Evidence map›Paper›PMID 42086671›Full record

ArticleBritish journal of cancer2026

Changes in Cyclin E1 expression and CCNE1 amplification in high-grade ovarian carcinomas post-PARP inhibitor exposure.

Alexis Trecourt, Alexander Valent, Elisa Yaniz-Galende, Etienne Rouleau, Juan Francisco Grau Bejar, Félix Blanc-Durand, Elodie Edmond, Audrey Le Formal, Catherine Genestie, Alexandra Leary

Abstract read
In one paragraph

Article in British journal of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Alexis TrecourtHospices Civils de Lyon, Centre Hospitalier Lyon-Sud, Service de Pathologie Multi-Site, Lyon, France.ORCID http://orcid.org/0000-0002-1674-1888
Alexander ValentGustave Roussy, Laboratoire de cytogénétique, Villejuif, France.
Elisa Yaniz-GalendeInstitut National de la Santé et de la Recherche Médicale (INSERM) U981, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
Etienne RouleauInstitut National de la Santé et de la Recherche Médicale (INSERM) U981, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
Juan Francisco Grau BejarInstitut National de la Santé et de la Recherche Médicale (INSERM) U981, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
Félix Blanc-DurandInstitut National de la Santé et de la Recherche Médicale (INSERM) U981, Gustave Roussy, Université Paris-Saclay, Villejuif, France.ORCID http://orcid.org/0000-0002-5277-1515
Elodie EdmondGustave Roussy, Plateforme de pathologie expérimentale et translationnelle (PETRA), INSERM US23/CNRS UAR3655, Villejuif, France.
Audrey Le FormalInstitut National de la Santé et de la Recherche Médicale (INSERM) U981, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
Catherine GenestieInstitut National de la Santé et de la Recherche Médicale (INSERM) U981, Gustave Roussy, Université Paris-Saclay, Villejuif, France.
Alexandra LearyInstitut National de la Santé et de la Recherche Médicale (INSERM) U981, Gustave Roussy, Université Paris-Saclay, Villejuif, France. Alexandra.LEARY@gustaveroussy.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTherapeutic options are limited for patients with high-grade ovarian carcinoma (HGOC) progressing after poly(adenosine diphosphate-ribose) polymerase-inhibitor (PARPi). WEE1/CDK2-inhibitors efficacy is under investigation in HGOC harbouring CCNE1 amplification/Cyclin E1 overexpression. However, Cyclin E1 expression evolution after PARPi has not been studied. We aimed to describe Cyclin E1 expression/CCNE1 copy number in post-PARPi HGOC samples and compare to paired samples from diagnosis and/or post-neoadjuvant chemotherapy (post-NACT).

methodsThirty-eight patients with available post-PARPi samples were included; paired samples from diagnosis (n = 26) and/or post-NACT (n = 24) were collected. Cyclin E1 expression was quantified using immunohistochemistry (IHC). CCNE1 copy number was evaluated using fluorescent in situ hybridisation (FISH).

resultsSeventy-two percent (26/36) of HGOC were homologous recombination deficient. Intratumoral Cyclin E1 expression was homogenous in samples from synchronous but anatomically distinct tumour sites. However, Cyclin E1 expression increased significantly between diagnosis and progression post-PARPi (median H-score = 113 versus 163, respectively; p = 0.034). The proportion of Cyclin E1-high (H-score ≥ 150) tumours was 31% (8/26) at diagnosis, 42% (10/24) post-NACT, and increased significantly to 61% (23/38) post-PARPi (versus diagnosis; p = 0.024). In contrast, only 10% (2/20) of Cyclin E1-high HGOC exhibited CCNE1 amplification ( ≥ 8 CCNE1 copies).

conclusionsCyclin E1 expression in HGOC increases at post-PARPi progression, independently of CCNE1 amplification.

Indexed as

Cyclin EOncogene ProteinsOvarian NeoplasmsPoly(ADP-ribose) Polymerase InhibitorsAdultAgedFemaleGene AmplificationHumansIn Situ Hybridization, FluorescenceMiddle AgedNeoplasm GradingCCNE1 protein, humanCyclin EOncogene ProteinsPoly(ADP-ribose) Polymerase Inhibitors

Identifiers

PMID42086671
PMCPMC13373207

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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.