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Synergistic inhibitory effects of capsaicin combined with cisplatin on human osteosarcoma in culture and in xenografts
BACKGROUND: The combination of phytochemicals with chemotherapy drugs is an emerging new strategy for cancer therapy to increase antitumor responses. METHODS: The present study investigates the effect of the combination of capsaicin (CAP) with cisplatin (DDP) and the potential underlying anticancer...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192127/ https://www.ncbi.nlm.nih.gov/pubmed/30326933 http://dx.doi.org/10.1186/s13046-018-0922-0 |
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author | Wang, Yang Deng, Xu Yu, Chang Zhao, Guosheng Zhou, Jing Zhang, Ge Li, Ming Jiang, Dianming Quan, Zhengxue Zhang, Yuan |
author_facet | Wang, Yang Deng, Xu Yu, Chang Zhao, Guosheng Zhou, Jing Zhang, Ge Li, Ming Jiang, Dianming Quan, Zhengxue Zhang, Yuan |
author_sort | Wang, Yang |
collection | PubMed |
description | BACKGROUND: The combination of phytochemicals with chemotherapy drugs is an emerging new strategy for cancer therapy to increase antitumor responses. METHODS: 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. RESULTS: 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. CONCLUSION: 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. |
format | Online Article Text |
id | pubmed-6192127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61921272018-10-23 Synergistic inhibitory effects of capsaicin combined with cisplatin on human osteosarcoma in culture and in xenografts Wang, Yang Deng, Xu Yu, Chang Zhao, Guosheng Zhou, Jing Zhang, Ge Li, Ming Jiang, Dianming Quan, Zhengxue Zhang, Yuan J Exp Clin Cancer Res Research BACKGROUND: The combination of phytochemicals with chemotherapy drugs is an emerging new strategy for cancer therapy to increase antitumor responses. METHODS: 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. RESULTS: 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. CONCLUSION: 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. BioMed Central 2018-10-16 /pmc/articles/PMC6192127/ /pubmed/30326933 http://dx.doi.org/10.1186/s13046-018-0922-0 Text en © The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Wang, Yang Deng, Xu Yu, Chang Zhao, Guosheng Zhou, Jing Zhang, Ge Li, Ming Jiang, Dianming Quan, Zhengxue Zhang, Yuan Synergistic inhibitory effects of capsaicin combined with cisplatin on human osteosarcoma in culture and in xenografts |
title | Synergistic inhibitory effects of capsaicin combined with cisplatin on human osteosarcoma in culture and in xenografts |
title_full | Synergistic inhibitory effects of capsaicin combined with cisplatin on human osteosarcoma in culture and in xenografts |
title_fullStr | Synergistic inhibitory effects of capsaicin combined with cisplatin on human osteosarcoma in culture and in xenografts |
title_full_unstemmed | Synergistic inhibitory effects of capsaicin combined with cisplatin on human osteosarcoma in culture and in xenografts |
title_short | Synergistic inhibitory effects of capsaicin combined with cisplatin on human osteosarcoma in culture and in xenografts |
title_sort | synergistic inhibitory effects of capsaicin combined with cisplatin on human osteosarcoma in culture and in xenografts |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192127/ https://www.ncbi.nlm.nih.gov/pubmed/30326933 http://dx.doi.org/10.1186/s13046-018-0922-0 |
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