Evidence map›Paper›PMID 30656716›Full record

ArticleThe Prostate2019

PSMA expression in the Hi-Myc model; extended utility of a representative model of prostate adenocarcinoma for biological insight and as a drug discovery tool.

Brian W Simons, Norman F Turtle, David H Ulmert, Diane S Abou, Daniel L J Thorek

Open access · hybridAbstract read
In one paragraph

Article in The Prostate, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Receptor-Targeted Peptide Conjugates Based on Diphosphines Enable Preparation ofJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2024
    Article
  12. Article
  13. Article
  14. GCP III is not the "off-target" for urea-based PSMA ligands.European journal of nuclear medicine and molecular imaging · 2023
    Article
  15. Review
  16. Review
  17. 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

5 authors at 3 institutions in 1 country.

Brian W SimonsCenter for Comparative Medicine, Baylor College of Medicine, Houston, Texas.
Norman F TurtleRadiological Chemistry Imaging Laboratory, Mallinckrodt Institute of Radiology, Washington University in St. Louis, St. Louis, Missouri.
David H UlmertJohnsson Comprehensive Cancer Center, University of California, Los Angeles, California.
Diane S AbouRadiological Chemistry Imaging Laboratory, Mallinckrodt Institute of Radiology, Washington University in St. Louis, St. Louis, Missouri.
Daniel L J ThorekRadiological Chemistry Imaging Laboratory, Mallinckrodt Institute of Radiology, Washington University in St. Louis, St. Louis, Missouri.ORCID 0000-0003-2437-1239
Washington University in St. Louis · USBaylor College of Medicine · USUniversity of California, Los Angeles · US

Funding

Opening the Therapeutic Window for PSMA-Targeted Molecular RadiotherapyR01CA229893 · NCI · WASHINGTON UNIVERSITY · PI THOREK, DANIEL LYNDON JAFFE · 2019 to 2024
$1.9M
Kallikrein-Targeted Alpha-Particle Therapy of Late-Stage Prostate CancerR01CA201035 · NCI · WASHINGTON UNIVERSITY · PI THOREK, DANIEL LYNDON JAFFE · 2017 to 2020
$1.4M
NCI NIH HHS R01 CA201035NCI NIH HHS R01 CA229893NCI NIH HHS R01CA229893NIH HHS R01 CA201035
6 · The paper itself

Abstract

Prostate-specific membrane antigen (PSMA), also known as glutamate carboxypeptidase II (GCPII), is highly overexpressed in primary and metastatic prostate cancer (PCa). This has led to the development of radiopharmaceuticals for targeted imaging and therapy under current clinical evaluation. Despite this progress, the exact biological role of the protein in prostate cancer development and progression has not been fully elucidated. This is in part because the human PSMA and mouse PSMA (mPSMA) have different patterns of anatomical expression which confound study in the most widely utilized model organisms. Most notably, mPSMA is not expressed in the healthy murine prostate. Here, we reveal that mPSMA is highly upregulated in the prostate adenocarcinoma of the spontaneous Hi-Myc mouse model, a highly accurate and well characterized mouse model of prostate cancer development. Antibody detection and molecular imaging tools are used to confirm that mPSMA is expressed from early prostatic intraepithelial neoplasia (PIN) through adenocarcinoma.

Indexed as

AdenocarcinomaProstateProstatic NeoplasmsAnimalsAntigens, SurfaceDisease Models, AnimalDrug DiscoveryGene Expression Regulation, NeoplasticGlutamate Carboxypeptidase IIHumansImmunohistochemistryMaleMembrane GlycoproteinsMiceMolecular ImagingMolecular Targeted TherapyAntigens, SurfaceFOLH1 protein, humanGlutamate Carboxypeptidase IIMembrane GlycoproteinsPSMA protein, mouseRadiopharmaceuticalsdrug developmentmouse modelsprostate cancerPSMA

Identifiers

PMID30656716
PMCPMC6519119
OpenAlexW2951371072

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.