Evidence map›Paper›PMID 38450798›Full record

ReviewThe Prostate2024

Defining the challenges and opportunities for using patient-derived models in prostate cancer research.

W Nathaniel Brennen, Clémentine Le Magnen, Sofia Karkampouna, Nicolas Anselmino, Nathalie Bock, Nicholas Choo, Ashlee K Clark, Ilsa M Coleman, Robin Dolgos, Alison M Ferguson and 15 more

Abstract readReview
In one paragraph

Review in The Prostate, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

25 authors.

W Nathaniel BrennenDepartment of Oncology, Sidney Kimmel Comprehensive Cancer Center (SKCCC), Johns Hopkins University, Baltimore, Maryland, USA.ORCID 0000-0001-9807-7433
Clémentine Le MagnenInstitute of Medical Genetics and Pathology, University Hospital Basel, University of Basel, Basel, Switzerland.ORCID 0000-0002-6084-6054
Sofia KarkampounaUrology Research Laboratory, Department for BioMedical Research, University of Bern, Bern, Switzerland.
Nicolas AnselminoDepartment of Genitourinary Medical Oncology and the David H. Koch Center for Applied Research of Genitourinary Cancers, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Nathalie BockSchool of Biomedical Sciences at Translational Research Institute, Faculty of Health, Queensland University of Technology (QUT), Brisbane, QLD, Australia.
Nicholas ChooDepartment of Anatomy and Developmental Biology, Biomedicine Discovery Institute Cancer Program, Monash University, Clayton, VIC, Australia.
Ashlee K ClarkDepartment of Anatomy and Developmental Biology, Biomedicine Discovery Institute Cancer Program, Monash University, Clayton, VIC, Australia.
Ilsa M ColemanDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
Robin DolgosInstitute of Medical Genetics and Pathology, University Hospital Basel, University of Basel, Basel, Switzerland.ORCID 0009-0008-4699-3331
Alison M FergusonDepartment for BioMedical Research, University of Bern, Bern, Switzerland.
David L GoodePeter MacCallum Cancer Centre, Melbourne, VIC, Australia.
Marianna Krutihof-de JulioUrology Research Laboratory, Department for BioMedical Research, University of Bern, Bern, Switzerland.
Nora M NavoneDepartment of Genitourinary Medical Oncology and the David H. Koch Center for Applied Research of Genitourinary Cancers, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Peter S NelsonDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, Washington, USA.
Edward O'NeillNuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.ORCID 0000-0002-7987-8160
Laura H PorterDepartment of Anatomy and Developmental Biology, Biomedicine Discovery Institute Cancer Program, Monash University, Clayton, VIC, Australia.
Weranja RanasingheDepartment of Anatomy and Developmental Biology, Biomedicine Discovery Institute Cancer Program, Monash University, Clayton, VIC, Australia.
Takuro SunadaDepartment of Urology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Elizabeth D WilliamsSchool of Biomedical Sciences at Translational Research Institute, Faculty of Health, Queensland University of Technology (QUT), Brisbane, QLD, Australia.ORCID 0000-0002-3364-6655
Lisa M ButlerSouth Australian Immunogenomics Cancer Institute, University of Adelaide, Adelaide, SA, Australia.ORCID 0000-0003-2698-3220
Eva CoreyDepartment of Urology, University of Washington, Seattle, Washington, USA.ORCID 0000-0002-9244-3807
Wytske M van WeerdenDepartment of Urology, Erasmus Medical Center, Rotterdam, The Netherlands.ORCID 0000-0001-9916-5347
Renea A TaylorPeter MacCallum Cancer Centre, Melbourne, VIC, Australia.ORCID 0000-0003-2609-2380
Gail P RisbridgerDepartment of Anatomy and Developmental Biology, Biomedicine Discovery Institute Cancer Program, Monash University, Clayton, VIC, Australia.ORCID 0000-0003-3089-4028
Mitchell G LawrenceDepartment of Anatomy and Developmental Biology, Biomedicine Discovery Institute Cancer Program, Monash University, Clayton, VIC, Australia.ORCID 0000-0001-9520-3000

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI ALAN KEITH MEEKER · 1985 to 2026
$208.6M
TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETER S NELSON · 2002 to 2026
$58.1M
Steroid Metabolism in Castration-Resistant Prostate CancerP01CA163227 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI PETER S NELSON · 2013 to 2026
$25.0M
A First-in-Class FAP-activated Protoxin to disrupt the Tumor-Stroma Parasitic Cycle fueling lethal Prostate Cancer ProgressionR01CA255259 · NCI · JOHNS HOPKINS UNIVERSITY · PI BRENNEN, WILLIAM NATHANIEL · 2021 to 2025
$2.1M
Defining and Targeting Lineage Transition Programs Operative in AR Pathway Independent Prostate CancerR01CA234715 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI NELSON, PETER S · 2020 to 2024
$2.0M
Targeting Vulnerabilities Exposed by Cancer Treatment-Induced Lineage PlasticityR01CA266452 · NCI · FRED HUTCHINSON CANCER CENTER · PI PETER S NELSON · 2022 to 2026
$2.0M
Molecular features promoting sensitivity to LSD1i in castration-resistant prostate cancerR01CA279993 · NCI · JOHNS HOPKINS UNIVERSITY · PI William Nathaniel Brennen · 2024 to 2026
$1.8M
A Prostate Cancer Dependency Map to Identify Tumor Subtype-Specific VulnerabilitiesR21CA277368 · NCI · FRED HUTCHINSON CANCER CENTER · PI NELSON, PETER S · 2023 to 2024
$442k
NCI NIH HHS P01 CA163227NCI NIH HHS P30 CA006973NCI NIH HHS P30 CA015704NCI NIH HHS P50 CA097186NCI NIH HHS R01 CA234715NCI NIH HHS R01 CA255259NCI NIH HHS R01 CA266452NCI NIH HHS R01 CA279993NCI NIH HHS R21 CA277368Swiss National Science Foundation 310030_189149Swiss National Science Foundation 320030_205086Swiss National Science Foundation CRSII5_202297
6 · The paper itself

Abstract

backgroundThere are relatively few widely used models of prostate cancer compared to other common malignancies. This impedes translational prostate cancer research because the range of models does not reflect the diversity of disease seen in clinical practice. In response to this challenge, research laboratories around the world have been developing new patient-derived models of prostate cancer, including xenografts, organoids, and tumor explants.

methodsIn May 2023, we held a workshop at the Monash University Prato Campus for researchers with expertise in establishing and using a variety of patient-derived models of prostate cancer. This review summarizes our collective ideas on how patient-derived models are currently being used, the common challenges, and future opportunities for maximizing their usefulness in prostate cancer research.

resultsAn increasing number of patient-derived models for prostate cancer are being developed. Despite their individual limitations and varying success rates, these models are valuable resources for exploring new concepts in prostate cancer biology and for preclinical testing of potential treatments. Here we focus on the need for larger collections of models that represent the changing treatment landscape of prostate cancer, robust readouts for preclinical testing, improved in vitro culture conditions, and integration of the tumor microenvironment. Additional priorities include ensuring model reproducibility, standardization, and replication, and streamlining the exchange of models and data sets among research groups.

conclusionsThere are several opportunities to maximize the impact of patient-derived models on prostate cancer research. We must develop large, diverse and accessible cohorts of models and more sophisticated methods for emulating the intricacy of patient tumors. In this way, we can use the samples that are generously donated by patients to advance the outcomes of patients in the future.

Indexed as

Prostatic NeoplasmsHeterograftsHumansMaleOrganoidsProstateReproducibility of ResultsTumor Microenvironmentexplantsmodelsorganoidstumor microenvironmentxenografts

Identifiers

PMID38450798
PMCPMC11014775

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Registered trials

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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.