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Targeting insulin-like growth factor pathways
Some cancer cells depend on the function of specific molecules for their growth, survival, and metastatic potential. Targeting of these critical molecules has arguably been the best therapy for cancer as demonstrated by the success of tamoxifen and trastuzumab in breast cancer. This review will eval...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361182/ https://www.ncbi.nlm.nih.gov/pubmed/16450000 http://dx.doi.org/10.1038/sj.bjc.6602963 |
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author | Yee, D |
author_facet | Yee, D |
author_sort | Yee, D |
collection | PubMed |
description | Some cancer cells depend on the function of specific molecules for their growth, survival, and metastatic potential. Targeting of these critical molecules has arguably been the best therapy for cancer as demonstrated by the success of tamoxifen and trastuzumab in breast cancer. This review will evaluate the type I IGF receptor (IGF-IR) as a potential target for cancer therapy. As new drugs come forward targeting this receptor system, several issues will need to be addressed in the early clinical trials using these agents. |
format | Text |
id | pubmed-2361182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23611822009-09-10 Targeting insulin-like growth factor pathways Yee, D Br J Cancer Minireview Some cancer cells depend on the function of specific molecules for their growth, survival, and metastatic potential. Targeting of these critical molecules has arguably been the best therapy for cancer as demonstrated by the success of tamoxifen and trastuzumab in breast cancer. This review will evaluate the type I IGF receptor (IGF-IR) as a potential target for cancer therapy. As new drugs come forward targeting this receptor system, several issues will need to be addressed in the early clinical trials using these agents. Nature Publishing Group 2006-02-27 2006-01-31 /pmc/articles/PMC2361182/ /pubmed/16450000 http://dx.doi.org/10.1038/sj.bjc.6602963 Text en Copyright © 2006 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Minireview Yee, D Targeting insulin-like growth factor pathways |
title | Targeting insulin-like growth factor pathways |
title_full | Targeting insulin-like growth factor pathways |
title_fullStr | Targeting insulin-like growth factor pathways |
title_full_unstemmed | Targeting insulin-like growth factor pathways |
title_short | Targeting insulin-like growth factor pathways |
title_sort | targeting insulin-like growth factor pathways |
topic | Minireview |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361182/ https://www.ncbi.nlm.nih.gov/pubmed/16450000 http://dx.doi.org/10.1038/sj.bjc.6602963 |
work_keys_str_mv | AT yeed targetinginsulinlikegrowthfactorpathways |