Jiang Qi-Wei, Cheng Ke-Jun, Mei Xiao-Long, Qiu Jian-Ge, Zhang Wen-Ji, Xue You-Qiu, Qin Wu-Ming, Yang Yang, Zheng Di-Wei, Chen Yao, Wei Meng-Ning, Zhang Xu, Lv Min, Chen Mei-Wan, Wei Xing, Shi Zhi
Department of Cell Biology & Institute of Biomedicine, National Engineering Research Center of Genetic Medicine, Guangdong Provincial Key Laboratory of Bioengineering Medicine, College of Life Science and Technology, Jinan University, Guangzhou, Guangdong, China.
Chemical Biology Center, Lishui Institute of Agricultural Sciences, Lishui, Zhejiang, China.
Oncotarget. 2015 Oct 20;6(32):32790-804. doi: 10.18632/oncotarget.5411.
Triptolide and celastrol are two main active compounds isolated from Thunder God Vine with the potent anticancer activity. However, the anticancer effect of triptolide in combination with celastrol is still unknown. In the present study, we demonstrated that the combination of triptolide with celastrol synergistically induced cell growth inhibition, cell cycle arrest at G2/M phase and apoptosis with the increased intracellular ROS accumulation in cancer cells. Pretreatment with ROS scavenger N-acetyl-L-cysteine dramatically blocked the apoptosis induced by co-treatment with triptolide and celastrol. Treatment with celastrol alone led to the decreased expressions of HSP90 client proteins including survivin, AKT, EGFR, which was enhanced by the addition of triptolide. Additionally, the celastrol-induced expression of HSP70 and HSP27 was abrogated by triptolide. In the nude mice with xenograft tumors, the lower-dose combination of triptolide with celastrol significantly inhibited the growth of tumors without obvious toxicity. Overall, triptolide in combination with celastrol showed outstanding synergistic anticancer effect in vitro and in vivo, suggesting that this beneficial combination may offer a promising treatment option for cancer patients.
雷公藤甲素和雷公藤红素是从雷公藤中分离出的两种主要活性化合物,具有强大的抗癌活性。然而,雷公藤甲素与雷公藤红素联合使用的抗癌效果仍不清楚。在本研究中,我们证明雷公藤甲素与雷公藤红素联合使用可协同诱导癌细胞生长抑制、细胞周期阻滞于G2/M期以及细胞凋亡,并伴有癌细胞内活性氧积累增加。用活性氧清除剂N-乙酰-L-半胱氨酸预处理可显著阻断雷公藤甲素与雷公藤红素联合处理诱导的细胞凋亡。单独使用雷公藤红素处理导致包括生存素、AKT、表皮生长因子受体(EGFR)在内的热休克蛋白90(HSP90)客户蛋白表达降低,而添加雷公藤甲素可增强这种降低作用。此外,雷公藤甲素可消除雷公藤红素诱导的热休克蛋白70(HSP70)和热休克蛋白27(HSP27)的表达。在异种移植瘤裸鼠中,雷公藤甲素与雷公藤红素的低剂量联合使用可显著抑制肿瘤生长且无明显毒性。总体而言,雷公藤甲素与雷公藤红素联合使用在体外和体内均显示出显著的协同抗癌效果,表明这种有益的联合用药可能为癌症患者提供一种有前景的治疗选择。