Table 2

In vitro sensitization of MK1775 to Ara-C in AML, ALL, and CML cells

Cell line72 h
96 h
AraC → MK1775AraC + MK1775AraC → MK1775AraC + MK1775
TF-1 1.6 2.3 2.3 3.6 
THP-1 12.0 12.0 32.0 97.0 
HEL 1.3 1.8 3.1 3.9 
MDS-L 4.0 5.0 1.3 4.0* 
MV4;11 12.0 12.0 7.6 11.5* 
GM03761 4.0 4.5 2.9 27.0* 
K562 1.4 2.9 3.4 17.0 
Jurkat 10.0 15.0 2.8 7.4 
Cell line72 h
96 h
AraC → MK1775AraC + MK1775AraC → MK1775AraC + MK1775
TF-1 1.6 2.3 2.3 3.6 
THP-1 12.0 12.0 32.0 97.0 
HEL 1.3 1.8 3.1 3.9 
MDS-L 4.0 5.0 1.3 4.0* 
MV4;11 12.0 12.0 7.6 11.5* 
GM03761 4.0 4.5 2.9 27.0* 
K562 1.4 2.9 3.4 17.0 
Jurkat 10.0 15.0 2.8 7.4 

Summary of Ara-C EC50 shifts of 8 AML, ALL, and CML cell lines treated with Ara-C alone or in combination with MK1775 at 50, 100, and 300nM. The -fold sensitization is shown for Ara-C followed by MK1775 (AraC → MK; sequential dosing) and AraC + MK1775 (AraC + MK; simultaneous dosing) at 72 and 96 hours. Table shows the -fold shifts for 300nM MK1775 except as indicated. See supplemental Figure 5B for corresponding drug-dose–response curves/graphs from simultaneous dosing.

*

50nM MK1775.

100nM MK1775.

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