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Increased Plasmatic Levels of PSA-Expressing Exosomes Distinguish Prostate Cancer Patients from Benign Prostatic Hyperplasia: A Prospective Study

Prostate Specific Antigen (PSA) fails to discriminate between benign prostatic hyperplasia (BPH) and Prostate Cancer (PCa), resulting in large numbers of unnecessary biopsies and missed cancer diagnoses. Nanovesicles called exosomes are directly detectable in patient plasma and here we explore the p...

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Autores principales: Logozzi, Mariantonia, Angelini, Daniela F., Giuliani, Alessandro, Mizzoni, Davide, Di Raimo, Rossella, Maggi, Martina, Gentilucci, Alessandro, Marzio, Vittorio, Salciccia, Stefano, Borsellino, Giovanna, Battistini, Luca, Sciarra, Alessandro, Fais, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826376/
https://www.ncbi.nlm.nih.gov/pubmed/31569672
http://dx.doi.org/10.3390/cancers11101449
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author Logozzi, Mariantonia
Angelini, Daniela F.
Giuliani, Alessandro
Mizzoni, Davide
Di Raimo, Rossella
Maggi, Martina
Gentilucci, Alessandro
Marzio, Vittorio
Salciccia, Stefano
Borsellino, Giovanna
Battistini, Luca
Sciarra, Alessandro
Fais, Stefano
author_facet Logozzi, Mariantonia
Angelini, Daniela F.
Giuliani, Alessandro
Mizzoni, Davide
Di Raimo, Rossella
Maggi, Martina
Gentilucci, Alessandro
Marzio, Vittorio
Salciccia, Stefano
Borsellino, Giovanna
Battistini, Luca
Sciarra, Alessandro
Fais, Stefano
author_sort Logozzi, Mariantonia
collection PubMed
description Prostate Specific Antigen (PSA) fails to discriminate between benign prostatic hyperplasia (BPH) and Prostate Cancer (PCa), resulting in large numbers of unnecessary biopsies and missed cancer diagnoses. Nanovesicles called exosomes are directly detectable in patient plasma and here we explore the potential use of plasmatic exosomes expressing PSA (Exo-PSA) in distinguishing healthy individuals, BPH, and PCa. Exosomes were obtained from plasma samples of 80 PCa, 80 BPH, and 80 healthy donors (CTR). Nanoparticle Tracking Analysis (NTA), immunocapture-based ELISA (IC-ELISA), and nanoscale flow-cytometry (NSFC), were exploited to detect and characterize plasmatic exosomes. Statistical analysis showed that plasmatic exosomes expressing both CD81 and PSA were significantly higher in PCa as compared to both BPH and CTR, reaching 100% specificity and sensitivity in distinguishing PCa patients from healthy individuals. IC-ELISA, NSFC, and Exo-PSA consensus score (EXOMIX) showed 98% to 100% specificity and sensitivity for BPH-PCa discrimination. This study outperforms the conventional PSA test with a minimally invasive widely exploitable approach.
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spelling pubmed-68263762019-11-18 Increased Plasmatic Levels of PSA-Expressing Exosomes Distinguish Prostate Cancer Patients from Benign Prostatic Hyperplasia: A Prospective Study Logozzi, Mariantonia Angelini, Daniela F. Giuliani, Alessandro Mizzoni, Davide Di Raimo, Rossella Maggi, Martina Gentilucci, Alessandro Marzio, Vittorio Salciccia, Stefano Borsellino, Giovanna Battistini, Luca Sciarra, Alessandro Fais, Stefano Cancers (Basel) Article Prostate Specific Antigen (PSA) fails to discriminate between benign prostatic hyperplasia (BPH) and Prostate Cancer (PCa), resulting in large numbers of unnecessary biopsies and missed cancer diagnoses. Nanovesicles called exosomes are directly detectable in patient plasma and here we explore the potential use of plasmatic exosomes expressing PSA (Exo-PSA) in distinguishing healthy individuals, BPH, and PCa. Exosomes were obtained from plasma samples of 80 PCa, 80 BPH, and 80 healthy donors (CTR). Nanoparticle Tracking Analysis (NTA), immunocapture-based ELISA (IC-ELISA), and nanoscale flow-cytometry (NSFC), were exploited to detect and characterize plasmatic exosomes. Statistical analysis showed that plasmatic exosomes expressing both CD81 and PSA were significantly higher in PCa as compared to both BPH and CTR, reaching 100% specificity and sensitivity in distinguishing PCa patients from healthy individuals. IC-ELISA, NSFC, and Exo-PSA consensus score (EXOMIX) showed 98% to 100% specificity and sensitivity for BPH-PCa discrimination. This study outperforms the conventional PSA test with a minimally invasive widely exploitable approach. MDPI 2019-09-27 /pmc/articles/PMC6826376/ /pubmed/31569672 http://dx.doi.org/10.3390/cancers11101449 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Logozzi, Mariantonia
Angelini, Daniela F.
Giuliani, Alessandro
Mizzoni, Davide
Di Raimo, Rossella
Maggi, Martina
Gentilucci, Alessandro
Marzio, Vittorio
Salciccia, Stefano
Borsellino, Giovanna
Battistini, Luca
Sciarra, Alessandro
Fais, Stefano
Increased Plasmatic Levels of PSA-Expressing Exosomes Distinguish Prostate Cancer Patients from Benign Prostatic Hyperplasia: A Prospective Study
title Increased Plasmatic Levels of PSA-Expressing Exosomes Distinguish Prostate Cancer Patients from Benign Prostatic Hyperplasia: A Prospective Study
title_full Increased Plasmatic Levels of PSA-Expressing Exosomes Distinguish Prostate Cancer Patients from Benign Prostatic Hyperplasia: A Prospective Study
title_fullStr Increased Plasmatic Levels of PSA-Expressing Exosomes Distinguish Prostate Cancer Patients from Benign Prostatic Hyperplasia: A Prospective Study
title_full_unstemmed Increased Plasmatic Levels of PSA-Expressing Exosomes Distinguish Prostate Cancer Patients from Benign Prostatic Hyperplasia: A Prospective Study
title_short Increased Plasmatic Levels of PSA-Expressing Exosomes Distinguish Prostate Cancer Patients from Benign Prostatic Hyperplasia: A Prospective Study
title_sort increased plasmatic levels of psa-expressing exosomes distinguish prostate cancer patients from benign prostatic hyperplasia: a prospective study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826376/
https://www.ncbi.nlm.nih.gov/pubmed/31569672
http://dx.doi.org/10.3390/cancers11101449
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