Figure 4
Figure 4. KR inhibits AML engraftment in NOD/SCID model. (A) Experimental design of ex vivo treatment. AML or Lin− CB cells were treated overnight with DMSO vehicle (black), 10μM KR (white), or 5μM PTL (gray), and injected into irradiated NOD/SCID mice. Eight weeks later, the surviving mice were killed and human leukemia or normal hematopoietic cell engraftment (CD45+) was measured in the injected right femur. (B) Leukemic engraftment by 2 of 4 AML samples was inhibited by KR treatment. (C) Normal hematopoietic engraftment from 5 Lin− CB pools was inhibited by KR and PTL treatment (*P < .05 and **P < .01).

KR inhibits AML engraftment in NOD/SCID model. (A) Experimental design of ex vivo treatment. AML or Lin CB cells were treated overnight with DMSO vehicle (black), 10μM KR (white), or 5μM PTL (gray), and injected into irradiated NOD/SCID mice. Eight weeks later, the surviving mice were killed and human leukemia or normal hematopoietic cell engraftment (CD45+) was measured in the injected right femur. (B) Leukemic engraftment by 2 of 4 AML samples was inhibited by KR treatment. (C) Normal hematopoietic engraftment from 5 Lin CB pools was inhibited by KR and PTL treatment (*P < .05 and **P < .01).

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