EZH2 functional dichotomy in reactive oxygen species-stratified glioblastoma.

IF 16.4 1区 医学 Q1 CLINICAL NEUROLOGY Neuro-oncology Pub Date : 2024-10-07 DOI:10.1093/neuonc/noae206
Lynnette Wei Hsien Koh, Qing You Pang, Wisna Novera, See Wee Lim, Yuk Kien Chong, Jinyue Liu, Samantha Ya Lyn Ang, Ron Weng Yee Loh, Huilin Shao, Jianhong Ching, Yulan Wang, Stephen Yip, Patrick Tan, Shang Li, David Chyi Yeu Low, Anne Phelan, Gabriel Rosser, Nguan Soon Tan, Carol Tang, Beng Ti Ang
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Abstract

Background: EZH2, well-known for its canonical methyltransferase activity in transcriptional repression in many cancers including glioblastoma (GBM), has an understudied non-canonical function critical for sustained tumor growth. Recent GBM consortial efforts reveal complex molecular heterogeneity for which therapeutic vulnerabilities correlated with subtype stratification remain relatively unexplored. Current enzymatic EZH2 inhibitors (EZH2inh) targeting its canonical SET domain show limited efficacy and lack durable response, suggesting that underlying differences in the non-canonical pathway may yield new knowledge. Here, we unveiled dual roles of the EZH2 CXC domain in therapeutically-distinct, reactive oxygen species (ROS)-stratified tumors.

Methods: We analyzed differentially expressed genes between ROS classes by examining cis-regulatory elements as well as clustering of activities and pathways to identify EZH2 as the key mediator in ROS-stratified cohorts. Pull-down assays and CRISPR knockout of EZH2 domains were used to dissect the distinct functions of EZH2 in ROS-stratified GBM cells. The efficacy of NF-κB-inducing kinase inhibitor (NIKinh) and standard-of-care temozolomide was evaluated using orthotopic patient-derived GBM xenografts.

Results: In ROS(+) tumors, CXC-mediated co-interaction with RelB drives constitutive activation of non-canonical NF-κB2 signaling, sustaining the ROS(+) chemoresistant phenotype. In contrast, in ROS(-) subtypes, PRC2 methyltransferase activity represses canonical NF-κB. Addressing the lack of EZH2inh targeting its non-methyltransferase roles, we utilized a brain-penetrant NIKinh that disrupts EZH2-RelB binding, consequently prolonging survival in orthotopic ROS(+)-implanted mice.

Conclusion: Our findings highlight the functional dichotomy of the EZH2 CXC domain in governing ROS-stratified therapeutic resistance, thereby advocating for the development of therapeutic approaches targeting its non-canonical activities and underscoring the significance of patient stratification methodologies.

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活性氧分层胶质母细胞瘤中的 EZH2 功能二分法
背景:众所周知,EZH2 在包括胶质母细胞瘤(GBM)在内的多种癌症中具有典型的转录抑制甲基转移酶活性,但它对肿瘤持续生长至关重要的非典型功能却未得到充分研究。最近的 GBM 联合研究揭示了复杂的分子异质性,而与亚型分层相关的治疗弱点仍相对缺乏研究。目前针对其规范 SET 结构域的酶法 EZH2 抑制剂(EZH2inh)显示出有限的疗效且缺乏持久的反应,这表明非规范通路的潜在差异可能会产生新的知识。在这里,我们揭示了EZH2 CXC结构域在治疗上不同的、活性氧(ROS)分层肿瘤中的双重作用:我们通过研究顺式调控元件以及活性和通路的聚类分析了ROS类别之间的差异表达基因,以确定EZH2是ROS分层队列中的关键介质。研究人员利用牵引试验和EZH2结构域的CRISPR基因敲除技术,剖析了EZH2在ROS分层的GBM细胞中的不同功能。结果显示,在ROS(+)肿瘤中,EZH2的功能与EZH2(-)和EZH2(-)(-)(-)(-)(-)(-)(-)(-)(-)结果:在ROS(+)肿瘤中,CXC介导的与RelB的共作用驱动了非经典NF-κB2信号的组成性激活,维持了ROS(+)化疗耐药表型。与此相反,在 ROS(-)亚型中,PRC2 甲基转移酶的活性抑制了典型的 NF-κB。为了解决EZH2inh缺乏针对其非甲基转移酶作用的问题,我们利用了一种能破坏EZH2-RelB结合的脑标记物NIKinh,从而延长了ROS(+)植入小鼠的存活时间:我们的研究结果凸显了 EZH2 CXC 结构域在调节 ROS 分层治疗耐药性方面的功能二分法,从而提倡开发针对其非经典活性的治疗方法,并强调了患者分层方法的重要性。
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来源期刊
Neuro-oncology
Neuro-oncology 医学-临床神经学
CiteScore
27.20
自引率
6.30%
发文量
1434
审稿时长
3-8 weeks
期刊介绍: Neuro-Oncology, the official journal of the Society for Neuro-Oncology, has been published monthly since January 2010. Affiliated with the Japan Society for Neuro-Oncology and the European Association of Neuro-Oncology, it is a global leader in the field. The journal is committed to swiftly disseminating high-quality information across all areas of neuro-oncology. It features peer-reviewed articles, reviews, symposia on various topics, abstracts from annual meetings, and updates from neuro-oncology societies worldwide.
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