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| IAP Antagonists Target cIAP1 to Induce TNFx-Dependent Apoptosis |
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XIAP prevents apoptosis by binding to and inhibiting caspases, and this inhibition can be relieved bySmac Mimetics, such as Smac/DIABLO. IAP antagonist compounds (IACs) have therefore been designed to inhibit XIAP to kill tumor cells. Because XIAP inhibits postmitochondrial caspases, caspase 8 inhibitors should not block killing by IACs. Instead, we show that apoptosis caused by an IAC is blocked by the caspase 8 inhibitor crmA and thatSmac Mimetics activate NF-kB signaling via inhibtion of cIAP1. In sensitive tumor lines,
IAP antagonist induced NF-kB-stimulated production of TNFa that killed cells in an autocrine fashion. Inhibition of NF-kB reduced TNFa production, and blocking NF-kB activation or TNFa allowed tumor cells to survive IAC-induced apoptosis. Cells treated with an IAC, or those in which cIAP1 was deleted, became sensitive to apoptosis induced by exogenous TNFa, suggesting novel uses of these compounds in treating cancer. |
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