Abstract
The proliferation of a human colon carcinoma cell line, COLO 201, was effectively suppressed through apoptosis in the presence of flavonoids, an ethanol extract from Vitex agnus-castus fruits. The induction of apoptosis was not inhibited by the presence of an anti-oxidant, N-acetyl-L-cysteine, whereas only HO-1 gene expression levels increased among other typical oxidative stress-associated genes examined after Vitex treatment. These results suggest that Vitex treatment activates a pathway associated with HO-1 gene activation, resulting in the induction of apoptosis in COLO 201. Results also implicate a potential clinical chemotherapeutic application of Vitex for the treatment of colon cancer patients.
MeSH terms
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Acetylcysteine / pharmacology
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Antineoplastic Agents, Phytogenic / pharmacology*
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Antioxidants / pharmacology
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Apoptosis / drug effects
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Cell Line, Tumor
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Colonic Neoplasms / drug therapy*
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DNA Fragmentation / drug effects
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Flavonoids / pharmacology*
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Free Radical Scavengers / pharmacology
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Fruit* / chemistry
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Gene Expression / drug effects
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Heme Oxygenase-1 / biosynthesis
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Heme Oxygenase-1 / drug effects
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Heme Oxygenase-1 / genetics
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Humans
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Luteolin / pharmacology
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Phytotherapy*
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Plant Extracts / pharmacology
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Reverse Transcriptase Polymerase Chain Reaction
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Vitex / chemistry
Substances
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Antineoplastic Agents, Phytogenic
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Antioxidants
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Flavonoids
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Free Radical Scavengers
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Plant Extracts
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HMOX1 protein, human
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Heme Oxygenase-1
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Luteolin
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Acetylcysteine