| Literature DB >> 29764340 |
Dong-Hoon Won1, Lee-Han Kim2, Boonsil Jang3, In-Hyoung Yang2, Hye-Jeong Kwon1, Bohwan Jin4, Seung Hyun Oh5, Ju-Hee Kang5, Seong-Doo Hong1, Ji-Ae Shin1, Sung-Dae Cho1.
Abstract
Silymarin, a standardized extract from milk thistle fruits has been found to exhibit anti-cancer effects against various cancers. Here, we explored the anti-cancer activity of silymarin and its molecular target in human oral cancer in vitro and in vivo. Silymarin dose-dependently inhibited the proliferation of HSC-4 oral cancer cells and promoted caspase-dependent apoptosis. A human apoptosis protein array kit showed that death receptor 5 may be involved in silymarin-induced apoptosis, which was also shown through western blotting, immunocytochemistry, and reverse transcription-polymerase chain reaction. Silymarin increased cleaved caspase-8 and truncated Bid, leading to accumulation of cytochrome c. In addition, silymarin activated death receptor 5/caspase-8 to induce apoptotic cell death in two other oral cancer cell lines (YD15 and Ca9.22). Silymarin also suppressed tumor growth and volume without any hepatic or renal toxicity in vivo. Taken together, these results provide in vitro and in vivo evidence supporting the anti-cancer effect of silymarin and death receptor 5, and caspase-8 may be essential players in silymarin-mediated apoptosis in oral cancer.Entities:
Keywords: Silymarin; apoptosis; caspase-8; death receptor 5; oral cancer
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Year: 2018 PMID: 29764340 DOI: 10.1177/1010428318776170
Source DB: PubMed Journal: Tumour Biol ISSN: 1010-4283