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J Pharmacol Sci ; 104(4): 374-83, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17721042

ABSTRACT

Compounds such as S-allylmercaptocysteine, diallyl disulfide, and S-trityl-L-cysteine isolated from garlic have been known to be effective in chemoprevention. Nuclear transcription factor-kappaB (NF-kappaB) has been known to be an implicated factor in apoptotic cell death of several cancer cells. In this study, we investigated whether a sulfurcompound (named thiacremonone) isolated from garlic could modulate NF-kappaB activity and thereby induce apoptotic cell death of colon cancer cells. Treatment with different concentrations (30 - 150 microg/ml) of thiacremonone for various periods (0 - 48 h) inhibited colon cancer cell (SW620 and HCT116) growth followed by induction of apoptosis in a dose-dependent manner. We also found that thiacremonone modulated tumor necrosis factor-alpha (TNF-alpha) and tetradeanoyl phorbol acetate (TPA)-induced NF-kappaB transcriptional and DNA binding activity. Moreover, thiacremonone suppressed NF-kappaB target anti-apoptotic genes (Bcl-2, cIAP1/2, and XIAP) and inflammatory genes (iNOS and COX-2), whereas it induced apoptotic genes (Bax, cleaved caspse-3, and cleaved PARP) expression. These results suggest that a novel sulfurocompound from garlic inhibited colon cancer cell growth through induction of apoptotic cell death by modulating of NF-kappaB.


Subject(s)
Apoptosis/drug effects , Garlic/chemistry , Gene Expression Regulation/drug effects , NF-kappa B/drug effects , Thiophenes/pharmacology , Apoptosis/genetics , Blotting, Western , Cell Line, Tumor , Cell Survival/drug effects , Colonic Neoplasms/genetics , Colonic Neoplasms/metabolism , DNA, Neoplasm/drug effects , DNA, Neoplasm/metabolism , Dose-Response Relationship, Drug , Electrophoretic Mobility Shift Assay , Humans , NF-kappa B/genetics , NF-kappa B/metabolism , Tetradecanoylphorbol Acetate , Thiophenes/administration & dosage , Transcription, Genetic/drug effects , Tumor Necrosis Factor-alpha/drug effects , Tumor Necrosis Factor-alpha/metabolism
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