antibodies and tyrosine kinase inhibitors, have promising therapeutic potential for treating diseases. Uniformly, phase III clinical trials have not shown the benefit of blocking IGF signaling compared to standard of care arms. Clinical and laboratory data argue that targeting Type I IGF receptor (IGF1R) alone may be insufficient to disrupt this pathway as the insulin receptor (IR) may also be a relevant cancer target. Here, we review the well-studied role of the IGF system in regulating malignancies, the limitations on the current strategies of blocking the IGF system in cancer, and the potential future directions for targeting the IGF system. MDPI 2021-01-08 /pmc/articles/PMC7827299/ /pubmed/33429867 http://dx.doi.org/10.3390/ijms22020555 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Cao, Jingran Yee, Douglas Disrupting Insulin and IGF Receptor Function in Cancer |
title | Disrupting Insulin and IGF Receptor Function in Cancer |
title_full | Disrupting Insulin and IGF Receptor Function in Cancer |
title_fullStr | Disrupting Insulin and IGF Receptor Function in Cancer |
title_full_unstemmed | Disrupting Insulin and IGF Receptor Function in Cancer |
title_short | Disrupting Insulin and IGF Receptor Function in Cancer |
title_sort | disrupting insulin and igf receptor function in cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7827299/ https://www.ncbi.nlm.nih.gov/pubmed/33429867 http://dx.doi.org/10.3390/ijms22020555 |
work_keys_str_mv | AT caojingran disruptinginsulinandigfreceptorfunctionincancer AT yeedouglas disruptinginsulinandigfreceptorfunctionincancer |