This is consistent with the highly significant reduction induced in BM leukemic burden after nanotoxin treatment in vivo, using the same mechanism of action as ITs that kill non-dividing cells by inhibiting eEF-2 and protein translation synthesis [ 57 ].
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T22-PE24-H6 Nanotoxin Selectively Kills CXCR4-High Expressing AML Patient Cells In Vitro and Potently Blocks Dissemination In Vivo.
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