Beijing Institute of Pharmacology and Toxicology, State Key Laboratory of Toxicology and Medical Countermeasures, Beijing, 100850, China.
State Key Laboratory of Functions and Applications of Medicinal Plants, Guizhou Medical University, Guiyang, 550014, China.
Acta Pharmacol Sin. 2019 Nov;40(11):1466-1479. doi: 10.1038/s41401-019-0253-5. Epub 2019 Jul 17.
Recently, inhibitor of apoptosis proteins (IAPs) and some IAP antagonists were found to regulate autophagy, but the underlying mechanisms remain unclear. WX20120108 is an analogue of GDC-0152 (a known IAP antagonist) and displays more potent anti-tumor and autophagy-regulating activity in tumor cells, we investigated the regulatory mechanisms underlying WX20120108-induced autophagy. Using molecular docking and fluorescence polarization anisotropy (FPA) competitive assay, we first demonstrated that WX20120108, acting as an IAP antagonist, bound to the XIAP-BIR3, XIAP BIR2-BIR3, cIAP1 BIR3, and cIAP2 BIR3 domains with high affinities. In six cancer cell lines, WX20120108 inhibited the cell proliferation with potencies two to ten-fold higher than that of GDC-0152. In HeLa and MDA-MB-231 cells, WX20120108 induced caspase-dependent apoptosis and activated TNFα-dependent extrinsic apoptosis. On the other hand, WX20120108 induced autophagy in HeLa and MDA-MB-231 cells in dose- and time-dependent manners. We revealed that WX20120108 selectively activated Foxo3, evidenced by Foxo3 nuclear translocation in both gene modified cell line and HeLa cells, as well as the upregulated expression of Foxo3-targeted genes (Bnip3, Pik3c3, Atg5, and Atg4b), which played a key role in autophagy initiation. WX20120108-induced autophagy was significantly suppressed when Foxo3 gene was silenced. WX20120108 dose-dependently increased the generation of reactive oxygen species (ROS) in HeLa cells, and WX20120108-induced Foxo3 activation was completely blocked in the presence of catalase, a known ROS scavenger. However, WX20120108-induced ROS generation was not affected by cIAP1/2 or XIAP gene silencing. In conclusion, WX20120108-induced autophagy relies on activating ROS-Foxo3 pathway, which is independent of IAPs. This finding provides a new insight into the mechanism of IAP antagonist-mediated regulation of autophagy.
最近发现凋亡抑制蛋白(IAPs)及其拮抗剂可以调节自噬,但具体机制尚不清楚。WX20120108 是 GDC-0152(已知的 IAP 拮抗剂)的类似物,在肿瘤细胞中显示出更强的抗肿瘤和自噬调节活性,我们研究了 WX20120108 诱导自噬的调控机制。通过分子对接和荧光偏振各向异性(FPA)竞争性测定,我们首先证明 WX20120108 作为 IAP 拮抗剂,与 XIAP-BIR3、XIAP BIR2-BIR3、cIAP1 BIR3 和 cIAP2 BIR3 结构域具有高亲和力。在六种癌细胞系中,WX20120108 抑制细胞增殖的活性比 GDC-0152 高 2 到 10 倍。在 HeLa 和 MDA-MB-231 细胞中,WX20120108 诱导 caspase 依赖性细胞凋亡和 TNFα 依赖性细胞外凋亡。另一方面,WX20120108 以剂量和时间依赖的方式诱导 HeLa 和 MDA-MB-231 细胞自噬。我们揭示了 WX20120108 选择性激活 Foxo3,这一点在基因修饰细胞系和 HeLa 细胞中 Foxo3 的核易位以及 Foxo3 靶向基因(Bnip3、Pik3c3、Atg5 和 Atg4b)的上调表达中得到了证明,这些基因在自噬起始中起着关键作用。当 Foxo3 基因沉默时,WX20120108 诱导的自噬显著受到抑制。WX20120108 呈剂量依赖性增加 HeLa 细胞中活性氧(ROS)的产生,并且在存在已知 ROS 清除剂过氧化氢酶的情况下,WX20120108 诱导的 Foxo3 激活完全被阻断。然而,WX20120108 诱导的 ROS 生成不受 cIAP1/2 或 XIAP 基因沉默的影响。总之,WX20120108 诱导的自噬依赖于激活 ROS-Foxo3 途径,该途径独立于 IAPs。这一发现为 IAP 拮抗剂介导的自噬调控机制提供了新的见解。