Targeting the Type I Insulin-Like Growth Factor System for Breast Cancer Therapy

被引:15
|
作者
Sachdev, Deepali [1 ,2 ]
机构
[1] Univ Minnesota, Masonic Canc Ctr, Dept Med, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Masonic Canc Ctr, Dept Pharmacol, Minneapolis, MN 55455 USA
关键词
Breast cancer; targeted therapy; insulin-like growth factors; IGF-1R; antibodies; small molecule inhibitors; clinical trials; MONOCLONAL-ANTIBODY FIGITUMUMAB; FACTOR-RECEPTOR; IGF-I; TUMOR-GROWTH; ESTROGEN-RECEPTOR; PROSTATE-CANCER; PHASE-I; INSULIN-RECEPTOR-SUBSTRATE-1; IRS-1; ADJUVANT CHEMOTHERAPY; SIGNALING PATHWAYS;
D O I
10.2174/138945010792006816
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The insulin-like growth factors (IGFs) acting via the type I IGF receptor (IGF-1R) regulate cancer cell proliferation, survival, metabolism and metastasis. Drugs targeting the IGF-1R are being tested in human clinical trials for cancer therapy and it seems likely that this class of drugs could be approved soon. Recent data suggests that insulin receptor, which is closely related to IGF-1R, should also be targeted to maximally inhibit the system. Furthermore, biomarkers that identify patients whose tumors are driven by IGF-1R and biomarkers that allow monitoring or prediction of response are needed. This article reviews the different drugs against IGF-1R that are being tested and how this receptor pathway can be optimally targeted for cancer therapy with an emphasis on breast cancer therapy.
引用
收藏
页码:1121 / 1132
页数:12
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