Wang Panpan, Mak Victor Cy, Cheung Lydia Wt
School of Biomedical Sciences, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong SAR, China.
Genes Dis. 2022 Mar 23;10(1):199-211. doi: 10.1016/j.gendis.2022.03.002. eCollection 2023 Jan.
The insulin-like growth factor (IGF) axis plays important roles in cancer development and metastasis. The type 1 IGF receptor (IGF-1R) is a key member in the IGF axis and has long been recognized for its oncogenic role in multiple cancer lineages. Here we review the occurrence of IGF-1R aberrations and activation mechanisms in cancers, which justify the development of anti-IGF-1R therapies. We describe the therapeutic agents available for IGF-1R inhibition, with focuses on the recent or ongoing pre-clinical and clinical studies. These include antisense oligonucleotide, tyrosine kinase inhibitors and monoclonal antibodies which may be conjugated with cytotoxic drug. Remarkably, simultaneous targeting of IGF-1R and several other oncogenic vulnerabilities has shown early promise, highlighting the potential benefits of combination therapy. Further, we discuss the challenges in targeting IGF-1R so far and new concepts to improve therapeutic efficacy such as blockage of the nuclear translocation of IGF-1R.
胰岛素样生长因子(IGF)轴在癌症发展和转移中发挥着重要作用。1型IGF受体(IGF-1R)是IGF轴的关键成员,长期以来因其在多种癌症谱系中的致癌作用而受到认可。在此,我们综述了癌症中IGF-1R畸变的发生情况及其激活机制,这些为抗IGF-1R疗法的开发提供了依据。我们描述了可用于抑制IGF-1R的治疗药物,重点介绍了近期或正在进行的临床前和临床研究。这些药物包括反义寡核苷酸、酪氨酸激酶抑制剂以及可与细胞毒性药物偶联的单克隆抗体。值得注意的是,同时靶向IGF-1R和其他几种致癌弱点已显示出早期前景,突出了联合治疗的潜在益处。此外,我们讨论了迄今为止靶向IGF-1R所面临的挑战以及提高治疗效果的新概念,如阻断IGF-1R的核转位。