Anti-insulin-like growth factor strategies in breast cancer

被引:16
|
作者
Jerome, L
Shiry, L
Leyland-Jones, B
机构
[1] McGill Univ, Dept Oncol, Montreal, PQ H2W 1S6, Canada
[2] Insmed Inc, Richmond, VA USA
关键词
D O I
10.1053/j.seminoncol.2004.01.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The insulin-like growth factors (IGF-I and -II) are potent mitogens and survival factors for both normal and malignant breast cells. These effects are mediated primarily through the IGF-I receptor (IGF-IR), which is significantly overexpressed and highly activated in breast tumors. The IGF-binding proteins are competitive inhibitors of IGF/IGF-IR interaction, limiting cellular proliferation and survival. Higher serum IGF-I levels or an increased ratio of IGF-I to IGF binding protein-3 is associated with an increased risk of developing breast cancer. Hence, interest in the IGF system as a potential target for the development of novel antineoplastic therapies has ensued. Several strategies to interrupt IGF-IR signaling are currently being evaluated for the treatment of breast cancer, including suppression of IGF production, reduction of functional IGF-IR levels, neutralization of IGF action, and inhibition of IGF-IR activation. © 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:54 / 63
页数:10
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