Increased PSA expression on prostate cancer exosomes in in vitro condition and in cancer patients

Prostate specific antigen (PSA) test is the most common, clinically validated test for the diagnosis of prostate cancer (PCa). While neoplastic lesions of the prostate may cause aberrant levels of PSA in the blood, the quantitation of free or complexed PSA poorly discriminates cancer patients from t...

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Published inCancer letters Vol. 403; pp. 318 - 329
Main Authors Logozzi, Mariantonia, Angelini, Daniela F., Iessi, Elisabetta, Mizzoni, Davide, Di Raimo, Rossella, Federici, Cristina, Lugini, Luana, Borsellino, Giovanna, Gentilucci, Alessandro, Pierella, Federico, Marzio, Vittorio, Sciarra, Alessandro, Battistini, Luca, Fais, Stefano
Format Journal Article
LanguageEnglish
Published Ireland Elsevier B.V 10.09.2017
Elsevier Limited
Subjects
Online AccessGet full text
ISSN0304-3835
1872-7980
1872-7980
DOI10.1016/j.canlet.2017.06.036

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Abstract Prostate specific antigen (PSA) test is the most common, clinically validated test for the diagnosis of prostate cancer (PCa). While neoplastic lesions of the prostate may cause aberrant levels of PSA in the blood, the quantitation of free or complexed PSA poorly discriminates cancer patients from those developing benign lesions, often leading to invasive and unnecessary surgical procedures. Microenvironmental acidity increases exosome release by cancer cells. In this study we evaluated whether acidity, a critical phenotype of malignancy, could influence exosome release and increase the PSA expression in nanovesicles released by PCa cells. To this aim, we exploited Nanoparticle Tracking Analysis (NTA), an immunocapture-based ELISA, and nanoscale flow-cytometry. The results show that microenvironmental acidity induces an increased release of nanovesicles expressing both PSA and the exosome marker CD81. In order to verify whether the changes induced by the local selective pressure of extracellular acidity may correspond to a clinical pathway we used the same approach to evaluate the levels of PSA-expressing exosomes in the plasma of PCa patients and controls, including subjects with benign prostatic hypertrophy (BPH). The results show that only PCa patients have high levels of nanovesicles expressing both CD81 and PSA. This study shows that tumor acidity exerts a selective pressure leading to the release of extracellular vesicles that express both PSA and exosome markers. A comparable scenario was shown in the plasma of prostate cancer patients as compared to both BPH and healthy controls. These results suggest that microenvironmental acidity may represent a key factor which determines qualitatively and quantitatively the release of extracellular vesicles by malignant tumors, including prostate cancer. This condition leads to the spill-over of nanovesicles into the peripheral blood of prostate cancer patients, where the levels of tumor biomarkers expressed by exosomes, such as PSA-exosomes, may represent a novel, non-invasive clinical tool for the screening and early diagnosis of prostate cancer. •PSA prostate-specific antigen (PSA) is a prostate cancer (PCa) specific marker.•Microenvironmental acidity increases exosome release by cancer cells.•Acidity induces expression of PSA by exosomes.•PCa patients had high levels of PSA-expressing exosomes.•Tumor acidity exerts a selective pressure leading to expression of PSA by exosomes, leading in turn to the spilling over of PSA-expressing exosomes in the blood of PCa patients.•The use of plasmatic PSA-exosomes may be a novel, non-invasive clinical tool for screening and early diagnosis of prostate cancer.
AbstractList Prostate specific antigen (PSA) test is the most common, clinically validated test for the diagnosis of prostate cancer (PCa). While neoplastic lesions of the prostate may cause aberrant levels of PSA in the blood, the quantitation of free or complexed PSA poorly discriminates cancer patients from those developing benign lesions, often leading to invasive and unnecessary surgical procedures. Microenvironmental acidity increases exosome release by cancer cells. In this study we evaluated whether acidity, a critical phenotype of malignancy, could influence exosome release and increase the PSA expression in nanovesicles released by PCa cells. To this aim, we exploited Nanoparticle Tracking Analysis (NTA), an immunocapture-based ELISA, and nanoscale flow-cytometry. The results show that microenvironmental acidity induces an increased release of nanovesicles expressing both PSA and the exosome marker CD81. In order to verify whether the changes induced by the local selective pressure of extracellular acidity may correspond to a clinical pathway we used the same approach to evaluate the levels of PSA-expressing exosomes in the plasma of PCa patients and controls, including subjects with benign prostatic hypertrophy (BPH). The results show that only PCa patients have high levels of nanovesicles expressing both CD81 and PSA. This study shows that tumor acidity exerts a selective pressure leading to the release of extracellular vesicles that express both PSA and exosome markers. A comparable scenario was shown in the plasma of prostate cancer patients as compared to both BPH and healthy controls. These results suggest that microenvironmental acidity may represent a key factor which determines qualitatively and quantitatively the release of extracellular vesicles by malignant tumors, including prostate cancer. This condition leads to the spill-over of nanovesicles into the peripheral blood of prostate cancer patients, where the levels of tumor biomarkers expressed by exosomes, such as PSA-exosomes, may represent a novel, non-invasive clinical tool for the screening and early diagnosis of prostate cancer.Prostate specific antigen (PSA) test is the most common, clinically validated test for the diagnosis of prostate cancer (PCa). While neoplastic lesions of the prostate may cause aberrant levels of PSA in the blood, the quantitation of free or complexed PSA poorly discriminates cancer patients from those developing benign lesions, often leading to invasive and unnecessary surgical procedures. Microenvironmental acidity increases exosome release by cancer cells. In this study we evaluated whether acidity, a critical phenotype of malignancy, could influence exosome release and increase the PSA expression in nanovesicles released by PCa cells. To this aim, we exploited Nanoparticle Tracking Analysis (NTA), an immunocapture-based ELISA, and nanoscale flow-cytometry. The results show that microenvironmental acidity induces an increased release of nanovesicles expressing both PSA and the exosome marker CD81. In order to verify whether the changes induced by the local selective pressure of extracellular acidity may correspond to a clinical pathway we used the same approach to evaluate the levels of PSA-expressing exosomes in the plasma of PCa patients and controls, including subjects with benign prostatic hypertrophy (BPH). The results show that only PCa patients have high levels of nanovesicles expressing both CD81 and PSA. This study shows that tumor acidity exerts a selective pressure leading to the release of extracellular vesicles that express both PSA and exosome markers. A comparable scenario was shown in the plasma of prostate cancer patients as compared to both BPH and healthy controls. These results suggest that microenvironmental acidity may represent a key factor which determines qualitatively and quantitatively the release of extracellular vesicles by malignant tumors, including prostate cancer. This condition leads to the spill-over of nanovesicles into the peripheral blood of prostate cancer patients, where the levels of tumor biomarkers expressed by exosomes, such as PSA-exosomes, may represent a novel, non-invasive clinical tool for the screening and early diagnosis of prostate cancer.
Prostate specific antigen (PSA) test is the most common, clinically validated test for the diagnosis of prostate cancer (PCa). While neoplastic lesions of the prostate may cause aberrant levels of PSA in the blood, the quantitation of free or complexed PSA poorly discriminates cancer patients from those developing benign lesions, often leading to invasive and unnecessary surgical procedures. Microenvironmental acidity increases exosome release by cancer cells. In this study we evaluated whether acidity, a critical phenotype of malignancy, could influence exosome release and increase the PSA expression in nanovesicles released by PCa cells. To this aim, we exploited Nanoparticle Tracking Analysis (NTA), an immunocapture-based ELISA, and nanoscale flow-cytometry. The results show that microenvironmental acidity induces an increased release of nanovesicles expressing both PSA and the exosome marker CD81. In order to verify whether the changes induced by the local selective pressure of extracellular acidity may correspond to a clinical pathway we used the same approach to evaluate the levels of PSA-expressing exosomes in the plasma of PCa patients and controls, including subjects with benign prostatic hypertrophy (BPH). The results show that only PCa patients have high levels of nanovesicles expressing both CD81 and PSA. This study shows that tumor acidity exerts a selective pressure leading to the release of extracellular vesicles that express both PSA and exosome markers. A comparable scenario was shown in the plasma of prostate cancer patients as compared to both BPH and healthy controls. These results suggest that microenvironmental acidity may represent a key factor which determines qualitatively and quantitatively the release of extracellular vesicles by malignant tumors, including prostate cancer. This condition leads to the spill-over of nanovesicles into the peripheral blood of prostate cancer patients, where the levels of tumor biomarkers expressed by exosomes, such as PSA-exosomes, may represent a novel, non-invasive clinical tool for the screening and early diagnosis of prostate cancer. •PSA prostate-specific antigen (PSA) is a prostate cancer (PCa) specific marker.•Microenvironmental acidity increases exosome release by cancer cells.•Acidity induces expression of PSA by exosomes.•PCa patients had high levels of PSA-expressing exosomes.•Tumor acidity exerts a selective pressure leading to expression of PSA by exosomes, leading in turn to the spilling over of PSA-expressing exosomes in the blood of PCa patients.•The use of plasmatic PSA-exosomes may be a novel, non-invasive clinical tool for screening and early diagnosis of prostate cancer.
Prostate specific antigen (PSA) test is the most common, clinically validated test for the diagnosis of prostate cancer (PCa). While neoplastic lesions of the prostate may cause aberrant levels of PSA in the blood, the quantitation of free or complexed PSA poorly discriminates cancer patients from those developing benign lesions, often leading to invasive and unnecessary surgical procedures. Microenvironmental acidity increases exosome release by cancer cells. In this study we evaluated whether acidity, a critical phenotype of malignancy, could influence exosome release and increase the PSA expression in nanovesicles released by PCa cells. To this aim, we exploited Nanoparticle Tracking Analysis (NTA), an immunocapture-based ELISA, and nanoscale flow-cytometry. The results show that microenvironmental acidity induces an increased release of nanovesicles expressing both PSA and the exosome marker CD81. In order to verify whether the changes induced by the local selective pressure of extracellular acidity may correspond to a clinical pathway we used the same approach to evaluate the levels of PSA-expressing exosomes in the plasma of PCa patients and controls, including subjects with benign prostatic hypertrophy (BPH). The results show that only PCa patients have high levels of nanovesicles expressing both CD81 and PSA. This study shows that tumor acidity exerts a selective pressure leading to the release of extracellular vesicles that express both PSA and exosome markers. A comparable scenario was shown in the plasma of prostate cancer patients as compared to both BPH and healthy controls. These results suggest that microenvironmental acidity may represent a key factor which determines qualitatively and quantitatively the release of extracellular vesicles by malignant tumors, including prostate cancer. This condition leads to the spill-over of nanovesicles into the peripheral blood of prostate cancer patients, where the levels of tumor biomarkers expressed by exosomes, such as PSA-exosomes, may represent a novel, non-invasive clinical tool for the screening and early diagnosis of prostate cancer.
Author Sciarra, Alessandro
Logozzi, Mariantonia
Di Raimo, Rossella
Fais, Stefano
Gentilucci, Alessandro
Battistini, Luca
Angelini, Daniela F.
Marzio, Vittorio
Iessi, Elisabetta
Pierella, Federico
Federici, Cristina
Lugini, Luana
Mizzoni, Davide
Borsellino, Giovanna
Author_xml – sequence: 1
  givenname: Mariantonia
  surname: Logozzi
  fullname: Logozzi, Mariantonia
  organization: Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy
– sequence: 2
  givenname: Daniela F.
  surname: Angelini
  fullname: Angelini, Daniela F.
  organization: Neuroimmunology Unit, IRCCS Santa Lucia Foundation, 00179 Rome, Italy
– sequence: 3
  givenname: Elisabetta
  surname: Iessi
  fullname: Iessi, Elisabetta
  organization: Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy
– sequence: 4
  givenname: Davide
  surname: Mizzoni
  fullname: Mizzoni, Davide
  organization: Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy
– sequence: 5
  givenname: Rossella
  surname: Di Raimo
  fullname: Di Raimo, Rossella
  organization: Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy
– sequence: 6
  givenname: Cristina
  surname: Federici
  fullname: Federici, Cristina
  organization: Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy
– sequence: 7
  givenname: Luana
  surname: Lugini
  fullname: Lugini, Luana
  organization: Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy
– sequence: 8
  givenname: Giovanna
  surname: Borsellino
  fullname: Borsellino, Giovanna
  organization: Neuroimmunology Unit, IRCCS Santa Lucia Foundation, 00179 Rome, Italy
– sequence: 9
  givenname: Alessandro
  surname: Gentilucci
  fullname: Gentilucci, Alessandro
  organization: Department of Urological Sciences, Policlinico Umberto I, University Sapienza, Rome, Italy
– sequence: 10
  givenname: Federico
  surname: Pierella
  fullname: Pierella, Federico
  organization: Department of Urological Sciences, Policlinico Umberto I, University Sapienza, Rome, Italy
– sequence: 11
  givenname: Vittorio
  surname: Marzio
  fullname: Marzio, Vittorio
  organization: Department of Urological Sciences, Policlinico Umberto I, University Sapienza, Rome, Italy
– sequence: 12
  givenname: Alessandro
  surname: Sciarra
  fullname: Sciarra, Alessandro
  organization: Department of Urological Sciences, Policlinico Umberto I, University Sapienza, Rome, Italy
– sequence: 13
  givenname: Luca
  surname: Battistini
  fullname: Battistini, Luca
  organization: Neuroimmunology Unit, IRCCS Santa Lucia Foundation, 00179 Rome, Italy
– sequence: 14
  givenname: Stefano
  orcidid: 0000-0001-9060-2766
  surname: Fais
  fullname: Fais, Stefano
  email: stefano.fais@iss.it
  organization: Department of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Viale Regina Elena 299, 00161 Rome, Italy
BackLink https://www.ncbi.nlm.nih.gov/pubmed/28694142$$D View this record in MEDLINE/PubMed
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Snippet Prostate specific antigen (PSA) test is the most common, clinically validated test for the diagnosis of prostate cancer (PCa). While neoplastic lesions of the...
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SubjectTerms Acidification
Acidity
Antibiotics
Antigens
Benign
Biomarkers
Biopsy
Cancer
Case-Control Studies
CD81 antigen
Cell culture
Cell Line, Tumor
Cytometry
Early Detection of Cancer
ELISA
Enzyme-Linked Immunosorbent Assay
Exosomes
Exosomes - metabolism
Exosomes - pathology
Extracellular vesicles
Flow Cytometry
Humans
Hydrogen-Ion Concentration
Hypertrophy
Hypotheses
Kallikreins - blood
Male
Malignancy
Melanoma
Metastasis
Middle Aged
Nanomedicine - methods
Nanoparticles
Nanoscale flow cytometry
PCa and BPH
Peripheral blood
Physiology
Plasma
Predictive Value of Tests
Prognosis
Prostate cancer
Prostate-Specific Antigen - blood
Prostatic Neoplasms - blood
Prostatic Neoplasms - pathology
Proteins
PSA
Quantitation
Tumor Microenvironment
Tumors
Up-Regulation
Vesicles
Title Increased PSA expression on prostate cancer exosomes in in vitro condition and in cancer patients
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https://dx.doi.org/10.1016/j.canlet.2017.06.036
https://www.ncbi.nlm.nih.gov/pubmed/28694142
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