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Facile preparation of salivary extracellular vesicles for cancer proteomics

Extracellular vesicles (EVs) are membrane surrounded structures released by cells, which have been increasingly recognized as mediators of intercellular communication. Recent reports indicate that EVs participate in important biological processes and could serve as potential source for cancer biomar...

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Autores principales: Sun, Yan, Xia, Zhijun, Shang, Zhi, Sun, Kaibo, Niu, Xiaomin, Qian, Liqiang, Fan, Liu-Yin, Cao, Cheng-Xi, Xiao, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835767/
https://www.ncbi.nlm.nih.gov/pubmed/27091080
http://dx.doi.org/10.1038/srep24669
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author Sun, Yan
Xia, Zhijun
Shang, Zhi
Sun, Kaibo
Niu, Xiaomin
Qian, Liqiang
Fan, Liu-Yin
Cao, Cheng-Xi
Xiao, Hua
author_facet Sun, Yan
Xia, Zhijun
Shang, Zhi
Sun, Kaibo
Niu, Xiaomin
Qian, Liqiang
Fan, Liu-Yin
Cao, Cheng-Xi
Xiao, Hua
author_sort Sun, Yan
collection PubMed
description Extracellular vesicles (EVs) are membrane surrounded structures released by cells, which have been increasingly recognized as mediators of intercellular communication. Recent reports indicate that EVs participate in important biological processes and could serve as potential source for cancer biomarkers. As an attractive EVs source with merit of non-invasiveness, human saliva is a unique medium for clinical diagnostics. Thus, we proposed a facile approach to prepare salivary extracellular vesicles (SEVs). Affinity chromatography column combined with filter system (ACCF) was developed to efficiently remove the high abundant proteins and viscous interferences of saliva. Protein profiling in the SEVs obtained by this strategy was compared with conventional centrifugation method, which demonstrated that about 70% more SEVs proteins could be revealed. To explore its utility for cancer proteomics, we analyzed the proteome of SEVs in lung cancer patients and normal controls. Shotgun proteomic analysis illustrated that 113 and 95 proteins have been identified in cancer group and control group, respectively. Among those 63 proteins that have been consistently discovered only in cancer group, 12 proteins are lung cancer related. Our results demonstrated that SEVs prepared through the developed strategy are valuable samples for proteomics and could serve as a promising liquid biopsy for cancer.
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spelling pubmed-48357672016-04-27 Facile preparation of salivary extracellular vesicles for cancer proteomics Sun, Yan Xia, Zhijun Shang, Zhi Sun, Kaibo Niu, Xiaomin Qian, Liqiang Fan, Liu-Yin Cao, Cheng-Xi Xiao, Hua Sci Rep Article Extracellular vesicles (EVs) are membrane surrounded structures released by cells, which have been increasingly recognized as mediators of intercellular communication. Recent reports indicate that EVs participate in important biological processes and could serve as potential source for cancer biomarkers. As an attractive EVs source with merit of non-invasiveness, human saliva is a unique medium for clinical diagnostics. Thus, we proposed a facile approach to prepare salivary extracellular vesicles (SEVs). Affinity chromatography column combined with filter system (ACCF) was developed to efficiently remove the high abundant proteins and viscous interferences of saliva. Protein profiling in the SEVs obtained by this strategy was compared with conventional centrifugation method, which demonstrated that about 70% more SEVs proteins could be revealed. To explore its utility for cancer proteomics, we analyzed the proteome of SEVs in lung cancer patients and normal controls. Shotgun proteomic analysis illustrated that 113 and 95 proteins have been identified in cancer group and control group, respectively. Among those 63 proteins that have been consistently discovered only in cancer group, 12 proteins are lung cancer related. Our results demonstrated that SEVs prepared through the developed strategy are valuable samples for proteomics and could serve as a promising liquid biopsy for cancer. Nature Publishing Group 2016-04-19 /pmc/articles/PMC4835767/ /pubmed/27091080 http://dx.doi.org/10.1038/srep24669 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Sun, Yan
Xia, Zhijun
Shang, Zhi
Sun, Kaibo
Niu, Xiaomin
Qian, Liqiang
Fan, Liu-Yin
Cao, Cheng-Xi
Xiao, Hua
Facile preparation of salivary extracellular vesicles for cancer proteomics
title Facile preparation of salivary extracellular vesicles for cancer proteomics
title_full Facile preparation of salivary extracellular vesicles for cancer proteomics
title_fullStr Facile preparation of salivary extracellular vesicles for cancer proteomics
title_full_unstemmed Facile preparation of salivary extracellular vesicles for cancer proteomics
title_short Facile preparation of salivary extracellular vesicles for cancer proteomics
title_sort facile preparation of salivary extracellular vesicles for cancer proteomics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835767/
https://www.ncbi.nlm.nih.gov/pubmed/27091080
http://dx.doi.org/10.1038/srep24669
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