Sun Xiao-Hong, Chai Yi-Hong, Bai Xiao-Teng, Li Hong-Xing, Yang Pan-Pan, Xi Ya-Ming
The First Clinical Medical College of Lanzhou University, Lanzhou, 730000, People's Republic of China.
Department of Gynecology and Obstetrics, The First Hospital of Lanzhou University, Lanzhou, 730000, People's Republic of China.
Drug Des Devel Ther. 2025 Mar 17;19:1983-2001. doi: 10.2147/DDDT.S498458. eCollection 2025.
This study aims to investigate the antitumor effects of saikosaponin A (SSA) on acute myeloid leukemia (AML) and elucidate its underlying mechanisms, particularly focusing on the endoplasmic reticulum stress (ERS)-mediated MAPK-p-JNK signaling pathway.
The inhibitory effects of SSA on the proliferation of AML cell lines K562 and HL60 were evaluated using CCK8 and EdU assays. Apoptotic effects induced by SSA were analyzed via flow cytometry. RNA sequencing was performed to identify differentially expressed genes and enriched signaling pathways. Western blot analysis was utilized to confirm the involvement of ERS and activation of the MAPK-p-JNK signaling pathway. Further validation of the potential mechanism of SSA-induced apoptosis was conducted using SP600125 and 4PBA. The in vivo anti-AML efficacy of SSA was assessed using a xenograft model.
SSA exhibited significant inhibitory effects on the proliferation of AML cell lines K562 and HL60, with IC50 values at 12, 24, and 48 hours demonstrating time- and dose-dependency (19.84 μM, 17.86 μM, and 15.38 μM for K562; 22.73 μM, 17.02 μM, and 15.25 μM for HL60, respectively). Western blot analysis demonstrated that SSA induces apoptosis in AML cells through the mitochondrial apoptotic pathway. Transcriptomic profiling and Western blot analyses confirmed that SSA activates the ERS-mediated p-JNK signaling pathway to induce apoptosis in AML, a process that can be reversed by the addition of 4PBA or SP600125. Furthermore, SSA significantly reduced tumor volume and weight in a NOD-SCID mouse xenograft model without causing notable toxicity to the liver, kidneys, lungs, or heart, while also activating the ERS and p-JNK signaling pathways in vivo.
SSA induces apoptosis in AML cells by activating the ERS-mediated p-JNK signaling pathway, exhibiting significant anti-AML effects both in vitro and in vivo, accompanied by a favorable safety profile.
本研究旨在探讨柴胡皂苷A(SSA)对急性髓系白血病(AML)的抗肿瘤作用,并阐明其潜在机制,尤其关注内质网应激(ERS)介导的丝裂原活化蛋白激酶-磷酸化c-Jun氨基末端激酶(MAPK-p-JNK)信号通路。
采用CCK8和EdU检测法评估SSA对AML细胞系K562和HL60增殖的抑制作用。通过流式细胞术分析SSA诱导的凋亡效应。进行RNA测序以鉴定差异表达基因和富集的信号通路。利用蛋白质免疫印迹分析来确认ERS的参与以及MAPK-p-JNK信号通路的激活。使用SP600125和4-苯基丁酸(4PBA)对SSA诱导凋亡的潜在机制进行进一步验证。采用异种移植模型评估SSA的体内抗AML疗效。
SSA对AML细胞系K562和HL60的增殖具有显著抑制作用,在12、24和48小时的半数抑制浓度(IC50)值显示出时间和剂量依赖性(K562分别为19.84 μM、17.86 μM和15.38 μM;HL60分别为22.73 μM、17.02 μM和15.25 μM)。蛋白质免疫印迹分析表明,SSA通过线粒体凋亡途径诱导AML细胞凋亡。转录组分析和蛋白质免疫印迹分析证实,SSA激活ERS介导的p-JNK信号通路以诱导AML细胞凋亡,添加4PBA或SP600125可逆转这一过程。此外,在NOD-SCID小鼠异种移植模型中,SSA显著降低了肿瘤体积和重量,且未对肝脏、肾脏、肺或心脏造成明显毒性,同时在体内也激活了ERS和p-JNK信号通路。
SSA通过激活ERS介导的p-JNK信号通路诱导AML细胞凋亡,在体外和体内均表现出显著的抗AML作用,且安全性良好。