Evidence map›Paper›PMID 35406480›Full record

ArticleCancers2022

Harnessing the Heterogeneity of Prostate Cancer for Target Discovery Using Patient-Derived Explants.

Margaret M Centenera, Andrew D Vincent, Max Moldovan, Hui-Ming Lin, David J Lynn, Lisa G Horvath, Lisa M Butler

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. 3D Culture Analysis of Cancer Cell Adherence toTissue engineering. Part C, Methods · 2024
    Article
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  7. Review
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  11. Making In Vitro Tumor Models Whole Again.Advanced healthcare materials · 2023
    Review
  12. 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

7 authors at 6 institutions in 1 country.

Margaret M CenteneraAdelaide Medical School, University of Adelaide, North Terrace, Adelaide, SA 5000, Australia.ORCID 0000-0002-2206-0632
Andrew D VincentAdelaide Medical School, University of Adelaide, North Terrace, Adelaide, SA 5000, Australia.
Max MoldovanBiometry Hub, Faculty of Science, University of Adelaide, Waite Campus, SA 5005, Australia.
Hui-Ming LinGarvan Institute for Medical Research, Darlinghurst, NSW 2010, Australia.ORCID 0000-0003-4892-6008
David J LynnPrecision Medicine Theme, South Australian Health and Medical Research Institute, North Terrace, Adelaide, SA 5000, Australia.ORCID 0000-0003-4664-1404
Lisa G HorvathGarvan Institute for Medical Research, Darlinghurst, NSW 2010, Australia.
Lisa M ButlerAdelaide Medical School, University of Adelaide, North Terrace, Adelaide, SA 5000, Australia.ORCID 0000-0003-2698-3220
South Australian Health and Medical Research Institute · AUFlinders University · AUFreemasons Foundation Centre for Men's Health · AUGarvan Institute of Medical Research · AUThe University of Adelaide · AUThe University of Sydney · AU

Funding

Beat Cancer SA PRF1117Cancer Australia 1085471Cancer Institute of New South Wales TPG172146Freemasons Foundation Centre for Men's Health FellowshipHospital Research Foundation C-PJ-03-Prost-2020Movember Foundation MRTA3National Health and Medical Research Council 1196225
6 · The paper itself

Abstract

Prostate cancer is a complex and heterogeneous disease, but a small number of cell lines have dominated basic prostate cancer research, representing a major obstacle in the field of drug and biomarker discovery. A growing lack of confidence in cell lines has seen a shift toward more sophisticated pre-clinical cancer models that incorporate patient-derived tumors as xenografts or explants, to more accurately reflect clinical disease. Not only do these models retain critical features of the original tumor, and account for the molecular diversity and cellular heterogeneity of prostate cancer, but they provide a unique opportunity to conduct research in matched tumor samples. The challenge that accompanies these complex tissue models is increased complexity of analysis. With over 10 years of experience working with patient-derived explants (PDEs) of prostate cancer, this study provides guidance on the PDE method, its limitations, and considerations for addressing the heterogeneity of prostate cancer PDEs that are based on statistical modeling. Using inhibitors of the molecular chaperone heat shock protein 90 (Hsp90) as an example of a drug that induces robust proliferative response, we demonstrate how multi-omics analysis in prostate cancer PDEs is both feasible and essential for identification of key biological pathways, with significant potential for novel drug target and biomarker discovery.

Indexed as

patient-derived explantpre-clinical tumor modelprostate cancerproteomicstranscriptomics

Identifiers

PMID35406480
PMCPMC8996971
OpenAlexW4220914251

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.