標題: | Potential enhancement of host immunity and anti-tumor efficacy of nanoscale curcumin and resveratrol in colorectal cancers by modulated electro- hyperthermia |
作者: | Kuo, I-Ming Lee, Jih-Jong Wang, Yu-Shan Chiang, Hsin-Chien Huang, Cheng-Chung Hsieh, Pei-Jong Han, Winston Ke, Chiao-Hsu Liao, Albert T. C. Lin, Chen-Si 分子醫學與生物工程研究所 Institute of Molecular Medicine and Bioengineering |
關鍵字: | Modulated electro-hyperthermia (mEHT);Curcumin;Resveratrol;Nanosized;Apoptosis;Tumor microenvironment |
公開日期: | 29-六月-2020 |
摘要: | BackgroundModulated electro-hyperthermia (mEHT) is a form of hyperthermia used in cancer treatment. mEHT has demonstrated the ability to activate host immunity by inducing the release of heat shock proteins, triggering apoptosis, and destroying the integrity of cell membranes to enhance cellular uptake of chemo-drugs in tumor cells. Both curcumin and resveratrol are phytochemicals that function as effective antioxidants, immune activators, and potential inhibitors of tumor development. However, poor bioavailability is a major obstacle for use in clinical cancer treatment.MethodsThis purpose of this study was to investigate whether mEHT can increase anti-cancer efficacy of nanosized curcumin and resveratrol in in vitro and in vivo models. The in vitro study included cell proliferation assay, cell cycle, and apoptosis analysis. Serum concentration was analyzed for the absorption of curcumin and resveratrol in SD rat model. The in vivo CT26/BALB/c animal tumor model was used for validating the safety, tumor growth curve, and immune cell infiltration within tumor tissues after combined mEHT/curcumin/resveratrol treatment.ResultsThe results indicate co-treatment of mEHT with nano-curcumin and resveratrol significantly induced cell cycle arrest and apoptosis of CT26 cells. The serum concentrations of curcumin and resveratrol were significantly elevated when mEHT was applied. The combination also inhibited the growth of CT26 colon cancer by inducing apoptosis and HSP70 expression of tumor cells while recruiting CD3+ T-cells and F4/80+ macrophages.ConclusionsThe results of this study have suggested that this natural, non-toxic compound can be an effective anti-tumor strategy for clinical cancer therapy. mEHT can enable cellular uptake of potential anti-tumor materials and create a favorable tumor microenvironment for an immunological chain reaction that improves the success of combined treatments of curcumin and resveratrol. |
URI: | http://dx.doi.org/10.1186/s12885-020-07072-0 http://hdl.handle.net/11536/154841 |
DOI: | 10.1186/s12885-020-07072-0 |
期刊: | BMC CANCER |
Volume: | 20 |
Issue: | 1 |
起始頁: | 0 |
結束頁: | 0 |
顯示於類別: | 期刊論文 |