Evidence map›Paper›PMID 30467556›Full record

ArticleEuropean urology oncology2018

Patient-derived Models Reveal Impact of the Tumor Microenvironment on Therapeutic Response.

Ayesha A Shafi, Matthew J Schiewer, Renée de Leeuw, Emanuela Dylgjeri, Peter A McCue, Neelima Shah, Leonard G Gomella, Costas D Lallas, Edouard J Trabulsi, Margaret M Centenera and 6 more

Abstract read
In one paragraph

Article in European urology oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 9% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Making In Vitro Tumor Models Whole Again.Advanced healthcare materials · 2023
    Review
  12. Review
  13. Review
  14. Prevalence of tumour-infiltrating CD103British journal of cancer · 2023
    Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. A Novel Role for DNA-PK in Metabolism by Regulating Glycolysis in Castration-Resistant Prostate Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    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

16 authors at 6 institutions in 2 countries.

Ayesha A ShafiSidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.
Matthew J SchiewerSidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.
Renée de LeeuwSidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.
Emanuela DylgjeriSidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.
Peter A McCueSidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.
Neelima ShahCancer Biology, Fox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Leonard G GomellaSidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.
Costas D LallasSidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.
Edouard J TrabulsiSidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.
Margaret M CenteneraDame Roma Mitchell Cancer Research Laboratories, Adelaide Prostate Cancer Research Centre and Freemason's Foundation Centre for Men's Health, School of Medicine, University of Adelaide, Adelaide, Australia.
Theresa E HickeyDame Roma Mitchell Cancer Research Laboratories, Adelaide Prostate Cancer Research Centre and Freemason's Foundation Centre for Men's Health, School of Medicine, University of Adelaide, Adelaide, Australia.
Lisa M ButlerDame Roma Mitchell Cancer Research Laboratories, Adelaide Prostate Cancer Research Centre and Freemason's Foundation Centre for Men's Health, School of Medicine, University of Adelaide, Adelaide, Australia.
Ganesh RajUniversity of Texas Southwestern Medical Center, Dallas, TX, USA.
Wayne D TilleyDame Roma Mitchell Cancer Research Laboratories, Adelaide Prostate Cancer Research Centre and Freemason's Foundation Centre for Men's Health, School of Medicine, University of Adelaide, Adelaide, Australia.
Edna CukiermanCancer Biology, Fox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Karen E KnudsenSidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA, USA.
Sidney Kimmel Cancer Center · USThomas Jefferson University · USUniversity of Adelaide · AUFox Chase Cancer Center · USSouth Australian Health and Medical Research Institute · AUThe University of Texas Southwestern Medical Center · US

Funding

WORD PROCESSING CENTER--COREP30CA006927 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI Dietmar J Kappes · 1985 to 2026
$138.8M
X-Ray Crystallography and Macromolecular CharacterizationP30CA056036 · NCI · THOMAS JEFFERSON UNIVERSITY · PI Andrew Chapman · 1995 to 2026
$94.8M
3D-Adhesion Stromagenesis in Cancer PermissivenessR01CA113451 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI CUKIERMAN, EDNA · 2006 to 2016
$2.8M
USP22 Function in Advanced Prostate CancerR01CA182569 · NCI · THOMAS JEFFERSON UNIVERSITY · PI KNUDSEN, KAREN E, MCMAHON, STEVEN B. · 2015 to 2019
$2.4M
RB Function in Prostate Cancer ProgressionR01CA176401 · NCI · THOMAS JEFFERSON UNIVERSITY · PI KNUDSEN, KAREN E · 2014 to 2018
$2.2M
Targeting Cell Cycle Alterations to Improve Treatment for Advanced Prostate CancerR01CA217329 · NCI · THOMAS JEFFERSON UNIVERSITY · PI KELLY, WILLIAM K., MCNAIR, CHRISTOPHER MICHAEL · 2017 to 2021
$1.8M
SWI/SNF dysregulation in development and diseaseR01CA159945 · NCI · THOMAS JEFFERSON UNIVERSITY · PI KNUDSEN, KAREN E · 2012 to 2016
$1.6M
NCI NIH HHS P30 CA006927NCI NIH HHS P30 CA056036NCI NIH HHS R01 CA113451NCI NIH HHS R01 CA159945NCI NIH HHS R01 CA176401NCI NIH HHS R01 CA182569NCI NIH HHS R01 CA217329
6 · The paper itself

Abstract

backgroundAndrogen deprivation therapy is a first-line treatment for disseminated prostate cancer (PCa). However, virtually all tumors become resistant and recur as castration-resistant PCa, which has no durable cure. One major hurdle in the development of more effective therapies is the lack of preclinical models that adequately recapitulate the heterogeneity of PCa, significantly hindering the ability to accurately predict therapeutic response.

objectiveTo leverage the ex vivo culture method termed DESIGN SETTING AND

participantsFresh PCa tissue from patients who underwent radical prostatectomy was cultured as PDEs to examine therapeutic response. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: The impact of genomic and chemical perturbations in PDEs was assessed using various parameters (eg, AR levels, Ki67 staining, and desmoplastic indices). RESULTS AND LIMITATIONS: PDE maintained the integrity of the native tumor microenvironment (TME), tumor tissue morphology, viability, and endogenous hormone signaling. Tumor cells in this model system exhibited de novo proliferative capacity. Examination of the native TME in the PDE revealed a first-in-field insight into patient-specific desmoplastic stromal indices and predicted responsiveness to AR-directed therapeutics.

conclusionsThe PDE model allows for a comprehensive evaluation of individual tumors in their native TME to ultimately develop more effective therapeutic regimens tailored to individuals. Discernment of novel stromal markers may provide a basis for applying precision medicine in treating advanced PCa, which would have a transformative effect on patient outcomes. PATIENT SUMMARY: In this study, an innovative model system was used to more effectively mimic human disease. The patient-derived explant (PDE) system can be used to predict therapeutic response and identify novel targets in advanced disease. Thus, the PDE will be an asset for the development of novel metrics for the implementation of precision medicine in prostate cancer.The patient-derived explant (PDE) model allows for a comprehensive evaluation of individual human tumors in their native tumor microenvironment (TME). TME analysis revealed first-in-field insight into predicted tumor responsiveness to AR-directed therapeutics through evaluation of patient-specific desmoplastic stromal indices.

Indexed as

Androgen receptorEx vivoProstate cancerTumor microenvironment

Identifiers

PMID30467556
PMCPMC6241309
OpenAlexW2807581044

What OpenQuestion holds

Textmetadata
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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.