Targeting the insulin-like growth factor-1 receptor in human cancer

被引:86
|
作者
Arcaro, Alexandre [1 ]
机构
[1] Univ Bern, Dept Clin Res, Div Pediat Hematol Oncol, CH-3004 Bern, Switzerland
来源
基金
瑞士国家科学基金会;
关键词
cancer; clinical trials; insulin-like growth factor; IGF-1; receptor; monoclonal antibody; tyrosine kinase inhibitor; IGF-BINDING PROTEIN-3; MONOCLONAL-ANTIBODY CP-751,871; ADVANCED SOLID TUMORS; KINASE INHIBITOR NVP-AEW541; MYELOID-LEUKEMIA CELLS; COLORECTAL-CANCER; PROSTATE-CANCER; PHASE-II; ANTITUMOR-ACTIVITY; FACTOR (IGF)-I;
D O I
10.3389/fphar.2013.00030
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The insulin-like growth factor (IGF) signaling system plays a crucial role in human cancer and the IGF-1 receptor (IGF-1R) is an attractive drug target against which a variety of novel anti-tumor agents are being developed. Deregulation of the IGF signaling pathway frequently occurs in human cancer and involves the establishment of autocrine loops comprising IGF-1 or IGF-2 and/or IGF-1R over-expression. Epidemiologic studies have documented a link between elevated IGF levels and the development of solid tumors, such as breast, colon, and prostate cancer. Anti-cancer strategies targeting the IGF signaling system involve two main approaches, namely neutralizing antibodies and small molecule inhibitors of the IGF-1R kinase activity. There are numerous reports describing anti-tumor activity of these agents in pre-clinical models of major human cancers. In addition, multiple clinical trials have started to evaluate the safety and efficacy of selected IGF-1R inhibitors, in combination with standard chemotherapeutic regimens or other targeted agents in cancer patients. In this mini review, I will discuss the role of the IGF signaling system in human cancer and the main strategies which have been so far evaluated to target the IGF-1R.
引用
收藏
页数:8
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