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 α 4β 1 integrin, in the murine melanoma B16F10 cells. Ajoene induced a significant reduction in B16F10 viability (IC 50=62 μM), 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 μM altered the α 4β 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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