Levav-Cohen Yaara, Haupt Sue, Haupt Ygal
The Hebrew University Hadassah Medical School, Lautenberg Center for General and Tumor Immunology, Jerusalem, Israel.
Growth Factors. 2005 Sep;23(3):183-92. doi: 10.1080/08977190500196218.
Genetic and biochemical evidence have demonstrated a direct link between Mdm2 and cancer development. Elevated expression of Mdm2 is observed in a significant proportion of different types of cancer. The major contribution of Mdm2 to the development of cancer is through a tight inhibition of the activities and stability of the tumor suppressor p53. However, extensive studies over the past few years have identified p53-independent functions of Mdm2, in the regulation of several important cellular processes and multiple signaling pathways. The promotion of cell cycle progression by Mdm2 is mediated via p53 inhibition, and by regulating the pRb/E2F complex. Mdm2 is an important mediator of growth and survival signaling in the PI3K/Akt pathway, an activator of certain steroid hormone receptors, and an inhibitor of the TGF-beta growth restrictive pathway. Thus, the impact on these pathways by deregulated Mdm2, as often observed in cancer, can be oncogenic in a permissible environment. This renders Mdm2 as an important target for the development of anti-cancer drugs.
遗传学和生物化学证据已证明Mdm2与癌症发展之间存在直接联系。在相当比例的不同类型癌症中都观察到Mdm2表达升高。Mdm2对癌症发展的主要作用是通过紧密抑制肿瘤抑制因子p53的活性和稳定性。然而,过去几年的广泛研究已经确定了Mdm2在调节几个重要细胞过程和多个信号通路方面具有不依赖p53的功能。Mdm2对细胞周期进程的促进作用是通过抑制p53以及调节pRb/E2F复合物来介导的。Mdm2是PI3K/Akt途径中生长和存活信号的重要介质,是某些类固醇激素受体的激活剂,也是TGF-β生长限制途径的抑制剂。因此,如在癌症中经常观察到的那样,Mdm2失调对这些途径的影响在适宜环境中可能具有致癌性。这使得Mdm2成为抗癌药物开发的重要靶点。