TY - JOUR
T1 - Thermal ablation versus conventional regional hyperthermia has greater anti-tumor activity against melanoma in mice by upregulating CD4+ cells and enhancing IL-2 secretion
AU - Zhang, Yingying
AU - Zhang, Wei
AU - Geng, Cuanying
AU - Lin, Tongjun
AU - Wang, Xiaowen
AU - Zhao, Lingyun
AU - Tang, Jintian
N1 - Funding Information:
This work was supported by the National Natural Science Foundation of China (Grant Nos. 30571779 and 10775085 ).
PY - 2009/12
Y1 - 2009/12
N2 - To determine whether conventional hyperthermia (42-45°C) or ablation therapy (> 50°C) achieves better synergistic effects on direct cytotoxicity and anti-tumor immunity, we compared the therapeutic effects of two hyperthermia temperatures, 43 and 55°C, in terms of cytotoxicity and upregulation of immune functions in a mouse malignant melanoma model. Melanoma-bearing mice were treated by directly applying regional hyperthermia to the tumor nodule with a heating light at a temperature of 43°C for 30 min or 55°C for 10 min. The tumor growth curve and mice survival rate were observed. To investigate the hyperthermia-induced immunological response, peripheral blood CD4+ and CD8+ T cells and the serum IL-2 level were determined. Our results indicated that application of regional hyperthermia at the ablation temperature (such as 55°C) achieved better synergistic anti-tumor effects than did conventional hyperthermia (43°C). Significant increases in the number of peripheral blood CD4+ T cells and the serum IL-2 level likely contributed to the underlying mechanism.
AB - To determine whether conventional hyperthermia (42-45°C) or ablation therapy (> 50°C) achieves better synergistic effects on direct cytotoxicity and anti-tumor immunity, we compared the therapeutic effects of two hyperthermia temperatures, 43 and 55°C, in terms of cytotoxicity and upregulation of immune functions in a mouse malignant melanoma model. Melanoma-bearing mice were treated by directly applying regional hyperthermia to the tumor nodule with a heating light at a temperature of 43°C for 30 min or 55°C for 10 min. The tumor growth curve and mice survival rate were observed. To investigate the hyperthermia-induced immunological response, peripheral blood CD4+ and CD8+ T cells and the serum IL-2 level were determined. Our results indicated that application of regional hyperthermia at the ablation temperature (such as 55°C) achieved better synergistic anti-tumor effects than did conventional hyperthermia (43°C). Significant increases in the number of peripheral blood CD4+ T cells and the serum IL-2 level likely contributed to the underlying mechanism.
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U2 - 10.1016/j.pnsc.2009.05.007
DO - 10.1016/j.pnsc.2009.05.007
M3 - Article
AN - SCOPUS:72749123732
SN - 1002-0071
VL - 19
SP - 1699
EP - 1704
JO - Progress in Natural Science: Materials International
JF - Progress in Natural Science: Materials International
IS - 12
ER -