Université de Nice, Institut de Biologie Valrose, CNRS UMR 7277, INSERM UMR 1091, Nice, France.
Department of Biostatistics, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Cancer Lett. 2014 Nov 28;354(2):355-64. doi: 10.1016/j.canlet.2014.08.038. Epub 2014 Sep 6.
Fas and PI3K/Akt signaling pathways pivotally impact on cancer cell death and survival respectively and are considered as promising targets for innovative anticancer therapies. To better characterize the combination effect of PI3K/Akt inhibitors and Fas agonists and understand the profile of the interaction between PI3K/Akt and Fas signaling, we qualitatively and quantitatively evaluated the combination effect of PI3K/Akt inhibitors LY294002, Akt inhibitor VIII and FasL. At the concentration that can block cell cycle progression and DNA synthesis but not elicit apoptosis, these inhibitors potentiate FasL to induce apoptosis. At higher concentrations, when the PI3K/Akt inhibitors induce apoptosis, they synergize FasL to induce apoptosis. In addition, PI3K/Akt inhibition significantly facilitates the Fas-mediated apoptotic signaling. Understanding the combination effects between PI3K/Akt inhibition and Fas activation not only leads to rational design of effective combination therapy of PI3K/Akt inhibitors but also improve our knowledge about the impact of PI3K-Akt pathway on Fas signaling and the potential modulation of innate immune system by PI3K-Akt-targeting drugs in anticancer treatment.
Fas 和 PI3K/Akt 信号通路分别对癌细胞的死亡和存活起着关键作用,被认为是创新抗癌治疗的有前途的靶点。为了更好地描述 PI3K/Akt 抑制剂和 Fas 激动剂的联合作用,并了解 PI3K/Akt 和 Fas 信号之间的相互作用情况,我们定性和定量评估了 PI3K/Akt 抑制剂 LY294002、Akt 抑制剂 VIII 和 FasL 的联合作用。在能够阻断细胞周期进程和 DNA 合成但不会引发细胞凋亡的浓度下,这些抑制剂增强了 FasL 诱导细胞凋亡的能力。在更高的浓度下,当 PI3K/Akt 抑制剂诱导细胞凋亡时,它们与 FasL 协同诱导细胞凋亡。此外,PI3K/Akt 抑制显著促进 Fas 介导的凋亡信号。了解 PI3K/Akt 抑制与 Fas 激活之间的联合作用不仅可以合理设计有效的 PI3K/Akt 抑制剂联合治疗方案,还可以提高我们对 PI3K-Akt 通路对 Fas 信号的影响以及 PI3K-Akt 靶向药物在癌症治疗中对固有免疫系统的潜在调节作用的认识。