EZH2 functional dichotomy in reactive oxygen species-stratified glioblastoma

Lynnette Wei Hsien Koh 1, 2
Qing You Pang 1, 2
Wisna Novera 1, 2
See Wee Lim 1, 2
Yuk Kien Chong 1, 2
Jinyue Liu 3, 4
Samantha Ya Lyn Ang 5, 6, 7, 8
Ron Weng Yee Loh 9, 10
Huilin Shao 11, 12, 13, 14, 15, 16, 17, 18
Jianhong Ching 19, 20, 21, 22
Yulan Wang 23, 24
Stephen Yip 25, 26
PATRICK TAN 27, 28, 29, 30, 31, 32, 33, 34
Shang Li 27, 30, 31, 34
David Chyi Yeu Low 5, 6, 7, 8
Anne Phelan 35
Gabriel Rosser 35
Nguan Soon Tan 36, 37, 38, 39
Carol Tang 1, 2, 9, 10, 27, 31
Beng Ti Ang 1, 2, 5, 6, 7, 8
2
 
Neuro-Oncology Research Laboratory, Department of Research, National Neuroscience Institute , Singapore ,
7
 
National Neuroscience Institute Department of Neurosurgery, , Singapore ,
9
 
Enabling Village , SG Enable,
10
 
Enabling Village, SG Enable , Singapore ,
20
 
KK Research Centre , KK Women’s and Children’s Hospital,
22
 
KK Research Centre, KK Women’s and Children’s Hospital , Singapore ,
35
 
BenevolentAI , London ,
37
 
School of Biological Sciences , Nanyang Technological University,
Publication typeJournal Article
Publication date2024-10-07
scimago Q1
wos Q1
SJR6.974
CiteScore30.2
Impact factor13.4
ISSN15228517, 15235866
Abstract
Background

Enhancer 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.

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 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.

Conclusions

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 noncanonical activities and underscoring the significance of patient stratification methodologies.

Found 
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GOST |
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GOST Copy
Koh L. W. H. et al. EZH2 functional dichotomy in reactive oxygen species-stratified glioblastoma // Neuro-Oncology. 2024.
GOST all authors (up to 50) Copy
Koh L. W. H. et al. EZH2 functional dichotomy in reactive oxygen species-stratified glioblastoma // Neuro-Oncology. 2024.
RIS |
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RIS Copy
TY - JOUR
DO - 10.1093/neuonc/noae206
UR - https://academic.oup.com/neuro-oncology/advance-article/doi/10.1093/neuonc/noae206/7814577
TI - EZH2 functional dichotomy in reactive oxygen species-stratified glioblastoma
T2 - Neuro-Oncology
AU - Koh, Lynnette Wei Hsien
AU - Pang, Qing You
AU - Novera, Wisna
AU - Lim, See Wee
AU - Chong, Yuk Kien
AU - Liu, Jinyue
AU - Ang, Samantha Ya Lyn
AU - Loh, Ron Weng Yee
AU - Shao, Huilin
AU - Ching, Jianhong
AU - Wang, Yulan
AU - Yip, Stephen
AU - TAN, PATRICK
AU - Li, Shang
AU - Low, David Chyi Yeu
AU - Phelan, Anne
AU - Rosser, Gabriel
AU - Tan, Nguan Soon
AU - Tang, Carol
AU - Beng Ti Ang
PY - 2024
DA - 2024/10/07
PB - Oxford University Press
PMID - 39373211
SN - 1522-8517
SN - 1523-5866
ER -
BibTex
Cite this
BibTex (up to 50 authors) Copy
@article{2024_Koh,
author = {Lynnette Wei Hsien Koh and Qing You Pang and Wisna Novera and See Wee Lim and Yuk Kien Chong and Jinyue Liu and Samantha Ya Lyn Ang and Ron Weng Yee Loh and Huilin Shao and Jianhong Ching and Yulan Wang and Stephen Yip and PATRICK TAN and Shang Li and David Chyi Yeu Low and Anne Phelan and Gabriel Rosser and Nguan Soon Tan and Carol Tang and Beng Ti Ang and others},
title = {EZH2 functional dichotomy in reactive oxygen species-stratified glioblastoma},
journal = {Neuro-Oncology},
year = {2024},
publisher = {Oxford University Press},
month = {oct},
url = {https://academic.oup.com/neuro-oncology/advance-article/doi/10.1093/neuonc/noae206/7814577},
doi = {10.1093/neuonc/noae206}
}