Suppr超能文献

基于 caspase 介导的 Beclin1 切割抑制自噬并促进凋亡,福司曲星 C 和重楼皂苷 VII 的协同抗癌作用。

The synergistic anticancer effect of formosanin C and polyphyllin VII based on caspase-mediated cleavage of Beclin1 inhibiting autophagy and promoting apoptosis.

机构信息

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.

出版信息

Cell Prolif. 2019 Jan;52(1):e12520. doi: 10.1111/cpr.12520. Epub 2018 Oct 18.

Abstract

OBJECTIVES

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.

MATERIALS AND METHODS

The combination of FC and PVII influenced on the apoptosis, autophagy, and the relative signalling pathways were analysed in lung cancer cells.

RESULTS

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.

CONCLUSIONS

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.

摘要

目的

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。

材料与方法

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。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/000c/6430456/5e216e75e161/CPR-52-e12520-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验