The type I insulin-like growth factor receptor pathway: a key player in cancer therapeutic resistance

被引:105
作者
Casa, Angelo J. [2 ,3 ]
Dearth, Robert K. [2 ,3 ]
Litzenburger, Beate C. [2 ,3 ]
Lee, Adrian V. [2 ,3 ]
Cui, Xiaojiang [1 ]
机构
[1] St Johns Hlth Ctr, Dept Mol Oncol, John Wayne Canc Inst, Santa Monica, CA 90404 USA
[2] Baylor Coll Med, Dept Med, Breast Ctr, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2008年 / 13卷
关键词
breast cancer; chemotherapy; EGFR; endocrine therapy; estrogen receptor; HER2; IGF; IGF-IR; radiation; targeted therapy; therapeutic resistance;
D O I
10.2741/2925
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:3273 / 3287
页数:15
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