Author/Authors :
Petersen، نويسنده , , Sean L. and Wang، نويسنده , , Lai and Yalcin-Chin، نويسنده , , Asligul and Li، نويسنده , , Lin and Peyton، نويسنده , , Michael and Minna، نويسنده , , John and Harran، نويسنده , , Patrick and Wang، نويسنده , , Xiaodong، نويسنده ,
Abstract :
Summary
l-molecule mimetic of Smac/Diablo that specifically counters the apoptosis-inhibiting activity of IAP proteins has been shown to enhance apoptosis induced by cell surface death receptors as well as chemotherapeutic drugs. Survey of a panel of 50 human non-small-cell lung cancer cell lines has revealed, surprisingly, that roughly one-quarter of these lines are sensitive to the treatment of Smac mimetic alone, suggesting that an apoptotic signal has been turned on in these cells and is held in check by IAP proteins. This signal has now been identified as the autocrine-secreted cytokine tumor necrosis factor alpha (TNFα). In response to autocrine TNFα signaling, the Smac mimetic promotes formation of a RIPK1-dependent caspase-8-activating complex, leading to apoptosis.