Liu Jie, Xu Yang, Xie Guobin, Geng Bingjie, Yang Renjing, Tian Wenjing, Chen Haifeng, Wang Guanghui
School of Pharmaceutical Sciences, Xiamen University, Xiamen 361102, China.
Int J Mol Sci. 2024 Dec 20;25(24):13670. doi: 10.3390/ijms252413670.
Jacaranone derived from , a traditional Chinese medicine used for centuries, has been documented to exhibit anti-inflammatory and antiproliferative properties in various tumor cell lines. However, the mechanism of action and relationship between inflammation and apoptosis induced by jacaranone remain inadequately elucidated. In this study, the targets of jacaranone and cancer were identified from various databases, while potential targets and pathways were predicted through the analysis of the protein-protein interactions (PPI) network and pathway enrichment. Through a comprehensive network pharmacology analysis and corroborating experimental findings, we revealed that jacaranone induces tumor cell death by fine-tuning the tumor necrosis factor receptor 1 (TNFR1) downstream signaling pathway. TNFR1 serves as a key node that assembles into complexes I and II, regulating pathways including the nuclear factor (NF)-κB signaling pathway and the cell apoptosis pathway, which play crucial roles in cellular life activities. Jacaranone successfully guides survival signaling pathways to apoptotic mechanisms by inhibiting the assembly of complex I and promoting the formation of complex II. In particular, the main action mechanism of jacaranone lies in inducing the degradation of the inhibitor of apoptosis protein (cIAP)-2. cIAP-2 serves as an E3 ubiquitin ligase that ubiquitinates receptor-interacting serine/threonine-protein kinase 1 (RIPK1), thereby hindering the formation of complex I and effectively reducing the phosphorylation of Inhibitor of κB kinase (IKK) β. When the deubiquitylation process of RIPK1 is triggered, it may promote the formation of complex II, which ultimately leads to cell apoptosis. This fully demonstrates the key role of jacaranone in regulating TNFR1 complexes, especially through the degradation of cIAP-2. Taken together, jacaranone hinders the assembly of TNFR1 complex I and promotes the formation of complex II to induce apoptosis of cancer cells. Our findings unveil a novel mechanism underlying jacaranone, while also presenting a fresh approach for the development of new pharmaceuticals.
鸦胆子酮源自一种已使用数百年的传统中药,文献记载其在多种肿瘤细胞系中具有抗炎和抗增殖特性。然而,鸦胆子酮诱导炎症和凋亡的作用机制及其之间的关系仍未得到充分阐明。在本研究中,从各种数据库中识别出鸦胆子酮和癌症的靶点,同时通过蛋白质 - 蛋白质相互作用(PPI)网络分析和通路富集预测潜在的靶点和通路。通过全面的网络药理学分析并结合实验结果,我们发现鸦胆子酮通过微调肿瘤坏死因子受体1(TNFR1)下游信号通路诱导肿瘤细胞死亡。TNFR1作为一个关键节点,组装成复合物I和II,调节包括核因子(NF)-κB信号通路和细胞凋亡通路在内的多种通路,这些通路在细胞生命活动中起关键作用。鸦胆子酮通过抑制复合物I的组装并促进复合物II的形成,成功地将生存信号通路导向凋亡机制。特别是,鸦胆子酮的主要作用机制在于诱导凋亡抑制蛋白(cIAP)-2的降解。cIAP-2作为一种E3泛素连接酶,使受体相互作用丝氨酸/苏氨酸蛋白激酶1(RIPK1)泛素化,从而阻碍复合物I的形成并有效降低κB激酶(IKK)β抑制剂的磷酸化。当RIPK1的去泛素化过程被触发时,它可能促进复合物II的形成,最终导致细胞凋亡。这充分证明了鸦胆子酮在调节TNFR1复合物中的关键作用,特别是通过cIAP-2的降解。综上所述,鸦胆子酮阻碍TNFR1复合物I的组装并促进复合物II的形成以诱导癌细胞凋亡。我们的研究结果揭示了鸦胆子酮的一种新机制,同时也为新型药物的开发提供了一种新方法。