AS602868, a pharmacological inhibitor of IKK2, reveals the apoptotic potential of TNF-α in Jurkat leukemic cells

NF- κ B transcription factors promote survival in numerous cell types via induction of antiapoptotic genes. Pharmacological blockade of the IKK2 kinase with AS602868, a specific inhibitor that competes with ATP binding, prevented TNF- α -induced NF- κ B activation in Jurkat leukemic T cells. While T...

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Veröffentlicht in:Oncogene 2003-11, Vol.22 (50), p.8187-8194
Hauptverfasser: Frelin, Catherine, Imbert, Véronique, Griessinger, Emmanuel, Loubat, Agnès, Dreano, Michel, Peyron, Jean-François
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Sprache:eng
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Zusammenfassung:NF- κ B transcription factors promote survival in numerous cell types via induction of antiapoptotic genes. Pharmacological blockade of the IKK2 kinase with AS602868, a specific inhibitor that competes with ATP binding, prevented TNF- α -induced NF- κ B activation in Jurkat leukemic T cells. While TNF- α by itself had no effect on Jurkat survival, the addition of AS602868 induced cell death, visualized by DNA fragmentation and sub-G1 analysis. A disruption of the mitochondrial potential followed by activation of caspases 9 and 3 was observed in cells treated by the combination TNF- α +AS602868. Quantitative real-time PCR demonstrated that AS602868 prevented TNF- α induction of the antiapoptotic genes coding for c-IAP-2, Bclx, Bfl-1/A1 and Traf-1. The use of a specific IKK2 inhibitor appears, therefore, as an interesting pharmaceutical strategy to increase the cell's sensitivity towards apoptotic effectors.
ISSN:0950-9232
1476-5594
DOI:10.1038/sj.onc.1206963