Massachusetts General Hospital Cancer Center, 149 13th St, Charlestown, 02129, USA.
J Clin Oncol. 2010 Feb 20;28(6):1075-83. doi: 10.1200/JCO.2009.25.3641. Epub 2010 Jan 19.
The phosphatidylinositol 3-kinase (PI3K) signaling axis impacts on cancer cell growth, survival, motility, and metabolism. This pathway is activated by several different mechanisms in cancers, including somatic mutation and amplification of genes encoding key components. In addition, PI3K signaling may serve integral functions for noncancerous cells in the tumor microenvironment. Consequently, therapeutics targeting the PI3K pathway are being developed at a rapid pace, and preclinical and early clinical studies are beginning to suggest specific strategies to effectively use them. However, the central role of PI3K signaling in a large array of diverse biologic processes raises concerns about its use in therapeutics and increases the need to develop sophisticated strategies for its use. In this review, we will discuss how PI3K signaling affects the growth and survival of tumor cells. From this vantage, we will consider how inhibitors of the PI3K signaling cascade, either alone or in combination with other therapeutics, can most effectively be used for the treatment of cancer.
磷脂酰肌醇 3-激酶(PI3K)信号通路影响癌细胞的生长、存活、运动和代谢。该通路在癌症中通过多种不同的机制激活,包括编码关键组成部分的基因的体细胞突变和扩增。此外,PI3K 信号通路可能为肿瘤微环境中的非癌细胞提供重要功能。因此,针对 PI3K 通路的治疗方法正在快速发展,临床前和早期临床研究开始提出有效使用它们的具体策略。然而,PI3K 信号在大量不同生物过程中的核心作用引起了人们对其在治疗中的应用的担忧,并增加了对其使用的复杂策略的需求。在这篇综述中,我们将讨论 PI3K 信号如何影响肿瘤细胞的生长和存活。从这个角度出发,我们将考虑如何单独使用或与其他治疗方法联合使用 PI3K 信号级联的抑制剂最有效地用于癌症治疗。