Evidence map›Paper›PMID 39373211›Full record

ArticleNeuro-oncology2025

EZH2 functional dichotomy in reactive oxygen species-stratified glioblastoma.

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 and 10 more

Abstract read
In one paragraph

Article in Neuro-oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Cancer stem cells synthesize proline to attenuate oxidative stress.The Journal of clinical investigation · 2026
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Lynnette Wei Hsien KohNeuro-Oncology Research Laboratory, Department of Research, National Neuroscience Institute, Singapore, Singapore.
Qing You PangNeuro-Oncology Research Laboratory, Department of Research, National Neuroscience Institute, Singapore, Singapore.
Wisna NoveraNeuro-Oncology Research Laboratory, Department of Research, National Neuroscience Institute, Singapore, Singapore.
See Wee LimNeuro-Oncology Research Laboratory, Department of Research, National Neuroscience Institute, Singapore, Singapore.
Yuk Kien ChongNeuro-Oncology Research Laboratory, Department of Research, National Neuroscience Institute, Singapore, Singapore.
Jinyue LiuLaboratory of Single-Cell Spatial Neuromics, Genome Institute of Singapore, Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
Samantha Ya Lyn AngDepartment of Neurosurgery, National Neuroscience Institute, Singapore, Singapore.
Ron Weng Yee LohEnabling Village, SG Enable, Singapore, Singapore.
Huilin ShaoInstitute for Health Innovation & Technology, National University of Singapore, Singapore, Singapore.
Jianhong ChingCardiovascular & Metabolic Disorders Program, Duke-National University of Singapore Medical School, Singapore, Singapore.
Yulan WangSingapore Phenome Centre, Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore.
Stephen YipDepartment of Pathology and Laboratory Medicine, The University of British Columbia, Vancouver, British Columbia, Canada.ORCID 0000-0002-8514-9861
Patrick TanCancer and Stem Cell Biology Program, Duke-National University of Singapore Medical School, Singapore, Singapore.
Shang LiCancer and Stem Cell Biology Program, Duke-National University of Singapore Medical School, Singapore, Singapore.
David Chyi Yeu LowDepartment of Neurosurgery, National Neuroscience Institute, Singapore, Singapore.
Anne PhelanBenevolentAI, London, UK.
Gabriel RosserBenevolentAI, London, UK.
Nguan Soon TanLee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore.ORCID 0000-0003-0136-7341
Carol TangNeuro-Oncology Research Laboratory, Department of Research, National Neuroscience Institute, Singapore, Singapore.ORCID 0000-0002-1835-5083
Beng Ti AngNeuro-Oncology Research Laboratory, Department of Research, National Neuroscience Institute, Singapore, Singapore.

Funding

National Research Foundation Singapore MOH-000541-00Singapore Ministry of Health's National Medical Research Council NMRC/CIRG/1441/2016
6 · The paper itself

Abstract

backgroundEnhancer of zeste homolog 2 (EZH2), well known for its canonical methyltransferase activity in transcriptional repression in many cancers including glioblastoma (GBM), has an understudied noncanonical 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 su(var)3-9, enhancer-of-zeste and trithorax domain show limited efficacy and lack durable response, suggesting that underlying differences in the noncanonical pathway may yield new knowledge. Here, we unveiled dual roles of the EZH2 CXC domain in therapeutically distinct, reactive oxygen species (ROS)-stratified tumors.

methodsWe 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.

resultsIn ROS(+) tumors, CXC-mediated co-interaction with RelB drives constitutive activation of noncanonical NF-κB2 signaling, sustaining the ROS(+) chemoresistant phenotype. In contrast, in ROS(-) subtypes, Polycomb Repressive Complex 2 methyltransferase activity represses canonical NF-κB. Addressing the lack of EZH2inh targeting its nonmethyltransferase roles, we utilized a brain-penetrant NIKinh that disrupts EZH2-RelB binding, consequently prolonging survival in orthotopic ROS(+)-implanted mice.

conclusionsOur 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 noncanonical activities and underscoring the significance of patient stratification methodologies.

Indexed as

Brain NeoplasmsEnhancer of Zeste Homolog 2 ProteinGlioblastomaReactive Oxygen SpeciesAnimalsCell ProliferationGene Expression Regulation, NeoplasticHumansMiceTumor Cells, CulturedXenograft Model Antitumor AssaysEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanReactive Oxygen Speciesbrain cancerEZH2glioblastomapatient stratificationprecision medicine

Identifiers

PMID39373211
PMCPMC11812038

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.