Evidence map›Paper›PMID 42777032›Full record

ArticleScience advances2026

Persistent TOP1 cleavage complexes in drug-tolerant cells drive adaptive resistance to EGFR-targeted therapies in lung cancer.

Mathéa Geraud, Remi Gence, Anne Casanova, Estelle Taranchon-Clermont, Simona Salimbeni, Nesibe Özsu, Maina Vienne, Célia Delahaye, Elodie Borrull, Amélie Lusque and 10 more

Abstract read
In one paragraph

Article in Science advances, 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

20 authors.

Mathéa GeraudUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.ORCID 0009-0000-6879-0588
Remi GenceUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.ORCID 0000-0003-0747-3540
Anne CasanovaUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.
Estelle Taranchon-ClermontUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.
Simona SalimbeniUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.
Nesibe ÖzsuUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.
Maina VienneUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.
Célia DelahayeUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.ORCID 0009-0004-7966-5597
Elodie BorrullUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.
Amélie LusqueUniversity of Toulouse, Oncopole Claudius Regaud, IUCT-Oncopole, Biostatistics & Health Data Science Unit, Toulouse, France.ORCID 0000-0001-9691-5536
Mathilde MorisseauUniversity of Toulouse, Oncopole Claudius Regaud, IUCT-Oncopole, Biostatistics & Health Data Science Unit, Toulouse, France.
Thomas FilleronUniversity of Toulouse, Oncopole Claudius Regaud, IUCT-Oncopole, Biostatistics & Health Data Science Unit, Toulouse, France.
Delphine PaganUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.ORCID 0000-0002-8298-3682
Camille TahaUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.
Agnese CristiniUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.ORCID 0000-0003-0235-8770
Julien MazièresUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.ORCID 0000-0002-5921-7613
Olivier CalvayracUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.ORCID 0000-0002-0908-8323
Gilles FavreUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.ORCID 0000-0002-2344-1883
Anne PradinesUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.ORCID 0000-0002-2449-678X
Olivier SordetUniversity of Toulouse, CNRS, INSERM, CRCT, Toulouse, France.ORCID 0000-0001-6027-4925

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Resistance to targeted cancer therapies often arises from drug-tolerant cells, which survive treatment by entering a nonproliferative state. Over time, these cells can acquire mutations that contribute to cell reproliferation, but how nonproliferating drug-tolerant cells accumulate these mutations remains unclear. Here, we show that EGFR inhibition in

Indexed as

DNA Topoisomerases, Type IDrug Resistance, NeoplasmLung NeoplasmsAnimalsCell Line, TumorErbB ReceptorsHumansMutationPhosphoric Diester HydrolasesReactive Oxygen SpeciesTopotecanDNA Topoisomerases, Type IEGFR protein, humanErbB ReceptorsPhosphoric Diester HydrolasesReactive Oxygen SpeciesTDP1 protein, humanTOP1 protein, humanTopotecan

Identifiers

PMID42777032
PMCPMC13600163

What Socratic holds

Textmetadata
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 Socratic graph.