Evidence map›Paper›PMID 36550208›Full record

ArticleBritish journal of cancer2023

The Neuropilin-1/PKC axis promotes neuroendocrine differentiation and drug resistance of prostate cancer.

Charly Blanc, Anissa Moktefi, Ariane Jolly, Pierre de la Grange, Denise Gay, Nathalie Nicolaiew, Fannie Semprez, Pascale Maillé, Pascale Soyeux, Virginie Firlej and 9 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 15% of its field
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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Androgen Signaling in Prostate Cancer: When a Friend Turns Foe.Endocrine, metabolic & immune disorders drug targets · 2025
    Review
  6. Article
  7. Review
  8. Review
  9. Targeting Key Players of Neuroendocrine Differentiation in Prostate Cancer.International journal of molecular sciences · 2023
    Review
  10. Review
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

19 authors at 5 institutions in 2 countries.

Charly BlancUniv Paris Est Creteil, INSERM, IMRB, 94010, Creteil, France.
Anissa MoktefiUniv Paris Est Creteil, INSERM, IMRB, 94010, Creteil, France.ORCID 0000-0002-6015-3979
Ariane JollyGenosplice®, IM, Hôpital Pitié-Salpêtrière, Paris, France.
Pierre de la GrangeGenosplice®, IM, Hôpital Pitié-Salpêtrière, Paris, France.
Denise GayDLGBiologics, 75017, Paris, France.
Nathalie NicolaiewUniv Paris Est Creteil, INSERM, IMRB, 94010, Creteil, France.
Fannie SemprezUniv Paris Est Creteil, INSERM, IMRB, 94010, Creteil, France.
Pascale MailléUniv Paris Est Creteil, INSERM, IMRB, 94010, Creteil, France.
Pascale SoyeuxUniv Paris Est Creteil, INSERM, IMRB, 94010, Creteil, France.
Virginie FirlejUniv Paris Est Creteil, INSERM, IMRB, 94010, Creteil, France.
Francis VacherotUniv Paris Est Creteil, INSERM, IMRB, 94010, Creteil, France.
Damien DestouchesUniv Paris Est Creteil, INSERM, IMRB, 94010, Creteil, France.
Mohamed AmicheUniv Paris Est Creteil, INSERM, IMRB, 94010, Creteil, France.
Stéphane TerryFaculty of Medicine, University Paris-Saclay, Le Kremlin-Bicêtre, France.
Alexandre de la TailleUniv Paris Est Creteil, INSERM, IMRB, 94010, Creteil, France.
Arturo Londoño-VallejoInstitut Curie, PSL Research University, CNRS UMR 3244, 75005, Paris, France.ORCID 0000-0003-3535-7563
Yves AlloryUniv Paris Est Creteil, INSERM, IMRB, 94010, Creteil, France.
Jean DelbéUniv Paris Est Creteil, INSERM, IMRB, 94010, Creteil, France.
Yamina Hamma-KourbaliUniv Paris Est Creteil, INSERM, IMRB, 94010, Creteil, France. hamma@u-pec.fr.ORCID 0000-0002-2754-8928
Inserm · FRCentre National de la Recherche Scientifique · FRSorbonne Université · FRHeidelberg University · DEUniversité Paris-Saclay · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeuroendocrine prostate cancer (NEPC) is a multi-resistant variant of prostate cancer (PCa) that has become a major challenge in clinics. Understanding the neuroendocrine differentiation (NED) process at the molecular level is therefore critical to define therapeutic strategies that can prevent multi-drug resistance.

methodsUsing RNA expression profiling and immunohistochemistry, we have identified and characterised a gene expression signature associated with the emergence of NED in a large PCa cohort, including 169 hormone-naïve PCa (HNPC) and 48 castration-resistance PCa (CRPC) patients. In vitro and preclinical in vivo NED models were used to explore the cellular mechanism and to characterise the effects of castration on PCa progression.

resultsWe show for the first time that Neuropilin-1 (NRP1) is a key component of NED in PCa cells. NRP1 is upregulated in response to androgen deprivation therapies (ADT) and elicits cell survival through induction of the PKC pathway. Downmodulation of either NRP1 protein expression or PKC activation suppresses NED, prevents tumour evolution toward castration resistance and increases the efficacy of docetaxel-based chemotherapy in preclinical models in vivo.

conclusionsThis study reveals the NRP1/PKC axis as a promising therapeutic target for the prevention of neuroendocrine castration-resistant variants of PCa and indicates NRP1 as an early transitional biomarker.

Indexed as

Prostatic NeoplasmsProstatic Neoplasms, Castration-ResistantAndrogen AntagonistsCell DifferentiationCell Line, TumorDrug ResistanceHumansMaleNeuropilin-1Androgen AntagonistsNeuropilin-1

Identifiers

PMID36550208
PMCPMC9977768
OpenAlexW4312114780

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.