Department of Pharmacology, University of Minnesota, Minneapolis, MN 55455, USA.
Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA.
Int J Mol Sci. 2021 Jan 8;22(2):555. doi: 10.3390/ijms22020555.
The insulin and insulin-like growth factor (IGF) system plays an important role in regulating normal cell proliferation and survival. However, the IGF system is also implicated in many malignancies, including breast cancer. Preclinical studies indicate several IGF blocking approaches, such as monoclonal antibodies and tyrosine kinase inhibitors, have promising therapeutic potential for treating diseases. Uniformly, phase III clinical trials have not shown the benefit of blocking IGF signaling compared to standard of care arms. Clinical and laboratory data argue that targeting Type I IGF receptor (IGF1R) alone may be insufficient to disrupt this pathway as the insulin receptor (IR) may also be a relevant cancer target. Here, we review the well-studied role of the IGF system in regulating malignancies, the limitations on the current strategies of blocking the IGF system in cancer, and the potential future directions for targeting the IGF system.
胰岛素和胰岛素样生长因子(IGF)系统在调节正常细胞增殖和存活方面起着重要作用。然而,IGF 系统也与许多恶性肿瘤有关,包括乳腺癌。临床前研究表明,几种 IGF 阻断方法,如单克隆抗体和酪氨酸激酶抑制剂,具有治疗疾病的潜在治疗潜力。一致的是,III 期临床试验并未显示阻断 IGF 信号与标准治疗相比具有优势。临床和实验室数据表明,单独靶向 I 型 IGF 受体(IGF1R)可能不足以破坏该途径,因为胰岛素受体(IR)也可能是相关的癌症靶点。在这里,我们回顾了 IGF 系统在调节恶性肿瘤方面的研究进展,讨论了当前阻断 IGF 系统在癌症中应用的局限性,以及针对 IGF 系统的潜在未来方向。