Apoptotic Effects of 6-Gingerol in LNCaP Human Prostate Cancer Cells
Objective: 6-Gingerol, one component of ginger (Zingiber officinale) compound, has been known to possess anti-inflammatory, analgesic,anti-emetic, and anti-cancer effects. In this study, the apoptotic ability of 6-gingerol was investigated in human prostate cancer cells. Methods: 3-(4,5-Dimethylthia...
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Veröffentlicht in: | Soonchunhyang medical science 2011, 17(2), , pp.75-79 |
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Zusammenfassung: | Objective: 6-Gingerol, one component of ginger (Zingiber officinale) compound, has been known to possess anti-inflammatory, analgesic,anti-emetic, and anti-cancer effects. In this study, the apoptotic ability of 6-gingerol was investigated in human prostate cancer cells.
Methods: 3-(4,5-Dimethylthiazol-2-yl)- 2,5-diphenyl-tetrazolium bromide (MTT) assay, flow cytometry, and western blot analysis were done in LNCaP human prostate cancer cell lines treated with the various doses of 6-gingerol for the different durations of drug exposure.
Results: 6-Gingerol in doses ranging from 100 to 300 μM induced dose- and time-dependent inhibition of cell viability in prostate cancer cells by using MTT assay. Maximal inhibition of cell viability was observed at 300 μM of 6-gingerol for 48 hours treatment in LNCaP cells. 6-Gingerol at the dose of 100 μM did not produce any significant change in apoptotic cells in flow cytometry analysis.
However, significant increase in sub-G0/G1 phase was observed in cells treated with 200 and 300 μM of 6-gingerol. Any significant cell cycle arrest was not induced by 6-gingerol. In western blotting analysis, expression of caspase-3 was not evident in cells treated with 6-gingerol for 24 hours. However, 48 hours treatment with 6-gingerol altered the expression of caspase-3 in LNCaP cells. Expression of cleaved poly showed the dose-dependent fashion in both 24 hours and 48 hours treatment of 6-gingerol.
Conclusion: These observations suggest that 6-gingerol may induce apoptosis in LNCaP human prostate cancer cells. KCI Citation Count: 0 |
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ISSN: | 2233-4289 2233-4297 |
DOI: | 10.15746/sms.11.017 |