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Plasma extracellular vesicles detected by Single Molecule array technology as a liquid biopsy for colorectal cancer
Circulating extracellular vesicles (EVs) were recognized as a promising source of diagnostic biomarker. However, there are limited studies published in this area, partly due to the limited number of detection platforms capable of detecting extracellular vesicles. In this study, extracellular vesicle...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480466/ https://www.ncbi.nlm.nih.gov/pubmed/32944195 http://dx.doi.org/10.1080/20013078.2020.1809765 |
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author | Wei, Ping Wu, Fei Kang, Bin Sun, Xiaohua Heskia, Fabienne Pachot, Alexandre Liang, Ji Li, Dawei |
author_facet | Wei, Ping Wu, Fei Kang, Bin Sun, Xiaohua Heskia, Fabienne Pachot, Alexandre Liang, Ji Li, Dawei |
author_sort | Wei, Ping |
collection | PubMed |
description | Circulating extracellular vesicles (EVs) were recognized as a promising source of diagnostic biomarker. However, there are limited studies published in this area, partly due to the limited number of detection platforms capable of detecting extracellular vesicles. In this study, extracellular vesicle immunoassays were developed using the Single Molecule array technology (SiMoa) and their clinical applications to cancer diagnosis were evaluated. Two extracellular vesicle detection assays, CD9-CD63 and Epcam-CD63, were designed to detect universal extracellular vesicles and tumour-derived extracellular vesicles, respectively. Our results show that CD9-CD63 and Epcam-CD63 SiMoa assays specifically detect extracellular vesicles but not free proteins with high sensitivities. The Epcam-CD63 levels detected in cancer cell culture media were consistent with levels of Epcam-expressing EVs isolated from the same cancer cell lines and detected by Western blot. Furthermore, the assays distinguish cancerous from non-cancerous plasma samples. The highest CD9-CD63 and Epcam-CD63 signals were observed in colorectal cancer patients comparing to healthy and benign controls. Both assays showed superior diagnostic performance for colorectal cancer. In addition, our results show that CD9-CD63 detection is an independent prognosis factor for both progression free survival and overall survival, while Epcam-CD63 detectionis an independent prognosis factor for OS. |
format | Online Article Text |
id | pubmed-7480466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-74804662020-09-16 Plasma extracellular vesicles detected by Single Molecule array technology as a liquid biopsy for colorectal cancer Wei, Ping Wu, Fei Kang, Bin Sun, Xiaohua Heskia, Fabienne Pachot, Alexandre Liang, Ji Li, Dawei J Extracell Vesicles Research Article Circulating extracellular vesicles (EVs) were recognized as a promising source of diagnostic biomarker. However, there are limited studies published in this area, partly due to the limited number of detection platforms capable of detecting extracellular vesicles. In this study, extracellular vesicle immunoassays were developed using the Single Molecule array technology (SiMoa) and their clinical applications to cancer diagnosis were evaluated. Two extracellular vesicle detection assays, CD9-CD63 and Epcam-CD63, were designed to detect universal extracellular vesicles and tumour-derived extracellular vesicles, respectively. Our results show that CD9-CD63 and Epcam-CD63 SiMoa assays specifically detect extracellular vesicles but not free proteins with high sensitivities. The Epcam-CD63 levels detected in cancer cell culture media were consistent with levels of Epcam-expressing EVs isolated from the same cancer cell lines and detected by Western blot. Furthermore, the assays distinguish cancerous from non-cancerous plasma samples. The highest CD9-CD63 and Epcam-CD63 signals were observed in colorectal cancer patients comparing to healthy and benign controls. Both assays showed superior diagnostic performance for colorectal cancer. In addition, our results show that CD9-CD63 detection is an independent prognosis factor for both progression free survival and overall survival, while Epcam-CD63 detectionis an independent prognosis factor for OS. Taylor & Francis 2020-08-26 /pmc/articles/PMC7480466/ /pubmed/32944195 http://dx.doi.org/10.1080/20013078.2020.1809765 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of The International Society for Extracellular Vesicles. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Wei, Ping Wu, Fei Kang, Bin Sun, Xiaohua Heskia, Fabienne Pachot, Alexandre Liang, Ji Li, Dawei Plasma extracellular vesicles detected by Single Molecule array technology as a liquid biopsy for colorectal cancer |
title | Plasma extracellular vesicles detected by Single Molecule array technology as a liquid biopsy for colorectal cancer |
title_full | Plasma extracellular vesicles detected by Single Molecule array technology as a liquid biopsy for colorectal cancer |
title_fullStr | Plasma extracellular vesicles detected by Single Molecule array technology as a liquid biopsy for colorectal cancer |
title_full_unstemmed | Plasma extracellular vesicles detected by Single Molecule array technology as a liquid biopsy for colorectal cancer |
title_short | Plasma extracellular vesicles detected by Single Molecule array technology as a liquid biopsy for colorectal cancer |
title_sort | plasma extracellular vesicles detected by single molecule array technology as a liquid biopsy for colorectal cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480466/ https://www.ncbi.nlm.nih.gov/pubmed/32944195 http://dx.doi.org/10.1080/20013078.2020.1809765 |
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