Skip to main content
. 2019 Dec 4;10(12):917. doi: 10.1038/s41419-019-2156-2

Table 1.

Characteristic of AML primary cells and cell lines.

Primary AML FAB WHO classification Age Blasts ABT-199 A1331852 S63845
[Y] [%] EC50 [µM] EC50 [µM] EC50 [µM]
30* M5 75 75 >10 >10 0.06
31* AML without maturation 83 87 0.38 >10 0.1
32* 47 34 0.04 >10 0.22
34 AML with NPM1 mutation 58 91 >10 N.D. N.D.
35 sec. AML after MDS/MPN, Overlap/AML with MDS-related changes 59 39 >10 >10 >10
38* M1 AML without maturation 71 83 0.05 >10 1
42* M4 AML with NPM1 mutation 57 25 >10 >10 0.76
43* M4 AML with NPM1 mutation 73 81 >10 >10 0.14
45 AML, NOS 33 74 >10 >10 0.1
47* M1 AML, NOS 74 71 >10 >10 >10
48 M4 AML with MDS-related changes 58 40 >10 >10 >10
55 secondary AML after MDS 79 25 2.2 9 1.1
56 M4 secondary AML after MDS 75 25 0.05 4 2.5
59* M1 AML with recurrent genetic modifications 76 71 >10 >10 0.21
60 M5 AML, NOS 22 95 0.07 >10 0.007
Cell lines
MOLM-13 M5a 0.083 >10 0.05
ML-2 M4 0.11 6.8 0.31
HL-60 M2 3 >10 1.98
KG-1 4 >10 0.49
MV4-11 M5 0.013 3.3 0.02
KASUMI-1 M2 0.77 1.8 0.15
NB4 M3 3 >10 0.06
PLB985 M2 3 >10 0.22
THP-1 M5 3 >10 0.1
MONO-MAC-6 M5 4 5.6 0.072
OCI-AML3 M4 >10 >10 1.5

EC50 values to BH3-mimetics were calculated from combined Annexin-V/FITC and anti-CD45/APC staining and flow cytometry (for primary cells) and CellTiter-Glo viability assay (for cell lines) by non-linear regression analysis using GraphPad prism. For primary AML samples, data were derived from either freshly isolated AML blasts or from previously frozen samples (*). FAB French-American-British classification system, NOS Not Otherwise Specified, MDS Myelodysplastic syndrome, ND Not determined