Evidence map›Paper›PMID 41723269›Full record

ArticleCommunications biology2026

PRC2 loss impairs small cell lung cancer tumorigenesis and enhances sensitivity to G9a/GLP inhibition.

Jawahar Kopparam, Gayathri Chandrasekaran, Danielle Hulsman, Liesa-Marie Pilger, Karen Stevers, Ji-Ying Song, Miguel Hernandez-Quiles, Jelmer Dijkstra, Jitendra Badhai, Nick Landman and 2 more

Abstract read
In one paragraph

Article in Communications biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Jawahar Kopparam *Division of Molecular Genetics, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, the Netherlands.
Gayathri Chandrasekaran *Division of Molecular Genetics, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, the Netherlands.
Danielle HulsmanDivision of Molecular Genetics, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, the Netherlands.
Liesa-Marie PilgerDivision of Molecular Genetics, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, the Netherlands.ORCID http://orcid.org/0009-0005-1448-790X
Karen SteversDivision of Molecular Genetics, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, the Netherlands.ORCID http://orcid.org/0009-0001-3306-5498
Ji-Ying SongDepartment of Experimental Animal Pathology, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, the Netherlands.
Miguel Hernandez-QuilesDivision of Molecular Genetics, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, the Netherlands.
Jelmer DijkstraDivision of Molecular Genetics, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, the Netherlands.
Jitendra BadhaiDivision of Molecular Genetics, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, the Netherlands.
Nick LandmanDivision of Molecular Genetics, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, the Netherlands.
Michiel VermeulenDivision of Molecular Genetics, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, the Netherlands.ORCID http://orcid.org/0000-0003-0836-6894
Maarten van LohuizenDivision of Molecular Genetics, The Netherlands Cancer Institute, Plesmanlaan 121, Amsterdam, the Netherlands. m.v.lohuizen@nki.nl.ORCID http://orcid.org/0000-0001-6877-2873

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Effective targeted therapies for small cell lung cancer (SCLC) remain a significant challenge. Targeting the epigenome to overcome immune evasion and chemoresistance represents a promising strategy to improve treatment outcomes. In this study, we explored the role of Polycomb repressive complex 2 (PRC2), a key transcriptional repressor, by dissecting its structural and enzymatic functions. Conditional deletion of Eed, a core structural component of PRC2, prevented tumor formation in an autochthonous SCLC model. In contrast, enzymatic inhibition of EZH2 had no impact on tumor growth but significantly altered the PRC2 interactome, unveiling novel targets for drug development. Since EZH2 inhibitors are already clinically approved for other cancers, we conducted a focused combination drug screen to enhance their therapeutic potential in SCLC. Our findings revealed that prolonged EZH2 inhibition sensitized neuroendocrine cancer cells to G9a/GLP inhibition. Transcriptomic analysis revealed that the drug combination triggered an oxidative stress response by modulating the expression of cellular oxidases, an effect that could be reversed by antioxidant treatment. These results underscore the critical role of PRC2's structural functions in SCLC and identify promising drug combinations to enhance the efficacy of EZH2 inhibitors.

Indexed as

CarcinogenesisHistocompatibility AntigensHistone-Lysine N-MethyltransferaseLung NeoplasmsPolycomb Repressive Complex 2Small Cell Lung CarcinomaAnimalsCell Line, TumorEnhancer of Zeste Homolog 2 ProteinGene Expression Regulation, NeoplasticHumansMiceEHMT2 protein, humanEnhancer of Zeste Homolog 2 ProteinHistocompatibility AntigensHistone-Lysine N-MethyltransferasePolycomb Repressive Complex 2

Identifiers

PMID41723269
PMCPMC13035885

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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.