Evidence map›Paper›PMID 32313004›Full record

ArticleNature communications2020

Genetic characterization of a unique neuroendocrine transdifferentiation prostate circulating tumor cell-derived eXplant model.

Vincent Faugeroux, Emma Pailler, Marianne Oulhen, Olivier Deas, Laura Brulle-Soumare, Céline Hervieu, Virginie Marty, Kamelia Alexandrova, Kiki C Andree, Nikolas H Stoecklein and 12 more

Abstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing 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

51 citing papers in PubMed.

  1. Article
  2. [Efficacy of CD4/TGF-β bispecific antibody in a mouse model of peritoneal metastasis of malignant melanoma].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
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  17. Clinical application of circulating tumor cells.Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V · 2023
    Article
  18. Article
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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

22 authors.

Vincent FaugerouxINSERM, U981 "Identification of Molecular Predictors and new Targets for Cancer Treatment", 94805, Villejuif, France.
Emma Pailler *INSERM, U981 "Identification of Molecular Predictors and new Targets for Cancer Treatment", 94805, Villejuif, France.ORCID http://orcid.org/0000-0002-7329-7429
Marianne Oulhen *Gustave Roussy, Université Paris-Saclay, "Circulating Tumor Cells" Translational Platform, CNRS UMS3655-INSERM US23 AMMICA, 94805, Villejuif, France.
Olivier Deas *XenTech, 91000, Evry, France.
Laura Brulle-SoumareXenTech, 91000, Evry, France.ORCID http://orcid.org/0000-0003-3371-2496
Céline HervieuINSERM, U981 "Identification of Molecular Predictors and new Targets for Cancer Treatment", 94805, Villejuif, France.
Virginie MartyGustave Roussy, Université Paris-Saclay, Experimental and Translational Pathology Platform, CNRS UMS3655-INSERM US23 AMMICA, 94805, Villejuif, France.
Kamelia AlexandrovaGustave Roussy, Université Paris-Saclay, Department of Cell Therapy, 94805, Villejuif, France.
Kiki C AndreeMedical Cell Biophysics Group, Technical Medical Centre, Faculty of Science and Technology, University of Twente, 7522 NB, Enschede, The Netherlands.ORCID http://orcid.org/0000-0002-7807-6289
Nikolas H StoeckleinDepartment of General, Visceral and Pediatric Surgery, Medical Faculty, University Hospital of the Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.ORCID http://orcid.org/0000-0002-3412-594X
Dominique TramalloniGustave Roussy, Université Paris-Saclay, Department of Cell Therapy, 94805, Villejuif, France.
Stefano CairoXenTech, 91000, Evry, France.ORCID http://orcid.org/0000-0002-4725-5970
Maud NgoCamusGustave Roussy, Université Paris-Saclay, Department of Cancer Medicine, 94805, Villejuif, France.
Claudio NicotraGustave Roussy, Université Paris-Saclay, Department of Cancer Medicine, 94805, Villejuif, France.
Leon W M M TerstappenMedical Cell Biophysics Group, Technical Medical Centre, Faculty of Science and Technology, University of Twente, 7522 NB, Enschede, The Netherlands.ORCID http://orcid.org/0000-0001-5944-3787
Nicolo ManaresiMenarini Silicon Biosystems S.p.A, 40013, Bologna, Italy.ORCID http://orcid.org/0000-0002-1681-7037
Valérie LapierreGustave Roussy, Université Paris-Saclay, Department of Cell Therapy, 94805, Villejuif, France.
Karim FizaziINSERM, U981 "Identification of Molecular Predictors and new Targets for Cancer Treatment", 94805, Villejuif, France.
Jean-Yves ScoazecGustave Roussy, Université Paris-Saclay, Experimental and Translational Pathology Platform, CNRS UMS3655-INSERM US23 AMMICA, 94805, Villejuif, France.ORCID http://orcid.org/0000-0003-1604-6823
Yohann LoriotGustave Roussy, Université Paris-Saclay, Department of Cancer Medicine, 94805, Villejuif, France. Yohann.loriot@gustaveroussy.fr.
Jean-Gabriel JuddeXenTech, 91000, Evry, France.
Françoise FaraceINSERM, U981 "Identification of Molecular Predictors and new Targets for Cancer Treatment", 94805, Villejuif, France. francoise.farace@gustaveroussy.fr.ORCID http://orcid.org/0000-0001-8563-160X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transformation of castration-resistant prostate cancer (CRPC) into an aggressive neuroendocrine disease (CRPC-NE) represents a major clinical challenge and experimental models are lacking. A CTC-derived eXplant (CDX) and a CDX-derived cell line are established using circulating tumor cells (CTCs) obtained by diagnostic leukapheresis from a CRPC patient resistant to enzalutamide. The CDX and the derived-cell line conserve 16% of primary tumor (PT) and 56% of CTC mutations, as well as 83% of PT copy-number aberrations including clonal TMPRSS2-ERG fusion and NKX3.1 loss. Both harbor an androgen receptor-null neuroendocrine phenotype, TP53, PTEN and RB1 loss. While PTEN and RB1 loss are acquired in CTCs, evolutionary analysis suggest that a PT subclone harboring TP53 loss is the driver of the metastatic event leading to the CDX. This CDX model provides insights on the sequential acquisition of key drivers of neuroendocrine transdifferentiation and offers a unique tool for effective drug screening in CRPC-NE management.

Indexed as

AnimalsBenzamidesCarcinoma, NeuroendocrineCell Line, TumorCell TransdifferentiationDisease Models, AnimalDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHomeodomain ProteinsHumansMaleMiceMice, Inbred NODNeoplastic Cells, CirculatingNitrilesPhenylthiohydantoinBenzamidesenzalutamideHomeodomain ProteinsNitrilesNKX3-1 protein, humanPhenylthiohydantoinReceptors, AndrogenSerine EndopeptidasesTMPRSS2 protein, humanTP53 protein, humanTranscription FactorsTumor Suppressor Protein p53

Identifiers

PMID32313004
PMCPMC7171138

What OpenQuestion holds

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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.