Epigenetic vulnerabilities of leukemia harboring inactivating EZH2 mutations

被引:4
作者
Alqazzaz, Mona A. [1 ,2 ]
Luciani, Genna M. [2 ]
Vu, Victoria [1 ,2 ]
Machado, Raquel A. C. [1 ]
Szewczyk, Magdalena M. [1 ]
Adamson, Ella C. [1 ,3 ]
Cheon, Sehyun [1 ,3 ]
Li, Fengling [1 ]
Arrowsmith, Cheryl H. [1 ,2 ]
Minden, Mark D. [2 ]
Barsyte-Lovejoy, Dalia [1 ,3 ,4 ]
机构
[1] Univ Toronto, Struct Genom Consortium, Toronto, ON, Canada
[2] Univ Toronto, Princess Margaret Canc Ctr, Dept Med Biophys, Toronto, ON, Canada
[3] Univ Toronto, Dept Pharmacol & Toxicol, Toronto, ON, Canada
[4] Univ Toronto, Struct Genom Consortium, 101 Coll St,MaRS South Tw 700, Toronto, ON M5G 1L7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
METHYLTRANSFERASE GENE EZH2; SOMATIC MUTATIONS; EXPRESSION; INHIBITOR; LANDSCAPE; PROGNOSIS; CELLS; PRC2; EED;
D O I
10.1016/j.exphem.2023.11.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Epigenetic regulators, such as the polycomb repressive complex 2 (PRC2), play a critical role in both normal development and carcinogenesis. Mutations and functional dysregulation of PRC2 complex components, such as EZH2, are implicated in various forms of cancer and associated with poor prognosis. This study investigated the epigenetic vulnerabilities of acute myeloid leukemia (AML) and myelodysplastic/myeloproliferative disorders (MDS/MPN) by performing a chemical probe screen in patient cells. Paradoxically, we observed increased sensitivity to EZH2 and embryonic ectoderm development (EED) inhibitors in AML and MDS/MPN patient cells harboring EZH2 mutations. Expression analysis indicated that EZH2 inhibition elicited upregulation of pathways responsible for cell death and growth arrest, specifically in patient cells with mutant EZH2. The identified EZH2 mutations had drastically reduced catalytic activity, resulting in lower cellular H3K27me3 levels, and were associated with decreased EZH2 and PRC2 component EED protein levels. Overall, this study provides an important understanding of the role of EZH2 dysregulation in blood cancers and may indicate disease etiology for these poor prognosis AML and MDS/MPN cases. (c) 2023 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 13
页数:13
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