Evidence map›Paper›PMID 31855178›Full record

ArticleeLife2019

TLE3 loss confers AR inhibitor resistance by facilitating GR-mediated human prostate cancer cell growth.

Sander Al Palit, Daniel Vis, Suzan Stelloo, Cor Lieftink, Stefan Prekovic, Elise Bekers, Ingrid Hofland, Tonći Šuštić, Liesanne Wolters, Roderick Beijersbergen and 5 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
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  5. LBFextract: Unveiling transcription factor dynamics from liquid biopsy data.Computational and structural biotechnology journal · 2024
    Article
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  19. Review
  20. CRISPR Screen Contributes to Novel Target Discovery in Prostate Cancer.International journal of molecular sciences · 2021
    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

15 authors at 2 institutions in 2 countries.

Sander Al PalitDivision of Molecular Carcinogenesis, Netherlands Cancer Institute, Amsterdam, Netherlands.ORCID 0000-0003-2487-4311
Daniel VisDivision of Molecular Carcinogenesis, Netherlands Cancer Institute, Amsterdam, Netherlands.
Suzan StellooDivision of Oncogenomics, Oncode Institute, Netherlands Cancer Institute, Amsterdam, Netherlands.
Cor LieftinkDivision of Molecular Carcinogenesis, Netherlands Cancer Institute, Amsterdam, Netherlands.
Stefan PrekovicDivision of Oncogenomics, Oncode Institute, Netherlands Cancer Institute, Amsterdam, Netherlands.
Elise BekersDivision of Pathology, Netherlands Cancer Institute, Amsterdam, Netherlands.
Ingrid HoflandCore Facility Molecular Pathology & Biobanking, Netherlands Cancer Institute, Amsterdam, Netherlands.
Tonći ŠuštićDivision of Molecular Carcinogenesis, Netherlands Cancer Institute, Amsterdam, Netherlands.
Liesanne WoltersDivision of Molecular Carcinogenesis, Netherlands Cancer Institute, Amsterdam, Netherlands.
Roderick BeijersbergenDivision of Molecular Carcinogenesis, Netherlands Cancer Institute, Amsterdam, Netherlands.
Andries M BergmanDepartment of Medical Oncology, Netherlands Cancer Institute, Amsterdam, Netherlands.
Balázs GyőrffyDepartment of Bioinformatics, Semmelweis University, Budapest, Hungary.
Lodewyk Fa WesselsDivision of Molecular Carcinogenesis, Netherlands Cancer Institute, Amsterdam, Netherlands.
Wilbert ZwartDivision of Oncogenomics, Oncode Institute, Netherlands Cancer Institute, Amsterdam, Netherlands.ORCID 0000-0002-9823-7289
Michiel S van der HeijdenDivision of Molecular Carcinogenesis, Netherlands Cancer Institute, Amsterdam, Netherlands.
The Netherlands Cancer Institute · NLSemmelweis University · HU

Funding

KWF Kankerbestrijding Alpe d'HuZes Bas Mulder AwardKWF Kankerbestrijding NKI2014-7080NWO VIDI grant
6 · The paper itself

Abstract

Androgen receptor (AR) inhibitors represent the mainstay of prostate cancer treatment. In a genome-wide CRISPR-Cas9 screen using LNCaP prostate cancer cells, loss of co-repressor

Indexed as

Androgen Receptor AntagonistsBenzamidesCell Line, TumorCell ProliferationCo-Repressor ProteinsCRISPR-Cas SystemsDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHEK293 CellsHepatocyte Nuclear Factor 3-alphaHumansMaleNitrilesPhenylthiohydantoinProstateProstatic NeoplasmsAndrogen Receptor AntagonistsBenzamidesCo-Repressor ProteinsenzalutamideFOXA1 protein, humanHepatocyte Nuclear Factor 3-alphaNitrilesPhenylthiohydantoinReceptors, AndrogenReceptors, GlucocorticoidTLE3 protein, humanandrogen receptorcancer biologyEnzalutamideglucocorticoid receptorhumanprostate cancertherapy resistanceTLE3

Identifiers

PMID31855178
PMCPMC6968917
OpenAlexW2996645789

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.