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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.
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页码:6619 / 6628
页数:10
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