Antiproliferative Activity and Induction of Apoptosis in Human Melanoma Cells by Houttuynia cordata Thunb Extract

被引:35
|
作者
Yanarojana, Mongkol [1 ]
Nararatwanchai, Thamthiwat [1 ]
Thairat, Sarut [2 ]
Tancharoen, Salunya [2 ]
机构
[1] Mae Fah Luang Univ, Sch Antiaging & Regenerat Med, Bangkok, Thailand
[2] Mahidol Univ, Dept Pharmacol, Fac Dent, 6 Yothe Rd, Bangkok 10400, Thailand
关键词
Houttuynia cordata Thunb; melanoma; apoptosis; caspase; mitogen-activated protein kinase; high mobility group box 1; UP-REGULATION; CANCER; CASPASES; ANTHOCYANINS; SUPPRESSION; STATISTICS; ACTIVATION; GROWTH; HMGB1;
D O I
10.21873/anticanres.12119
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: To analyze the apoptotic effect of Houttuynia cordata Thunb (HCT) extract on human melanoma A375 cells and its underlying mechanisms. Materials and Methods: The effects of HCT on cell death were determined using the MTT assay. Hoechst 33342 staining was conducted to confirm the detection of cell apoptosis. Caspase-3 and caspase-8 mRNA and cleaved protein levels were investigated by RT-PCR and western blotting, respectively. The release of high mobility group box 1 (HMGB1) and phosphorylation of mitogen-activated protein kinase (MAPK) were determined by ELISA. Results: Caspase-3 and caspase-8 specific inhibitors suppressed HCT-induced cell death. HCT increased caspase-3 and caspase-8 mRNA, protein levels, and caspase activities in a concentration-and time-dependent manner. HCT induced MAPK phosphorylation in a time-dependent fashion. Pretreatment of cells with a selective inhibitor of p38 MAPK reduced apoptosis and reversed the levels of HMGB1 release in response to HCT treatment. Conclusion: HCT induces A375 programmed cell death by activating the caspase-dependent pathway and by p38 phosphorylation associated with HMGB1 reduction.
引用
收藏
页码:6619 / 6628
页数:10
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