Ren Hui, Zhao Liqun, Li Yikun, Yue Ping, Deng Xingming, Owonikoko Taofeek K, Chen Mingwei, Khuri Fadlo R, Sun Shi-Yong
Department of Respiration, First Affiliated Hospital of Medical College of Xi'an Jiaotong University, Xi'an, Shaanxi 710061, PR China.
Cancer Lett. 2013 Sep 28;338(2):229-38. doi: 10.1016/j.canlet.2013.03.032. Epub 2013 Apr 2.
This study focuses on determining whether and how the novel PI3 kinase inhibitor NVP-BKM120 (BKM120) induces apoptosis and enhances TRAIL-induced apoptosis in human lung cancer cells. We found that BKM120 reduced Mcl-1 levels across the tested cell lines along with induction of apoptosis and enhancement of TRAIL-induced apoptosis. Enforced expression of ectopic Mcl-1 significantly attenuated the effects of BKM120 alone or in combination with TRAIL on induction of apoptosis. Thus Mcl-1 downregulation contributes to BKM120-induced apoptosis or enhancement of TRAIL-induced apoptosis. Moreover, we have demonstrated that BMK120 decreases Mcl-1 levels through facilitating its degradation involving a GSK3/FBXW7-dependent mechanism.
本研究聚焦于确定新型PI3激酶抑制剂NVP-BKM120(BKM120)是否以及如何诱导人肺癌细胞凋亡并增强TRAIL诱导的凋亡。我们发现,BKM120降低了所有测试细胞系中的Mcl-1水平,同时诱导凋亡并增强TRAIL诱导的凋亡。异位Mcl-1的强制表达显著减弱了BKM120单独或与TRAIL联合诱导凋亡的作用。因此,Mcl-1下调有助于BKM120诱导的凋亡或增强TRAIL诱导的凋亡。此外,我们已证明BMK120通过促进其依赖GSK3/FBXW7机制的降解来降低Mcl-1水平。