Cancer Research UK Clinical Centre, Leeds Institute of Molecular Medicine, St James's University Hospital, Beckett Street, Leeds LS9 7TF, UK.
Cancer Metastasis Rev. 2009 Dec;28(3-4):305-16. doi: 10.1007/s10555-009-9198-3.
The phosphatidylinositol 3-kinase (PI3K) pathway is a critical signal transduction pathway that regulates multiple cellular functions. Aberrant activation of this pathway has been identified in a wide range of cancers. Several pathway components including AKT, PI3K and mTOR represent potential therapeutic targets and many small molecule inhibitors are in development or early clinical trials. The complex regulation of the pathway, together with the multiple mechanisms by which it can be activated, make this a highly challenging pathway to target. For successful inhibition, detailed molecular information on individual tumours will be required and it is already clear that different tumour types show distinct combinations of alterations. Recent results have identified alterations in pathway components PIK3CA, PTEN, AKT1 and TSC1 in bladder cancer, some of which are significantly related to tumour phenotype and clinical behaviour. Co-existence of alterations to several PI3K pathway genes in some bladder tumours indicates that these proteins may have functions that are not related solely to the known canonical pathway.
磷脂酰肌醇 3-激酶(PI3K)通路是一个关键的信号转导通路,调节多种细胞功能。该通路的异常激活已在多种癌症中被确定。该通路的几个组成部分,包括 AKT、PI3K 和 mTOR,代表潜在的治疗靶点,许多小分子抑制剂正在开发或处于早期临床试验阶段。该通路的复杂调节以及它可以被激活的多种机制,使得该通路成为一个极具挑战性的靶向治疗目标。为了成功抑制,需要对单个肿瘤进行详细的分子信息,而且已经很清楚,不同的肿瘤类型表现出不同的改变组合。最近的结果表明,膀胱癌中存在通路成分 PIK3CA、PTEN、AKT1 和 TSC1 的改变,其中一些与肿瘤表型和临床行为有显著关系。一些膀胱癌中几种 PI3K 通路基因的改变共存表明,这些蛋白可能具有与已知的经典通路无关的功能。