癌症研究
白血病
共价键
化学
药理学
医学
免疫学
有机化学
作者
Tamara Maes,Cristina Mascaró,Iñigo Tirapu,Angels Estiarte,Filippo Ciceri,Serena Lunardi,Nathalie Guibourt,Alvaro Perdones,Michele MP Lufino,Tim C. P. Somervaille,Daniel H. Wiseman,Cihangir Duy,Ari Melnick,Christophe Willekens,Alberto Ortega,Marc Martinell,Núria Valls,Guido Kurz,Matthew C. T. Fyfe,Julio C. Castro‐Palomino,Carlos Buesa
出处
期刊:Cancer Cell
[Elsevier]
日期:2018-03-01
卷期号:33 (3): 495-511.e12
被引量:257
标识
DOI:10.1016/j.ccell.2018.02.002
摘要
The lysine-specific demethylase KDM1A is a key regulator of stem cell potential in acute myeloid leukemia (AML). ORY-1001 is a highly potent and selective KDM1A inhibitor that induces H3K4me2 accumulation on KDM1A target genes, blast differentiation, and reduction of leukemic stem cell capacity in AML. ORY-1001 exhibits potent synergy with standard-of-care drugs and selective epigenetic inhibitors, reduces growth of an AML xenograft model, and extends survival in a mouse PDX (patient-derived xenograft) model of T cell acute leukemia. Surrogate pharmacodynamic biomarkers developed based on expression changes in leukemia cell lines were translated to samples from patients treated with ORY-1001. ORY-1001 is a selective KDM1A inhibitor in clinical trials and is currently being evaluated in patients with leukemia and solid tumors.
科研通智能强力驱动
Strongly Powered by AbleSci AI