Key Laboratory of Industrial Microbiology, Ministry of Education, Tianjin Key Laboratory of Industry Microbiology, State Key Laboratory of Food Nutrition and Safety, National and Local United Engineering Lab of Metabolic Control Fermentation Technology, College of Biotechnology, Tianjin University of Science & Technology, Tianjin, China.
Tianjin Key Laboratory for Modern Drug Delivery and High Efficiency, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin, China.
Cell Prolif. 2019 Jan;52(1):e12520. doi: 10.1111/cpr.12520. Epub 2018 Oct 18.
Drug combination has a promising and potential development prospect in the treatment of various cancers. The objective of this study is to investigate the synergistic mechanisms of polyphyllin VII (PVII) and formosanin C (FC) in lung cancer.
The combination of FC and PVII influenced on the apoptosis, autophagy, and the relative signalling pathways were analysed in lung cancer cells.
The combination of FC and PVII demonstrated a concentration- dependent growth inhibition in human lung cancer cells. The combination index (CI) obtained from four lung cancer cells was smaller than 1. This synergistic antitumour effect was based on the increase of their single proapoptotic effect but inhibiting FC-induced autophagy in NCI-H460 cells. FC and PVII activated proapoptotic elements like cleaved-caspase-3, -8, and -9 to induce Beclin1 cleaved into Beclin1-C which suppressed FC-triggered autophagy and enhanced apoptosis.
Formosanin C and PVII showed a synergistic antitumour effect on lung cancer cells. The findings would provide the foundation for the use of combination drugs in the future.
药物联合治疗在各种癌症的治疗中具有广阔的发展前景。本研究旨在探讨重楼皂苷 VII(PVII)和重楼皂苷 C(FC)在肺癌中的协同作用机制。
分析 FC 和 PVII 联合作用对肺癌细胞凋亡、自噬及相关信号通路的影响。
FC 和 PVII 联合在人肺癌细胞中表现出浓度依赖性生长抑制。从四种肺癌细胞中获得的组合指数(CI)均小于 1。这种协同抗肿瘤作用基于其单一促凋亡作用的增加,但抑制了 NCI-H460 细胞中 FC 诱导的自噬。FC 和 PVII 激活了促凋亡因子,如 cleaved-caspase-3、-8 和 -9,诱导 Beclin1 裂解成 Beclin1-C,抑制 FC 触发的自噬并增强凋亡。
FC 和 PVII 对肺癌细胞表现出协同抗肿瘤作用。这些发现将为未来联合用药提供依据。