Molecular Concepts Research (MCR), Münster, Germany.
Diabetol Metab Syndr. 2011 Apr 1;3(1):5. doi: 10.1186/1758-5996-3-5.
Insulin is one of the major metabolic hormones regulating glucose homeostasis in the organism and a key growth factor for normal and neoplastic cells. Work conducted primarily over the past 3 decades has unravelled the presence of insulin in human breast cancer tissues and, more recently, in human non-small cell lung carcinomas (NSCLC). These findings have suggested that intracellular insulin is involved in the development of these highly prevalent human tumors. A potential mechanism for such involvement is insulin's binding and inactivation of the retinoblastoma tumor suppressor protein (RB) which in turn is likely controlled by insulin-degrading enzyme (IDE). This model and its supporting data are collectively covered in this survey in order to provide further insight into insulin-driven oncogenesis and its reversal through future anticancer therapeutics.
胰岛素是调节机体葡萄糖内稳态的主要代谢激素之一,也是正常和肿瘤细胞的关键生长因子。过去 30 年的主要研究工作揭示了胰岛素在人类乳腺癌组织中的存在,以及最近在人类非小细胞肺癌(NSCLC)中的存在。这些发现表明,细胞内胰岛素参与了这些高发性人类肿瘤的发生。这种参与的一个潜在机制是胰岛素结合并失活视网膜母细胞瘤肿瘤抑制蛋白(RB),而 RB 可能受胰岛素降解酶(IDE)的控制。本综述涵盖了这一模型及其支持数据,旨在为进一步了解胰岛素驱动的致癌作用及其通过未来的抗癌治疗逆转提供更多的见解。