Evidence map›Paper›PMID 36451039›Full record

ReviewNature reviews. Urology2023

Experimental in vitro, ex vivo and in vivo models in prostate cancer research.

Verena Sailer, Gunhild von Amsberg, Stefan Duensing, Jutta Kirfel, Verena Lieb, Eric Metzger, Anne Offermann, Klaus Pantel, Roland Schuele, Helge Taubert and 4 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Urology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
9.0field-weighted citation impact, top 1% 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

37 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Ferroptosis in gastrointestinal stromal tumors.Journal of gastrointestinal oncology · 2026
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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

14 authors at 6 institutions in 1 country.

Verena SailerInstitute for Pathology, University Hospital Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.
Gunhild von AmsbergDepartment of Oncology and Hematology, University Cancer Center Hamburg Eppendorf and Martini-Klinik, Prostate Cancer Center, University Hospital Hamburg Eppendorf, Hamburg, Germany.
Stefan DuensingSection of Molecular Urooncology, Department of Urology, University Hospital Heidelberg and National Center for Tumour Diseases, Heidelberg, Germany.
Jutta KirfelInstitute for Pathology, University Hospital Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.
Verena LiebResearch Division Molecular Urology, Department of Urology and Paediatric Urology, University Hospital Erlangen, Erlangen, Germany.
Eric MetzgerDepartment of Urology, Center for Clinical Research, University of Freiburg Medical Center, Freiburg, Germany.
Anne OffermannInstitute for Pathology, University Hospital Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.
Klaus PantelInstitute for Tumour Biology, Center for Experimental Medicine, University Clinics Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0001-5736-2772
Roland SchueleDepartment of Urology, Center for Clinical Research, University of Freiburg Medical Center, Freiburg, Germany.
Helge TaubertResearch Division Molecular Urology, Department of Urology and Paediatric Urology, University Hospital Erlangen, Erlangen, Germany.
Sven WachResearch Division Molecular Urology, Department of Urology and Paediatric Urology, University Hospital Erlangen, Erlangen, Germany.
Sven PernerUniversity Hospital Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.
Stefan WernerInstitute for Tumour Biology, Center for Experimental Medicine, University Clinics Hamburg-Eppendorf, Hamburg, Germany.
Achim AignerClinical Pharmacology, Rudolf-Boehm-Institute for Pharmacology and Toxicology, University of Leipzig, Medical Faculty, Leipzig, Germany. achim.aigner@medizin.uni-leipzig.de.ORCID 0000-0002-2778-6256
University Hospital Schleswig-Holstein · DEUniversität Hamburg · DEUniversitätsklinikum Erlangen · DEUniversity of Freiburg · DEHeidelberg University · DELeipzig University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Androgen deprivation therapy has a central role in the treatment of advanced prostate cancer, often causing initial tumour remission before increasing independence from signal transduction mechanisms of the androgen receptor and then eventual disease progression. Novel treatment approaches are urgently needed, but only a fraction of promising drug candidates from the laboratory will eventually reach clinical approval, highlighting the demand for critical assessment of current preclinical models. Such models include standard, genetically modified and patient-derived cell lines, spheroid and organoid culture models, scaffold and hydrogel cultures, tissue slices, tumour xenograft models, patient-derived xenograft and circulating tumour cell eXplant models as well as transgenic and knockout mouse models. These models need to account for inter-patient and intra-patient heterogeneity, the acquisition of primary or secondary resistance, the interaction of tumour cells with their microenvironment, which make crucial contributions to tumour progression and resistance, as well as the effects of the 3D tissue network on drug penetration, bioavailability and efficacy.

Indexed as

Neoplastic Cells, CirculatingProstatic NeoplasmsAndrogen AntagonistsAnimalsDisease Models, AnimalHumansMaleMiceProstateTumor MicroenvironmentAndrogen Antagonists

Identifiers

PMID36451039
OpenAlexW4310415848

What OpenQuestion 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 OpenQuestion graph.