Molecular Biotechnology Center, University of Turin Turin, Italy.
Front Oncol. 2013 May 8;3:108. doi: 10.3389/fonc.2013.00108. eCollection 2013.
The phosphatidylinositol 3-kinase (PI3K) signaling pathway regulates several cellular processes and it's one of the most frequently deregulated pathway in human tumors. Given its prominent role in cancer, there is great interest in the development of inhibitors able to target several members of PI3K signaling pathway in clinical trials. These drug candidates include PI3K inhibitors, both pan- and isoform-specific inhibitors, AKT, mTOR, and dual PI3K/mTOR inhibitors. As novel compounds progress into clinical trials, it's becoming urgent to identify and select patient population that most likely benefit from PI3K inhibition. In this review we will discuss individual PIK3CA mutations as predictors of sensitivity and resistance to targeted therapies, leading to use of novel PI3K/mTOR/AKT inhibitors to a more "personalized" treatment.
磷脂酰肌醇 3-激酶(PI3K)信号通路调节多种细胞过程,是人类肿瘤中最常失调的途径之一。鉴于其在癌症中的重要作用,人们非常关注能够在临床试验中靶向多种 PI3K 信号通路成员的抑制剂的开发。这些候选药物包括 PI3K 抑制剂,包括 pan 和同工型特异性抑制剂、AKT、mTOR 和双重 PI3K/mTOR 抑制剂。随着新型化合物进入临床试验,迫切需要确定和选择最有可能从 PI3K 抑制中受益的患者人群。在这篇综述中,我们将讨论个体 PIK3CA 突变作为预测对靶向治疗的敏感性和耐药性的标志物,导致使用新型 PI3K/mTOR/AKT 抑制剂进行更“个体化”的治疗。