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Cell Cycle News & Views

Inhibition of IκB kinase in Notch signaling activates FOXO3a

Page 2417 | Published online: 01 Jul 2012

Figures & data

Figure 1. Schematic model depicting the role of IKK inhibition in regulating FOXO3a and NFκB nuclear translocation. In T-ALL, when Notch is mutated and constitutive active, IKK is constant active, which phosphorylates IκB and elicits NFκB nuclear translocation and promote tumorigenesis. The active IKK also sequesters FOXO3a in the cytoplasm. Inhibition of IKK by BMS-345541 triggers FOXO3a nuclear translocation and induces cell cycle arrest and apoptosis.

Figure 1. Schematic model depicting the role of IKK inhibition in regulating FOXO3a and NFκB nuclear translocation. In T-ALL, when Notch is mutated and constitutive active, IKK is constant active, which phosphorylates IκB and elicits NFκB nuclear translocation and promote tumorigenesis. The active IKK also sequesters FOXO3a in the cytoplasm. Inhibition of IKK by BMS-345541 triggers FOXO3a nuclear translocation and induces cell cycle arrest and apoptosis.