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• W2301897099 startingPage "918" @default.
• W2301897099 abstract "Organic Te(IV) compounds (organotelluranes) differing in their labile ligands exhibited anti-integrin activities in vitro and anti-metastatic properties in vivo. They underwent ligand substitution with l-cysteine, as a thiol model compound. Unlike inorganic Te(IV) compounds, the organotelluranes did not form a stable complex with cysteine, but rather immediately oxidized it. The organotelluranes inhibited integrin functions, such as adhesion, migration, and metalloproteinase secretion mediation in B16F10 murine melanoma cells. In comparison, a reduced derivative with no labile ligand inhibited adhesion of B16F10 cells to a significantly lower extent, thus pointing to the importance of the labile ligands of the Te(IV) atom. One of the organotelluranes inhibited circulating cancer cells in vivo, possibly by integrin inhibition. Our results extend the current knowledge on the reactivity and mechanism of organotelluranes with different labile ligands and highlight their clinical potential." @default.
• W2301897099 created "2016-06-24" @default.
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• W2301897099 date "2016-04-25" @default.
• W2301897099 modified "2023-10-14" @default.
• W2301897099 title "The Anticancer Activity of Organotelluranes: Potential Role in Integrin Inactivation" @default.
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• W2301897099 doi "https://doi.org/10.1002/cbic.201500614" @default.
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• W2301897099 hasPublicationYear "2016" @default.
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