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Plasma-Derived Exosomal Survivin, a Plausible Biomarker for Early Detection of Prostate Cancer
BACKGROUND: Survivin is expressed in prostate cancer (PCa), and its downregulation sensitizes PCa cells to chemotherapeutic agents in vitro and in vivo. Small membrane-bound vesicles called exosomes, secreted from the endosomal membrane compartment, contain RNA and protein that they readily transpor...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3473028/ https://www.ncbi.nlm.nih.gov/pubmed/23091600 http://dx.doi.org/10.1371/journal.pone.0046737 |
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author | Khan, Salma Jutzy, Jessica M. S. Valenzuela, Malyn May A. Turay, David Aspe, Jonathan R. Ashok, Arjun Mirshahidi, Saied Mercola, Dan Lilly, Michael B. Wall, Nathan R. |
author_facet | Khan, Salma Jutzy, Jessica M. S. Valenzuela, Malyn May A. Turay, David Aspe, Jonathan R. Ashok, Arjun Mirshahidi, Saied Mercola, Dan Lilly, Michael B. Wall, Nathan R. |
author_sort | Khan, Salma |
collection | PubMed |
description | BACKGROUND: Survivin is expressed in prostate cancer (PCa), and its downregulation sensitizes PCa cells to chemotherapeutic agents in vitro and in vivo. Small membrane-bound vesicles called exosomes, secreted from the endosomal membrane compartment, contain RNA and protein that they readily transport via exosome internalization into recipient cells. Recent progress has shown that tumor-derived exosomes play multiple roles in tumor growth and metastasis and may produce these functions via immune escape, tumor invasion and angiogenesis. Furthermore, exosome analysis may provide novel biomarkers to diagnose or monitor PCa treatment. METHODS: Exosomes were purified from the plasma and serum from 39 PCa patients, 20 BPH patients, 8 prostate cancer recurrent and 16 healthy controls using ultracentrifugation and their quantities and qualities were quantified and visualized from both the plasma and the purified exosomes using ELISA and Western blotting, respectively. RESULTS: Survivin was significantly increased in the tumor-derived samples, compared to those from BPH and controls with virtually no difference in the quantity of Survivin detected in exosomes collected from newly diagnosed patients exhibiting low (six) or high (nine) Gleason scores. Exosome Survivin levels were also higher in patients that had relapsed on chemotherapy compared to controls. CONCLUSIONS: These studies demonstrate that Survivin exists in plasma exosomes from both normal, BPH and PCa subjects. The relative amounts of exosomal Survivin in PCa plasma was significantly higher than in those with pre-inflammatory BPH and control plasma. This differential expression of exosomal Survivin was seen with both newly diagnosed and advanced PCa subjects with high or low-grade cancers. Analysis of plasma exosomal Survivin levels may offer a convenient tool for diagnosing or monitoring PCa and may, as it is elevated in low as well as high Gleason scored samples, be used for early detection. |
format | Online Article Text |
id | pubmed-3473028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34730282012-10-22 Plasma-Derived Exosomal Survivin, a Plausible Biomarker for Early Detection of Prostate Cancer Khan, Salma Jutzy, Jessica M. S. Valenzuela, Malyn May A. Turay, David Aspe, Jonathan R. Ashok, Arjun Mirshahidi, Saied Mercola, Dan Lilly, Michael B. Wall, Nathan R. PLoS One Research Article BACKGROUND: Survivin is expressed in prostate cancer (PCa), and its downregulation sensitizes PCa cells to chemotherapeutic agents in vitro and in vivo. Small membrane-bound vesicles called exosomes, secreted from the endosomal membrane compartment, contain RNA and protein that they readily transport via exosome internalization into recipient cells. Recent progress has shown that tumor-derived exosomes play multiple roles in tumor growth and metastasis and may produce these functions via immune escape, tumor invasion and angiogenesis. Furthermore, exosome analysis may provide novel biomarkers to diagnose or monitor PCa treatment. METHODS: Exosomes were purified from the plasma and serum from 39 PCa patients, 20 BPH patients, 8 prostate cancer recurrent and 16 healthy controls using ultracentrifugation and their quantities and qualities were quantified and visualized from both the plasma and the purified exosomes using ELISA and Western blotting, respectively. RESULTS: Survivin was significantly increased in the tumor-derived samples, compared to those from BPH and controls with virtually no difference in the quantity of Survivin detected in exosomes collected from newly diagnosed patients exhibiting low (six) or high (nine) Gleason scores. Exosome Survivin levels were also higher in patients that had relapsed on chemotherapy compared to controls. CONCLUSIONS: These studies demonstrate that Survivin exists in plasma exosomes from both normal, BPH and PCa subjects. The relative amounts of exosomal Survivin in PCa plasma was significantly higher than in those with pre-inflammatory BPH and control plasma. This differential expression of exosomal Survivin was seen with both newly diagnosed and advanced PCa subjects with high or low-grade cancers. Analysis of plasma exosomal Survivin levels may offer a convenient tool for diagnosing or monitoring PCa and may, as it is elevated in low as well as high Gleason scored samples, be used for early detection. Public Library of Science 2012-10-16 /pmc/articles/PMC3473028/ /pubmed/23091600 http://dx.doi.org/10.1371/journal.pone.0046737 Text en © 2012 Khan et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited. |
spellingShingle | Research Article Khan, Salma Jutzy, Jessica M. S. Valenzuela, Malyn May A. Turay, David Aspe, Jonathan R. Ashok, Arjun Mirshahidi, Saied Mercola, Dan Lilly, Michael B. Wall, Nathan R. Plasma-Derived Exosomal Survivin, a Plausible Biomarker for Early Detection of Prostate Cancer |
title | Plasma-Derived Exosomal Survivin, a Plausible Biomarker for Early Detection of Prostate Cancer |
title_full | Plasma-Derived Exosomal Survivin, a Plausible Biomarker for Early Detection of Prostate Cancer |
title_fullStr | Plasma-Derived Exosomal Survivin, a Plausible Biomarker for Early Detection of Prostate Cancer |
title_full_unstemmed | Plasma-Derived Exosomal Survivin, a Plausible Biomarker for Early Detection of Prostate Cancer |
title_short | Plasma-Derived Exosomal Survivin, a Plausible Biomarker for Early Detection of Prostate Cancer |
title_sort | plasma-derived exosomal survivin, a plausible biomarker for early detection of prostate cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3473028/ https://www.ncbi.nlm.nih.gov/pubmed/23091600 http://dx.doi.org/10.1371/journal.pone.0046737 |
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