Cheng Christine K, Fan Qi-Wen, Weiss William A
Department of Neurology, University of California, San Francisco, CA 94143, USA.
Brain Pathol. 2009 Jan;19(1):112-20. doi: 10.1111/j.1750-3639.2008.00233.x.
The PI3 kinase (PI3K) family plays a complex role in cell biology and metabolism. Signaling through the PI3Ks is frequently activated in many human cancers, including glioblastoma, because of gain-of-function mutations in PIK3CA or loss of PTEN. Experiments involving genetic mouse models and small molecule inhibitors have helped to elucidate the roles of the regulatory and catalytic subunits of PI3K in metabolism and cancer. Downstream of PI3K is Akt, a critical effector of growth, proliferation and survival. The suggested dependence of glioblastoma tumors on PI3K signaling implies that PI3K inhibitors should lead to effective killing of these cancer cells, but that has been shown not to be the case. The engagement of other survival pathways in response to PI3K inhibition prompts the need to develop combination therapies that promote cytotoxicity in cancer cells.
PI3激酶(PI3K)家族在细胞生物学和新陈代谢中发挥着复杂的作用。由于PIK3CA的功能获得性突变或PTEN的缺失,通过PI3K的信号传导在包括胶质母细胞瘤在内的许多人类癌症中经常被激活。涉及基因小鼠模型和小分子抑制剂的实验有助于阐明PI3K的调节亚基和催化亚基在新陈代谢和癌症中的作用。PI3K的下游是Akt,它是生长、增殖和存活的关键效应因子。胶质母细胞瘤肿瘤对PI3K信号传导的依赖性表明,PI3K抑制剂应该能够有效杀死这些癌细胞,但事实并非如此。其他存活途径对PI3K抑制的参与促使人们需要开发能够促进癌细胞细胞毒性的联合疗法。