Sheppard Karen, Kinross Kathryn M, Solomon Benjamin, Pearson Richard B, Phillips Wayne A
Division of Cancer Research, Peter MacCallum Cancer Centre, Department of Biochemistry and Molecular Biology, Monash University, Clayton, Australia.
Crit Rev Oncog. 2012;17(1):69-95. doi: 10.1615/critrevoncog.v17.i1.60.
The phosphatidylinositol 3 kinase (PI3K) pathway is one of the major pathways modulating cell growth, proliferation, metabolism, survival, and angiogenesis. Hyperactivation of this pathway is one of the most frequent occurrences in human cancer and is thus an obvious target for treatment of this disease. Currently there are 26 novel compounds targeting the PI3K pathway being assessed in more than 150 cancer-related clinical trials. Although this pathway is involved in many vital biologic functions, data emanating from these clinical trials indicate that these drugs are well tolerated. This review outlines the interaction of the PI3K pathway with other signaling cascades, highlights mechanisms involved in hyperactivation, discusses current therapeutics in cancer-related clinical trials that target this pathway, and, based on preclinical data, discusses possible leads on patient selection and combinational therapy, including targeting multiple components of the associated signaling network.
磷脂酰肌醇3激酶(PI3K)信号通路是调控细胞生长、增殖、代谢、存活及血管生成的主要信号通路之一。该信号通路的过度激活是人类癌症中最常见的现象之一,因此是治疗该疾病的一个明确靶点。目前,有26种靶向PI3K信号通路的新型化合物正在150多项癌症相关临床试验中进行评估。尽管该信号通路参与许多重要的生物学功能,但这些临床试验的数据表明,这些药物耐受性良好。本文综述了PI3K信号通路与其他信号级联的相互作用,强调了过度激活所涉及的机制,讨论了癌症相关临床试验中针对该信号通路的现有疗法,并根据临床前数据,探讨了患者选择和联合治疗的可能线索,包括靶向相关信号网络的多个组成部分。