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Extracellular vesicles: the next generation of biomarkers for liquid biopsy-based prostate cancer diagnosis

Prostate cancer (PCa) is a leading cause of cancer death for males in western countries. The current gold standard for PCa diagnosis - template needle biopsies - often does not convey a true representation of the molecular profile given sampling error and complex tumour heterogeneity. Presently avai...

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Autores principales: Pang, Bairen, Zhu, Ying, Ni, Jie, Thompson, James, Malouf, David, Bucci, Joseph, Graham, Peter, Li, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7019149/
https://www.ncbi.nlm.nih.gov/pubmed/32089744
http://dx.doi.org/10.7150/thno.39486
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author Pang, Bairen
Zhu, Ying
Ni, Jie
Thompson, James
Malouf, David
Bucci, Joseph
Graham, Peter
Li, Yong
author_facet Pang, Bairen
Zhu, Ying
Ni, Jie
Thompson, James
Malouf, David
Bucci, Joseph
Graham, Peter
Li, Yong
author_sort Pang, Bairen
collection PubMed
description Prostate cancer (PCa) is a leading cause of cancer death for males in western countries. The current gold standard for PCa diagnosis - template needle biopsies - often does not convey a true representation of the molecular profile given sampling error and complex tumour heterogeneity. Presently available biomarker blood tests have limited accuracy. There is a growing demand for novel diagnostic approaches to reduce both the number of men with an abnormal PSA/ DRE who undergo invasive biopsy and the number of cores collected per biopsy. 'Liquid biopsy' is a minimally invasive biofluid-based approach that has the potential to provide information and improve the accuracy of diagnosis for patients' treatment selection, prognostic counselling and development of risk-adjusted follow-up protocols. Extracellular vesicles (EVs) are lipid bilayer-delimited particles released by tumour cells which may provide a real-time snapshot of the entire tumour in a non-invasive way. EVs can regulate physiological processes and mediate systemic dissemination of various types of cancers. Emerging evidence suggests that EVs have crucial roles in PCa development and metastasis. Most importantly, EVs are directly derived from their parent cells with their information. EVs contain components including proteins, mRNAs, DNA fragments, non-coding RNAs and lipids, and play a critical role in intercellular communication. Therefore, EVs hold promise for the discovery of liquid biopsy-based biomarkers for PCa diagnosis. Here, we review the current approaches for EV isolation and analysis, summarise the recent advances in EV protein biomarkers in PCa and focus on liquid biopsy-based EV biomarkers in PCa diagnosis for personalised medicine.
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spelling pubmed-70191492020-02-23 Extracellular vesicles: the next generation of biomarkers for liquid biopsy-based prostate cancer diagnosis Pang, Bairen Zhu, Ying Ni, Jie Thompson, James Malouf, David Bucci, Joseph Graham, Peter Li, Yong Theranostics Review Prostate cancer (PCa) is a leading cause of cancer death for males in western countries. The current gold standard for PCa diagnosis - template needle biopsies - often does not convey a true representation of the molecular profile given sampling error and complex tumour heterogeneity. Presently available biomarker blood tests have limited accuracy. There is a growing demand for novel diagnostic approaches to reduce both the number of men with an abnormal PSA/ DRE who undergo invasive biopsy and the number of cores collected per biopsy. 'Liquid biopsy' is a minimally invasive biofluid-based approach that has the potential to provide information and improve the accuracy of diagnosis for patients' treatment selection, prognostic counselling and development of risk-adjusted follow-up protocols. Extracellular vesicles (EVs) are lipid bilayer-delimited particles released by tumour cells which may provide a real-time snapshot of the entire tumour in a non-invasive way. EVs can regulate physiological processes and mediate systemic dissemination of various types of cancers. Emerging evidence suggests that EVs have crucial roles in PCa development and metastasis. Most importantly, EVs are directly derived from their parent cells with their information. EVs contain components including proteins, mRNAs, DNA fragments, non-coding RNAs and lipids, and play a critical role in intercellular communication. Therefore, EVs hold promise for the discovery of liquid biopsy-based biomarkers for PCa diagnosis. Here, we review the current approaches for EV isolation and analysis, summarise the recent advances in EV protein biomarkers in PCa and focus on liquid biopsy-based EV biomarkers in PCa diagnosis for personalised medicine. Ivyspring International Publisher 2020-01-16 /pmc/articles/PMC7019149/ /pubmed/32089744 http://dx.doi.org/10.7150/thno.39486 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Review
Pang, Bairen
Zhu, Ying
Ni, Jie
Thompson, James
Malouf, David
Bucci, Joseph
Graham, Peter
Li, Yong
Extracellular vesicles: the next generation of biomarkers for liquid biopsy-based prostate cancer diagnosis
title Extracellular vesicles: the next generation of biomarkers for liquid biopsy-based prostate cancer diagnosis
title_full Extracellular vesicles: the next generation of biomarkers for liquid biopsy-based prostate cancer diagnosis
title_fullStr Extracellular vesicles: the next generation of biomarkers for liquid biopsy-based prostate cancer diagnosis
title_full_unstemmed Extracellular vesicles: the next generation of biomarkers for liquid biopsy-based prostate cancer diagnosis
title_short Extracellular vesicles: the next generation of biomarkers for liquid biopsy-based prostate cancer diagnosis
title_sort extracellular vesicles: the next generation of biomarkers for liquid biopsy-based prostate cancer diagnosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7019149/
https://www.ncbi.nlm.nih.gov/pubmed/32089744
http://dx.doi.org/10.7150/thno.39486
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