癌症研究
生物
表观遗传学
髓系白血病
抑制器
白血病
髓样
基因
抑制因子
抑癌基因
癌症
功能(生物学)
癸他滨
基因沉默
髓源性抑制细胞
突变
组蛋白
损失函数
柔红霉素
小RNA
流式细胞术
HDAC4型
癌细胞
表观遗传疗法
免疫学
基因表达调控
自噬
心理压抑
作者
Alexander Arnuk,Cuijuan Han,Abimbola Eunice. Lawal,Bofei Wang,Sadik Karma,Zhiping Zhang,Mhd Yousuf Yassouf,Sakthi H. Rajendran,Harshpreet Chandok,Madeline L. Eller,Sogand Sajedi,Meryl McKenna,Eve Herman,Louisa Hagen,Bettina Nadorp,Zengshuo Mo,Hector Orellana,A. Tsirigos,Pedro Miura,Hussein A. Abbas
标识
DOI:10.1126/scitranslmed.ady2936
摘要
Inactivation of tumor suppressor genes (TSGs) imparts a cellular fitness in cancers, including in acute myeloid leukemia (AML). The detection of silenced TSGs without direct mutations presents challenges in designing targeted cancer treatments, yet it also opens a therapeutic opportunity to restore their function. In this study, we identified the transcriptional repressor ZBTB7A as a TSG that is down-regulated in samples from patients with AML and is associated with poor survival outcomes. Loss of ZBTB7A amplifies TNF signaling, driving a dysfunctional inflammatory state that accelerates AML progression in vivo. Mechanistically, the mRNA decay factor ZFP36L2 binds to the 3′ untranslated region (3′UTR) of ZBTB7A , promoting its transcript degradation in human AML cells. To identify therapeutic targets, we developed a CRISPR-based screening approach coupled with fluorescence in situ hybridization and flow cytometry (FISH-Flow), pinpointing the KDM4 family of histone demethylases as a vulnerability to restore ZBTB7A function. Pharmacologic inhibition of KDM4 up-regulated ZBTB7A expression, promoted terminal differentiation in patient-derived xenograft models, and demonstrated broad antileukemic efficacy across AML subtypes as well as preserved normal hematopoiesis. These findings reveal regulatory mechanisms of ZBTB7A and support epigenetic therapy as a promising strategy to reactivate its tumor suppressor function in hematologic cancers.
科研通智能强力驱动
Strongly Powered by AbleSci AI