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. 2013 Nov 11;8(11):e78897. doi: 10.1371/journal.pone.0078897

Table 2. Presence of FLT3-ITD and mutated NPM1 in ALDHbright and ALDHlow compartments in CD34-positive AML.

Patient # FLT3-ITD CD34– cells CD34+CD38 ALDHlow CD34+CD38– ALDHbright
575 pos 50% ITD wt
808 pos 50% ITD wt
951 pos 42% ITD wt
966 pos 43% ITD wt
1263 pos 60% ITD wt
Patient # NPM1 CD34cells CD34+CD38 ALDHlow CD34+CD38 ALDHbright
575 mut mut wt
808 mut mut wt
945 mut mut wt (<5%)
670 mut mut wt

Detection of molecular aberrancies in CD34+CD38– ALDHbright and ALDHlow compartments of CD34-positive AML. The FLT3-ITD percentage is determined in the total leukemic blast population (data not shown), the CD34– cell population and the CD34+CD38-ALDHlow and CD34+CD38-ALDHbright compartments. The NPM1 mutation analysis is not quantative. # the ALDHbright compartment contained in one case a small mutant peak (AML-945), likely caused by relatively poor separation of ALDHbright and ALDHlow populations due to overlap in the boundary region.