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KDM6去甲基化酶整合DNA修复基因调控,而KDM6A的缺失使人类急性髓系白血病对PARP和BCL2抑制敏感。

KDM6 demethylases integrate DNA repair gene regulation and loss of KDM6A sensitizes human acute myeloid leukemia to PARP and BCL2 inhibition.

作者信息

Boila Liberalis Debraj, Ghosh Subhadeep, Bandyopadhyay Subham K, Jin Liqing, Murison Alex, Zeng Andy G X, Shaikh Wasim, Bhowmik Satyaki, Muddineni Siva Sai Naga Anurag, Biswas Mayukh, Sinha Sayantani, Chatterjee Shankha Subhra, Mbong Nathan, Gan Olga I, Bose Anwesha, Chakraborty Sayan, Arruda Andrea, Kennedy James A, Mitchell Amanda, Lechman Eric R, Banerjee Debasis, Milyavsky Michael, Minden Mark D, Dick John E, Sengupta Amitava

机构信息

Stem Cell & Leukemia Lab, CSIR-Indian Institute of Chemical Biology, IICB-Translational Research Unit of Excellence, Salt Lake, Kolkata, 700091, West Bengal, India.

Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA, 98109, USA.

出版信息

Leukemia. 2023 Apr;37(4):751-764. doi: 10.1038/s41375-023-01833-z. Epub 2023 Jan 31.

Abstract

Acute myeloid leukemia (AML) is a heterogeneous, aggressive malignancy with dismal prognosis and with limited availability of targeted therapies. Epigenetic deregulation contributes to AML pathogenesis. KDM6 proteins are histone-3-lysine-27-demethylases that play context-dependent roles in AML. We inform that KDM6-demethylase function critically regulates DNA-damage-repair-(DDR) gene expression in AML. Mechanistically, KDM6 expression is regulated by genotoxic stress, with deficiency of KDM6A-(UTX) and KDM6B-(JMJD3) impairing DDR transcriptional activation and compromising repair potential. Acquired KDM6A loss-of-function mutations are implicated in chemoresistance, although a significant percentage of relapsed-AML has upregulated KDM6A. Olaparib treatment reduced engraftment of KDM6A-mutant-AML-patient-derived xenografts, highlighting synthetic lethality using Poly-(ADP-ribose)-polymerase-(PARP)-inhibition. Crucially, a higher KDM6A expression is correlated with venetoclax tolerance. Loss of KDM6A increased mitochondrial activity, BCL2 expression, and sensitized AML cells to venetoclax. Additionally, BCL2A1 associates with venetoclax resistance, and KDM6A loss was accompanied with a downregulated BCL2A1. Corroborating these results, dual targeting of PARP and BCL2 was superior to PARP or BCL2 inhibitor monotherapy in inducing AML apoptosis, and primary AML cells carrying KDM6A-domain mutations were even more sensitive to the combination. Together, our study illustrates a mechanistic rationale in support of a novel combination therapy for AML based on subtype-heterogeneity, and establishes KDM6A as a molecular regulator for determining therapeutic efficacy.

摘要

急性髓系白血病(AML)是一种异质性、侵袭性恶性肿瘤,预后不佳,靶向治疗的可用性有限。表观遗传失调促成了AML的发病机制。KDM6蛋白是组蛋白3赖氨酸27去甲基化酶,在AML中发挥着依赖于背景的作用。我们发现KDM6去甲基化酶功能在AML中关键调节DNA损伤修复(DDR)基因表达。从机制上讲,KDM6表达受基因毒性应激调节,KDM6A(UTX)和KDM6B(JMJD3)的缺失会损害DDR转录激活并损害修复潜力。获得性KDM6A功能丧失突变与化疗耐药有关,尽管相当一部分复发AML的KDM6A上调。奥拉帕利治疗减少了KDM6A突变的AML患者来源异种移植物的植入,突出了使用聚(ADP核糖)聚合酶(PARP)抑制的合成致死性。至关重要的是,较高的KDM6A表达与维奈托克耐受性相关。KDM6A的缺失增加了线粒体活性、BCL2表达,并使AML细胞对维奈托克敏感。此外,BCL2A1与维奈托克耐药相关,KDM6A的缺失伴随着BCL2A1的下调。证实这些结果的是,PARP和BCL2的双重靶向在诱导AML细胞凋亡方面优于PARP或BCL2抑制剂单药治疗,携带KDM6A结构域突变的原发性AML细胞对联合治疗甚至更敏感。总之,我们的研究阐明了一种基于亚型异质性支持AML新型联合治疗的机制原理,并将KDM6A确立为决定治疗效果的分子调节剂。

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