| Literature DB >> 15019157 |
Eliades Ledezma1, Rafael Apitz-Castro, José Cardier.
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.Entities:
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Year: 2004 PMID: 15019157 DOI: 10.1016/j.canlet.2003.10.031
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679