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Modulation of the myeloid differentiation block in acute myeloid leukemia II

Subject Area Hematology, Oncology
Term from 2012 to 2021
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 226299880
 
Final Report Year 2020

Final Report Abstract

The main proposal was extended by an additional application for funding of a Syrian refugee as a scientist for integration into the German science system. In a certain type of AML, characterized by MLL fusions, we found that the oncogene MN1 plays an essential role for the ability of these cells to induce leukemia. We also developed a novel therapeutic approach using anti-MN1 siRNA, a small nucleotide sequence that blocks the production of MN1 protein. We developed a lipid nanoparticle-mediated siRNA delivery technology to target leukemogenic fusion genes in primary AML cells to be used as differentiation-inducing therapeutic agents. We proved its efficacy in human AML in vivo and aim to further develop this technology for clinical use. Using xenograft models, we have identified effective drug combinations that inform future clinical trials. In summary, the funding enabled us to further dissect the mechanisms how myeloid differentiation is blocked in AML cells.

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