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

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 urin...

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Autores principales: Neveu, Bertrand, Jain, Pallavi, Têtu, Bernard, Wu, Lily, Fradet, Yves, Pouliot, Frédéric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811461/
https://www.ncbi.nlm.nih.gov/pubmed/26594800
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author Neveu, Bertrand
Jain, Pallavi
Têtu, Bernard
Wu, Lily
Fradet, Yves
Pouliot, Frédéric
author_facet Neveu, Bertrand
Jain, Pallavi
Têtu, Bernard
Wu, Lily
Fradet, Yves
Pouliot, Frédéric
author_sort Neveu, Bertrand
collection PubMed
description 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.
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spelling pubmed-48114612016-04-25 A PCA3 gene-based transcriptional amplification system targeting primary prostate cancer Neveu, Bertrand Jain, Pallavi Têtu, Bernard Wu, Lily Fradet, Yves Pouliot, Frédéric Oncotarget Research Paper 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. Impact Journals LLC 2015-11-22 /pmc/articles/PMC4811461/ /pubmed/26594800 Text en Copyright: © 2016 Neveu et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Neveu, Bertrand
Jain, Pallavi
Têtu, Bernard
Wu, Lily
Fradet, Yves
Pouliot, Frédéric
A PCA3 gene-based transcriptional amplification system targeting primary prostate cancer
title A PCA3 gene-based transcriptional amplification system targeting primary prostate cancer
title_full A PCA3 gene-based transcriptional amplification system targeting primary prostate cancer
title_fullStr A PCA3 gene-based transcriptional amplification system targeting primary prostate cancer
title_full_unstemmed A PCA3 gene-based transcriptional amplification system targeting primary prostate cancer
title_short A PCA3 gene-based transcriptional amplification system targeting primary prostate cancer
title_sort pca3 gene-based transcriptional amplification system targeting primary prostate cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811461/
https://www.ncbi.nlm.nih.gov/pubmed/26594800
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