Division of Hematology/Oncology, Department of Medicine, New York Medical College and Westchester Medical Center, Valhalla, NY 10595, USA.
J Hematol Oncol. 2013 Nov 22;6(1):88. doi: 10.1186/1756-8722-6-88.
Phosphatidylinositol 3-kinases (PI3Ks) are lipid kinases that regulate diverse cellular processes including proliferation, adhesion, survival, and motility. Dysregulated PI3K pathway signaling occurs in one-third of human tumors. Aberrantly activated PI3K signaling also confers sensitivity and resistance to conventional therapies. PI3K has been recognized as an attractive molecular target for novel anti-cancer molecules. In the last few years, several classes of potent and selective small molecule PI3K inhibitors have been developed, and at least fifteen compounds have progressed into clinical trials as new anticancer drugs. Among these, idelalisib has advanced to phase III trials in patients with advanced indolent non-Hodgkin's lymphoma and mantle cell lymphoma. In this review, we summarized the major molecules of PI3K signaling pathway, and discussed the preclinical models and clinical trials of potent small-molecule PI3K inhibitors.
磷脂酰肌醇 3-激酶(PI3Ks)是脂质激酶,可调节多种细胞过程,包括增殖、黏附、存活和运动。三分之一的人类肿瘤存在 PI3K 通路信号失调。异常激活的 PI3K 信号还会导致对常规治疗的敏感性和耐药性。PI3K 已被认为是新型抗癌分子有吸引力的分子靶标。在过去的几年中,已经开发出了几类有效的、选择性的小分子 PI3K 抑制剂,至少有十五种化合物作为新型抗癌药物已进入临床试验阶段。其中,idelalisib 已进入晚期惰性非霍奇金淋巴瘤和套细胞淋巴瘤患者的 III 期临床试验。在这篇综述中,我们总结了 PI3K 信号通路的主要分子,并讨论了有效的小分子 PI3K 抑制剂的临床前模型和临床试验。