Evidence map›Paper›PMID 39020166›Full record

ArticleNature2024

In vivo single-cell CRISPR uncovers distinct TNF programmes in tumour evolution.

Peter F Renz, Umesh Ghoshdastider, Simona Baghai Sain, Fabiola Valdivia-Francia, Ameya Khandekar, Mark Ormiston, Martino Bernasconi, Clara Duré, Jonas A Kretz, Minkyoung Lee and 7 more

Abstract read
In one paragraph

Article in Nature, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

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  20. Identification of a conserved RNA structure in thebioRxiv : the preprint server for biology · 2025
    Article
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

17 authors.

Peter F Renz *Institute for Regenerative Medicine (IREM), University of Zurich, Schlieren-Zurich, Switzerland.ORCID 0009-0007-7259-5022
Umesh Ghoshdastider *Institute for Regenerative Medicine (IREM), University of Zurich, Schlieren-Zurich, Switzerland.
Simona Baghai Sain *Department of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.ORCID 0000-0002-2357-7027
Fabiola Valdivia-FranciaInstitute for Regenerative Medicine (IREM), University of Zurich, Schlieren-Zurich, Switzerland.
Ameya KhandekarMax Perutz Labs, Vienna BioCenter Campus (VBC), Vienna, Austria.
Mark OrmistonInstitute for Regenerative Medicine (IREM), University of Zurich, Schlieren-Zurich, Switzerland.
Martino BernasconiInstitute for Regenerative Medicine (IREM), University of Zurich, Schlieren-Zurich, Switzerland.ORCID 0000-0001-6581-7001
Clara DuréInstitute for Regenerative Medicine (IREM), University of Zurich, Schlieren-Zurich, Switzerland.
Jonas A KretzDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.ORCID 0000-0003-4023-4103
Minkyoung LeeDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.
Katie HyamsInstitute for Regenerative Medicine (IREM), University of Zurich, Schlieren-Zurich, Switzerland.
Merima FornyInstitute for Regenerative Medicine (IREM), University of Zurich, Schlieren-Zurich, Switzerland.
Marcel PohlyDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.ORCID 0000-0003-0393-5840
Xenia FichtDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.ORCID 0000-0002-4534-8225
Stephanie J EllisMax Perutz Labs, Vienna BioCenter Campus (VBC), Vienna, Austria.
Andreas E MoorDepartment of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland. andreas.moor@bsse.ethz.ch.ORCID 0000-0001-8715-8449
Ataman SendoelInstitute for Regenerative Medicine (IREM), University of Zurich, Schlieren-Zurich, Switzerland. ataman.sendoel@uzh.ch.ORCID 0000-0002-0381-9965

Funding

European Research CouncilEuropean Union′s Horizon 2020 research and innovation programmeNational Center of Competence in Research (NCCR) on RNA and DiseaseSwiss Cancer Research foundation
6 · The paper itself

Abstract

The tumour evolution model posits that malignant transformation is preceded by randomly distributed driver mutations in cancer genes, which cause clonal expansions in phenotypically normal tissues. Although clonal expansions can remodel entire tissues

Indexed as

Carcinoma, Squamous CellCell Transformation, NeoplasticClonal EvolutionClone CellsCRISPR-Cas SystemsSingle-Cell AnalysisTumor Necrosis FactorsAnimalsAutocrine CommunicationClustered Regularly Interspaced Short Palindromic RepeatsEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansMacrophagesMaleReceptors, Tumor Necrosis Factor, Type ITumor Necrosis Factors

Identifiers

PMID39020166
PMCPMC11306103

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.