Synergistic Anti-cancer Activity of MH-30 in a Murine Melanoma Model Treated With Cisplatin and its Alleviated Effects Against Cisplatin-induced Toxicity in Mice

被引:11
作者
Park, Hae-Ran [1 ]
Jo, Sung-Kee [1 ]
Cho, Hyang-Hee [1 ]
Jung, Uhee [2 ]
机构
[1] Korea Atom Energy Res Inst KAERI, Radiat Res Div, Jeongeup, South Korea
[2] Korea Atom Energy Res Inst KAERI, Environm Safety Evaluat Res Div, Jeongeup, South Korea
来源
IN VIVO | 2020年 / 34卷 / 04期
关键词
Chemotherapy; melanoma; herbal; cisplatin; anticancer; cisplatin-induced toxicity; HERBAL PREPARATION HEMOHIM; INDUCED NEPHROTOXICITY; PACLITAXEL TAXOL; B16; MELANOMA; TUMOR-GROWTH; CANCER; ANTIOXIDANT; DECURSIN; PROTECTION; APOPTOSIS;
D O I
10.21873/invivo.11979
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background/Aim: Although cisplatin is an effective anticancer drug, its toxic effects on normal tissues limit its use. We developed a herbal formula, MH-30, with increased fat-soluble polyphenols by improving the manufacturing method of HemoHIM. In this study, we examined whether the combination of MH-30 with cisplatin exerts synergistic antitumor effect while it reduces cisplatin-induced toxicities. Materials and Methods: MH-30 was produced by adding the ethanol-insoluble fraction to its extract after decocting herbs in 30% ethanol and water. We used a melanoma-bearing mice model to investigate synergistic anticancer effects. The NK cell activity and cytokine levels were measured by Cr-51-release assay and ELISA. The AST, ALT, BUN, and creatinine levels were estimated in the serum. Results: MH-30 effectively inhibited melanoma growth in vitro. Furthermore, MH-30 had a synergistic effect in combination with cisplatin on melanoma growth inhibition in vitro and in vivo. In melanoma-bearing mice, cisplatin alone decreased the activity of NK cells and the levels of IL-2 and IFN-gamma, which were effectively restored by the combination of MH-30 with cisplatin. Combined treatment with MH-30 and cisplatin significantly inhibited the cisplatin-induced increase in the levels of AST, ALT, BUN, and creatinine. Conclusion: Combination of MH-30 with cisplatin may be a beneficial anticancer treatment with reduced adverse effects.
引用
收藏
页码:1845 / 1856
页数:12
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