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Clinical application of a microfluidic chip for immunocapture and quantification of circulating exosomes to assist breast cancer diagnosis and molecular classification
Increasing attention has been attracted by exosomes in blood-based diagnosis because cancer cells release more exosomes in serum than normal cells and these exosomes overexpress a certain number of cancer-related biomarkers. However, capture and biomarker analysis of exosomes for clinical applicatio...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5378374/ https://www.ncbi.nlm.nih.gov/pubmed/28369094 http://dx.doi.org/10.1371/journal.pone.0175050 |
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author | Fang, Shimeng Tian, Hongzhu Li, Xiancheng Jin, Dong Li, Xiaojie Kong, Jing Yang, Chun Yang, Xuesong Lu, Yao Luo, Yong Lin, Bingcheng Niu, Weidong Liu, Tingjiao |
author_facet | Fang, Shimeng Tian, Hongzhu Li, Xiancheng Jin, Dong Li, Xiaojie Kong, Jing Yang, Chun Yang, Xuesong Lu, Yao Luo, Yong Lin, Bingcheng Niu, Weidong Liu, Tingjiao |
author_sort | Fang, Shimeng |
collection | PubMed |
description | Increasing attention has been attracted by exosomes in blood-based diagnosis because cancer cells release more exosomes in serum than normal cells and these exosomes overexpress a certain number of cancer-related biomarkers. However, capture and biomarker analysis of exosomes for clinical application are technically challenging. In this study, we developed a microfluidic chip for immunocapture and quantification of circulating exosomes from small sample volume and applied this device in clinical study. Circulating EpCAM-positive exosomes were measured in 6 cases breast cancer patients and 3 healthy controls to assist diagnosis. A significant increase in the EpCAM-positive exosome level in these patients was detected, compared to healthy controls. Furthermore, we quantified circulating HER2-positive exosomes in 19 cases of breast cancer patients for molecular classification. We demonstrated that the exosomal HER2 expression levels were almost consistent with that in tumor tissues assessed by immunohistochemical staining. The microfluidic chip might provide a new platform to assist breast cancer diagnosis and molecular classification. |
format | Online Article Text |
id | pubmed-5378374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-53783742017-04-07 Clinical application of a microfluidic chip for immunocapture and quantification of circulating exosomes to assist breast cancer diagnosis and molecular classification Fang, Shimeng Tian, Hongzhu Li, Xiancheng Jin, Dong Li, Xiaojie Kong, Jing Yang, Chun Yang, Xuesong Lu, Yao Luo, Yong Lin, Bingcheng Niu, Weidong Liu, Tingjiao PLoS One Research Article Increasing attention has been attracted by exosomes in blood-based diagnosis because cancer cells release more exosomes in serum than normal cells and these exosomes overexpress a certain number of cancer-related biomarkers. However, capture and biomarker analysis of exosomes for clinical application are technically challenging. In this study, we developed a microfluidic chip for immunocapture and quantification of circulating exosomes from small sample volume and applied this device in clinical study. Circulating EpCAM-positive exosomes were measured in 6 cases breast cancer patients and 3 healthy controls to assist diagnosis. A significant increase in the EpCAM-positive exosome level in these patients was detected, compared to healthy controls. Furthermore, we quantified circulating HER2-positive exosomes in 19 cases of breast cancer patients for molecular classification. We demonstrated that the exosomal HER2 expression levels were almost consistent with that in tumor tissues assessed by immunohistochemical staining. The microfluidic chip might provide a new platform to assist breast cancer diagnosis and molecular classification. Public Library of Science 2017-04-03 /pmc/articles/PMC5378374/ /pubmed/28369094 http://dx.doi.org/10.1371/journal.pone.0175050 Text en © 2017 Fang 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Fang, Shimeng Tian, Hongzhu Li, Xiancheng Jin, Dong Li, Xiaojie Kong, Jing Yang, Chun Yang, Xuesong Lu, Yao Luo, Yong Lin, Bingcheng Niu, Weidong Liu, Tingjiao Clinical application of a microfluidic chip for immunocapture and quantification of circulating exosomes to assist breast cancer diagnosis and molecular classification |
title | Clinical application of a microfluidic chip for immunocapture and quantification of circulating exosomes to assist breast cancer diagnosis and molecular classification |
title_full | Clinical application of a microfluidic chip for immunocapture and quantification of circulating exosomes to assist breast cancer diagnosis and molecular classification |
title_fullStr | Clinical application of a microfluidic chip for immunocapture and quantification of circulating exosomes to assist breast cancer diagnosis and molecular classification |
title_full_unstemmed | Clinical application of a microfluidic chip for immunocapture and quantification of circulating exosomes to assist breast cancer diagnosis and molecular classification |
title_short | Clinical application of a microfluidic chip for immunocapture and quantification of circulating exosomes to assist breast cancer diagnosis and molecular classification |
title_sort | clinical application of a microfluidic chip for immunocapture and quantification of circulating exosomes to assist breast cancer diagnosis and molecular classification |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5378374/ https://www.ncbi.nlm.nih.gov/pubmed/28369094 http://dx.doi.org/10.1371/journal.pone.0175050 |
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