癌症研究
Hox基因
净现值1
髓样
髓性白血病
下调和上调
医学
基因
生物
转录因子
遗传学
核型
染色体
作者
Michael W.M. Kühn,Arnold Ganser
摘要
The treatment of acute myeloid leukaemia (AML) has changed fundamentally in the last decade with many new targeted therapies entering clinics. Some of the most interesting agents under development are Menin inhibitors which interfere with the interaction of Menin with wild‐type (wt) KMT2A or a KMT2A‐fusion protein and thereby downregulate the leukaemic gene expression (MEIS1, PBX3, HOX) in NPM1 mutant or KMT2A ‐rearranged leukaemia. Other HOX and MEIS1 expressing leukaemias may also be sensitive to Menin inhibition. Following the encouraging results as monotherapy in refractory and relapsed AML, the combination of Menin inhibitors with chemotherapeutic agents and other targeted drugs is being investigated clinically.
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