Synergistic inhibitory effects of capsaicin combined with cisplatin on human osteosarcoma in culture and in xenografts

• Published in: Journal of experimental & clinical cancer research 2018-10, Vol.37 (1), p.251-17, Article 251
• Main Authors: Wang, Yang, Deng, Xu, Yu, Chang, Zhao, Guosheng, Zhou, Jing, Zhang, Ge, Li, Ming, Jiang, Dianming, Quan, Zhengxue, Zhang, Yuan
• Format: Article
• Language: English
• Subjects: Animals; Antineoplastic Combined Chemotherapy Protocols - pharmacology; Apoptosis; Autophagy; Autophagy - drug effects; Bone cancer; Bone Neoplasms - drug therapy; Bone Neoplasms - metabolism; Bone Neoplasms - pathology; Cancer; Cancer therapies; Capsaicin; Capsaicin - administration & dosage; Capsaicin - pharmacology; Cell cycle; Cell Line, Tumor; Chemotherapy; Cisplatin; Cisplatin - administration & dosage; Cisplatin - pharmacology; Combination therapy; Deoxyribonucleic acid; Diagnosis; DNA; Drug Synergism; Humans; Male; Medical prognosis; Metastasis; Mice; Mice, Nude; Osteosarcoma; Osteosarcoma - drug therapy; Osteosarcoma - metabolism; Osteosarcoma - pathology; Phytochemicals; Reactive oxygen species; Reactive Oxygen Species - metabolism; Sarcoma; Xenograft Model Antitumor Assays; Xenotransplantation
• ISSN: 1756-9966; 0392-9078; 1756-9966
• DOI: 10.1186/s13046-018-0922-0

The combination of phytochemicals with chemotherapy drugs is an emerging new strategy for cancer therapy to increase antitumor responses. The present study investigates the effect of the combination of capsaicin (CAP) with cisplatin (DDP) and the potential underlying anticancer mechanisms in osteosarcoma (OS) cells in vitro and in vivo. Cell viability assays and isobolographic analyses demonstrated that the combination of CAP and DDP showed synergistic cytotoxic effects on OS cells. We chose relatively low concentrations of CAP (100 μM) and DDP (16.7 μM) for subsequent experiments. Generally, the combination of CAP and DDP had significant effects on apoptosis induction, cell cycle arrest and cell invasion inhibition in OS cells compared with the individual-treatment groups and the control group. Moreover, cotreatment with CAP and DDP triggered prosurvival autophagy through reactive oxygen species (ROS)/JNK and p-AKT/mTOR signaling in OS cells. The combination regimen of CAP and DDP also inhibited tumor growth in an OS xenograft model. These results suggest that the combination of CAP and DDP has strong inhibitory effects on OS cells and identify CAP as a promising agent for supplementing standard chemotherapy and possible future targeted therapy in OS.