Table 2

Cotreatment of DLBCL cells with CFZ and vorinostat induces pronounced cell cycle arrest in G2M

Cell cycle (phase)ControlCFZVorinostatCFZ plus vorinostat
SUDHL4     
    G0G1 45.9 ± 3.8 31.9 ± 0.9 65.8 ± 1.6 5.9 ± 3.4 
    G215.1 ± 1.6 28.2 ± 1.4* 15.4 ± 1.2 78.7 ± 4.9 
    S 35.4 ± 2.8 40.4 ± 1.6 16.7 ± 1.3 15.6 ± 1.7 
OCI-LY10     
    G0G1 30.7 ± 1.7 23.4 ± 1.6 25.4 ± 3.1 5.9 ± 1.5 
    G212.5 ± 1.5 21.8 ± 2.2* 15.1 ± 1.7 50.2 ± 1.7 
    S 53.5 ± 4.5 54.7 ± 0.7 56.4 ± 3.1 44.4 ± 1.1 
Cell cycle (phase)ControlCFZVorinostatCFZ plus vorinostat
SUDHL4     
    G0G1 45.9 ± 3.8 31.9 ± 0.9 65.8 ± 1.6 5.9 ± 3.4 
    G215.1 ± 1.6 28.2 ± 1.4* 15.4 ± 1.2 78.7 ± 4.9 
    S 35.4 ± 2.8 40.4 ± 1.6 16.7 ± 1.3 15.6 ± 1.7 
OCI-LY10     
    G0G1 30.7 ± 1.7 23.4 ± 1.6 25.4 ± 3.1 5.9 ± 1.5 
    G212.5 ± 1.5 21.8 ± 2.2* 15.1 ± 1.7 50.2 ± 1.7 
    S 53.5 ± 4.5 54.7 ± 0.7 56.4 ± 3.1 44.4 ± 1.1 

SUDHL4 cells were treated with 4.0nM CFZ with or without 1.5μM vorinostat, or OCI- LY10 cells were treated with 7.0nM CFZ with or without 1.5μM vorinostat for 18 hours. After treatment, cells were collected, fixed in ice-cold methanol at a ratio of 1 mL phosphate-buffered saline to 3 mL methanol, and cell-cycle traverse was analyzed by flow cytometry using Modfit software as described in “Cell-cycle analysis.”

DLBCL indicates ; and CFZ, carfilzomib.

*

Significantly greater than values for untreated control cells (P < .02).

Significantly greater than values for cells treated with CFZ alone (P < .005).

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