癌症研究
巨核细胞
体内
生物
骨髓增生性疾病
门1
祖细胞
突变
川地34
体外
DNA损伤
纤维化
基因剔除小鼠
净现值1
医学
突变体
真性红细胞增多症
下调和上调
表型
骨髓增生性肿瘤
髓样
白血病
阿霉素
血小板
拉明
细胞生长
细胞培养
信号转导
作者
Jeremy Wen,Anitria Cotton,Rashid Mehmood,Man Mohan,Trent Hall,Amber Broadhurst,Kevin Zhang,Yunusa Olufadi,Guolian Kang,Bridget Marcellino,J Mariano Anto Bruno Mascarenhas,Ronald Hoffman,Laura J. Janke,Sandeep Gurbuxani,Gerard M. McGeehan,John D. Crispino
标识
DOI:10.1016/j.ccell.2026.06.008
摘要
Menin inhibition, an approved therapy for KMT2A -rearranged and NPM1 mutant acute leukemia, is accompanied by decreased platelet counts in 15–20% of heavily pre-treated patients. While studying the mechanism underlying this effect, we discovered that menin inhibition reduced the numbers of megakaryocyte progenitors in human CD34 + cultures and in mice. Because megakaryocytes are key drivers of myeloproliferative neoplasms (MPNs), we investigated the extent to which menin inhibition ameliorates MPN phenotypes. We found that the menin inhibitor revumenib has potent anti-tumor activity, synergizes with ruxolitinib, and shows only subtle effects on healthy mice. Moreover, revumenib suppressed megakaryopoiesis of primary MPN patient specimens in vitro and in vivo . Importantly, genetic knockout of MEN1 and its target MEF2C phenocopied the action of revumenib, confirming an on-target effect of the drug. Together, we reveal menin as a dependency in proliferative megakaryocytes and support further evaluation of menin inhibition as a potential therapy for MPNs.
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