Author/Authors :
Jin، نويسنده , , Linhua and Tabe، نويسنده , , Yoko and Kojima، نويسنده , , Kensuke and Zhou، نويسنده , , Yixin and Pittaluga، نويسنده , , Stefania and Konopleva، نويسنده , , Marina and Miida، نويسنده , , Takashi and Raffeld، نويسنده , , Mark، نويسنده ,
Abstract :
This study demonstrated a pronounced synergistic growth-inhibitory effect of an MDM2 inhibitor Nutlin-3 and a proteasome inhibitor bortezomib in mantle cell lymphoma (MCL) cells regardless of TP53 mutant status and innate bortezomib sensitivity. In the mutant TP53 MCL cells which are intrinsically resistant to bortezomib, the combination of Nutlin-3/bortezomib synergistically induced cytotoxicity through the mitochondrial apoptotic pathway mediated by transcription-independent upregulation of NOXA, sequestration of MCL-1, activation of BAX, BAK, caspase-9 and -3. In the bortezomib sensitive wild-type TP53 MCL cells, the Nutlin-3/bortezomib combination caused G0/G1 cell cycle arrest followed by the increase in apoptosis induction. These findings indicate potential therapeutic efficacy of Nutlin-3/bortezomib combination for the treatment of chemorefractory MCL.
Keywords :
Nutlin-3 , TP53 , Mantle cell lymphoma , bortezomib , MDM2