Evidence map›Paper›PMID 26594800›Full record

ArticleOncotarget2016

A PCA3 gene-based transcriptional amplification system targeting primary prostate cancer.

Bertrand Neveu, Pallavi Jain, Bernard Têtu, Lily Wu, Yves Fradet, Frédéric Pouliot

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Sex steroid modulation of macrophages within the prostate tumor microenvironment.American journal of clinical and experimental urology · 2022
    Article
  5. Article
  6. Observational
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Long Non-Coding RNA as Potential Biomarker for Prostate Cancer: Is It Making a Difference?International journal of environmental research and public health · 2017
    Review
  13. Article
  14. Article
  15. 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

6 authors at 3 institutions in 2 countries.

Bertrand NeveuDépartement de Chirurgie, Faculté de Médecine, Université Laval, Centre de Recherche du Centre Hospitalier Universitaire de Québec, Québec, Canada.
Pallavi JainDépartement de Chirurgie, Faculté de Médecine, Université Laval, Centre de Recherche du Centre Hospitalier Universitaire de Québec, Québec, Canada.
Bernard TêtuDépartement de Biochimie et Pathologie, Faculté de Médecine, Université Laval, Centre Hospitalier Universitaire de Québec, Québec, Canada.
Lily WuDepartment of Molecular and Medical Pharmacology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA.
Yves FradetDépartement de Chirurgie, Faculté de Médecine, Université Laval, Centre de Recherche du Centre Hospitalier Universitaire de Québec, Québec, Canada.
Frédéric PouliotDépartement de Chirurgie, Faculté de Médecine, Université Laval, Centre de Recherche du Centre Hospitalier Universitaire de Québec, Québec, Canada.
Centre hospitalier universitaire de Québec · CAUniversité Laval · CAUniversity of California, Los Angeles · US

Funding

UCLA SPORE IN PROSTATE CANCERP50CA092131 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI FREEMAN, MICHAEL R · 2002 to 2023
$42.6M
NCI NIH HHS P50 CA092131
6 · The paper itself

Abstract

Targeting specifically primary prostate cancer (PCa) cells for immune therapy, gene therapy or molecular imaging is of high importance. The PCA3 long non-coding RNA is a unique PCa biomarker and oncogene that has been widely studied. This gene has been mainly exploited as an accurate diagnostic urine biomarker for PCa detection. In this study, the PCA3 promoter was introduced into a new transcriptional amplification system named the 3-Step Transcriptional Amplification System (PCA3-3STA) and cloned into type 5 adenovirus. PCA3-3STA activity was highly specific for PCa cells, ranging between 98.7- and 108.0-fold higher than that for benign primary prostate epithelial or non-PCa cells, respectively. In human PCa xenografts, PCA3-3STA displayed robust bioluminescent signals at levels that are sufficient to translate to positron emission tomography (PET)-based reporter imaging. Remarkably, when freshly isolated benign or cancerous prostate biopsies were infected with PCA3-3STA, the optical signal produced from primary PCa biopsies was significantly higher than from benign prostate biopsies (4.4-fold, p < 0.0001). PCA3-3STA therefore represents a PCa-specific expression system with the potential to target, with high accuracy, primary or metastatic PCa epithelial cells for imaging, vaccines, or gene therapy.

Indexed as

Gene AmplificationTranscriptional ActivationAgedAged, 80 and overAndrogensAnimalsAntigens, NeoplasmCell LineCell Line, TumorDihydrotestosteroneGene Expression Regulation, NeoplasticHep G2 CellsHumansMaleMice, SCIDMiddle AgedAndrogensAntigens, NeoplasmDihydrotestosteroneprostate cancer antigen 3, humannon-invasive imaging in animalPCA3prostate cancervector system and targeting strategies

Identifiers

PMID26594800
PMCPMC4811461
OpenAlexW2172507926

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.