Back to Search
Start Over
In vitro and in vivo anti-cancer activity of silymarin on oral cancer
- Source :
- Tumor Biology, Vol 40 (2018)
- Publication Year :
- 2018
- Publisher :
- IOS Press, 2018.
-
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.
- Subjects :
- 0301 basic medicine
Antineoplastic Agents
Apoptosis
Pharmacology
Caspase 8
03 medical and health sciences
0302 clinical medicine
In vivo
Cell Line, Tumor
medicine
Humans
RC254-282
Cell Proliferation
Chemistry
Cytochromes c
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
Cancer
General Medicine
medicine.disease
In vitro
Blot
Receptors, TNF-Related Apoptosis-Inducing Ligand
030104 developmental biology
030220 oncology & carcinogenesis
Toxicity
Cancer cell
Mouth Neoplasms
Silymarin
Subjects
Details
- ISSN :
- 14230380 and 10104283
- Volume :
- 40
- Database :
- OpenAIRE
- Journal :
- Tumor Biology
- Accession number :
- edsair.doi.dedup.....b8792d1eeeb02cc410154a40895f7cdb
- Full Text :
- https://doi.org/10.1177/1010428318776170