Abstract |
In this study we evaluated the hypothesis that the antitumor activity of ajoene could be associated with its apoptosis-inducing effect, and with its ability to block the expression of the alpha(4)beta(1) integrin, in the murine melanoma B16F10 cells. Ajoene induced a significant reduction in B16F10 viability (IC(50)=62 microM), in a dose-dependent manner. Flow cytometric analysis showed that the cytotoxic effect of this compound was associated with caspase-3 activation. Ajoene at 25 microM altered the alpha(4)beta(1) integrin expression on B16F10, and induced a significant reduction in the adhesion of these cells to an endothelial cell monolayer.
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Authors | Eliades Ledezma, Rafael Apitz-Castro, José Cardier |
Journal | Cancer letters
(Cancer Lett)
Vol. 206
Issue 1
Pg. 35-41
(Mar 31 2004)
ISSN: 0304-3835 [Print] Ireland |
PMID | 15019157
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antineoplastic Agents
- Disulfides
- Integrin alpha4beta1
- Plant Extracts
- Sulfoxides
- ajoene
- Glutathione Reductase
- Casp3 protein, mouse
- Caspase 3
- Caspases
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Topics |
- Animals
- Antineoplastic Agents
(pharmacology)
- Apoptosis
(drug effects)
- Caspase 3
- Caspases
(metabolism)
- Cell Adhesion
(drug effects)
- Colony-Forming Units Assay
- Disulfides
(pharmacology)
- Flow Cytometry
- Garlic
(chemistry)
- Glutathione Reductase
(antagonists & inhibitors)
- Integrin alpha4beta1
(metabolism)
- Melanoma, Experimental
(metabolism, pathology)
- Mice
- Plant Extracts
(pharmacology)
- Sulfoxides
- Tumor Cells, Cultured
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