Werner H, Le Roith D
Department of Clinical Biochemistry, Sackler Faculty of Medicine, Tel-Aviv University, Israel.
Crit Rev Oncog. 1997;8(1):71-92. doi: 10.1615/critrevoncog.v8.i1.40.
The biological actions of the insulin-like growth factors IGF-I and IGF-II are mediated by their activation of the IGF-IR, a transmembrane tyrosine kinase linked to the ras-raf-MAPK cascade. Functional IGF-IRs are required for the cell to progress through the cell cycle. Most importantly, cells lacking this receptor cannot be transformed by any of a number of dominant oncogenes, a finding that proves that the presence of the IGF-IR is important for the development of a malignant phenotype. Consistent with this role, the IGF-IR displays a potent antiapoptotic effect, both in vitro and in vivo. Because of its key role in the transformation process, the IGF-IR is actively studied as a potential therapeutic target in different types of neoplastic growth.
胰岛素样生长因子IGF-I和IGF-II的生物学作用是通过激活IGF-IR介导的,IGF-IR是一种与ras-raf-MAPK级联相关的跨膜酪氨酸激酶。功能性IGF-IR是细胞在细胞周期中进展所必需的。最重要的是,缺乏这种受体的细胞不能被多种显性癌基因中的任何一种转化,这一发现证明IGF-IR的存在对恶性表型的发展很重要。与这一作用一致,IGF-IR在体外和体内均显示出强大的抗凋亡作用。由于其在转化过程中的关键作用,IGF-IR作为不同类型肿瘤生长的潜在治疗靶点正在被积极研究。