| Literature DB >> 18508432 |
Angelo J Casa1, Robert K Dearth, Beate C Litzenburger, Adrian V Lee, Xiaojiang Cui.
Abstract
The insulin-like growth factor (IGF) ligands stimulate cellular proliferation and survival by activating the type I insulin-like growth factor receptor (IGF-IR). As a result, the IGF signaling system is implicated in a number of cancers, including those of the breast, prostate, and lung. In addition to mitogenic and anti-apoptotic roles that may directly influence tumor development, IGF-IR also appears to be a critical determinant of response to numerous cancer therapies. This review describes the role of the IGF-IR pathway in mediating resistance to both general cytotoxic therapies, such as radiation and chemotherapy, and targeted therapies, such as tamoxifen and trastuzumab. It concludes with a description of approaches to target IGF-IR and argues that inhibition of IGF signaling, in conjunction with standard therapies, may enhance the response of cancer cells to multiple modalities.Entities:
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Year: 2008 PMID: 18508432 DOI: 10.2741/2925
Source DB: PubMed Journal: Front Biosci ISSN: 1093-4715