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A simple and available measurement of onco-sEV dsDNA to protein ratio as a potential tumor marker
BACKGROUND: Small extracellular vesicles (sEVs) have great potential as new biomarkers in liquid biopsy. However, due to the limitations of sEVs extraction and component analysis procedures, further clinical applications of sEVs are hampered. Carcinoembryonic antigen (CEA) is a commonly used broad-s...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316596/ https://www.ncbi.nlm.nih.gov/pubmed/37400751 http://dx.doi.org/10.1186/s12885-023-10886-3 |
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author | Sun, Yifan Li, Miao Zhang, Xiaoshan Xu, Dongjie Wu, Jie Gu, Xinrui Khan, Adeel Shen, Han Li, Zhiyang |
author_facet | Sun, Yifan Li, Miao Zhang, Xiaoshan Xu, Dongjie Wu, Jie Gu, Xinrui Khan, Adeel Shen, Han Li, Zhiyang |
author_sort | Sun, Yifan |
collection | PubMed |
description | BACKGROUND: Small extracellular vesicles (sEVs) have great potential as new biomarkers in liquid biopsy. However, due to the limitations of sEVs extraction and component analysis procedures, further clinical applications of sEVs are hampered. Carcinoembryonic antigen (CEA) is a commonly used broad-spectrum tumor marker that is strongly expressed in a variety of malignancies. RESULTS: In this study, CEA(+) sEVs were directly separated from serum using immunomagnetic beads, and the nucleic acid to protein ultraviolet absorption ratio (NPr) of CEA(+) sEVs was determined. It was found that the NPr of CEA(+) sEVs in tumor group was higher than that of healthy group. We further analyzed the sEV-derived nucleic acid components using fluorescent staining and found that the concentration ratio of double-stranded DNA to protein (dsDPr) in CEA(+) sEVs was also significantly different between the two groups, with a sensitivity of 100% and a specificity of 41.67% for the diagnosis of pan-cancer. The AUC of dsDPr combined with NPr was 0.87 and the ACU of dsDPr combined with CA242 could reach 0.94, showing good diagnostic performance for pan-cancer. CONCLUSIONS: This study demonstrates that the dsDPr of CEA(+) sEVs can effectively distinguish sEVs derived from tumor patients and healthy individuals, which can be employed as a simple and cost-effective non-invasive screening technology to assist tumor diagnosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-10886-3. |
format | Online Article Text |
id | pubmed-10316596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103165962023-07-04 A simple and available measurement of onco-sEV dsDNA to protein ratio as a potential tumor marker Sun, Yifan Li, Miao Zhang, Xiaoshan Xu, Dongjie Wu, Jie Gu, Xinrui Khan, Adeel Shen, Han Li, Zhiyang BMC Cancer Research BACKGROUND: Small extracellular vesicles (sEVs) have great potential as new biomarkers in liquid biopsy. However, due to the limitations of sEVs extraction and component analysis procedures, further clinical applications of sEVs are hampered. Carcinoembryonic antigen (CEA) is a commonly used broad-spectrum tumor marker that is strongly expressed in a variety of malignancies. RESULTS: In this study, CEA(+) sEVs were directly separated from serum using immunomagnetic beads, and the nucleic acid to protein ultraviolet absorption ratio (NPr) of CEA(+) sEVs was determined. It was found that the NPr of CEA(+) sEVs in tumor group was higher than that of healthy group. We further analyzed the sEV-derived nucleic acid components using fluorescent staining and found that the concentration ratio of double-stranded DNA to protein (dsDPr) in CEA(+) sEVs was also significantly different between the two groups, with a sensitivity of 100% and a specificity of 41.67% for the diagnosis of pan-cancer. The AUC of dsDPr combined with NPr was 0.87 and the ACU of dsDPr combined with CA242 could reach 0.94, showing good diagnostic performance for pan-cancer. CONCLUSIONS: This study demonstrates that the dsDPr of CEA(+) sEVs can effectively distinguish sEVs derived from tumor patients and healthy individuals, which can be employed as a simple and cost-effective non-invasive screening technology to assist tumor diagnosis. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-10886-3. BioMed Central 2023-07-03 /pmc/articles/PMC10316596/ /pubmed/37400751 http://dx.doi.org/10.1186/s12885-023-10886-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Sun, Yifan Li, Miao Zhang, Xiaoshan Xu, Dongjie Wu, Jie Gu, Xinrui Khan, Adeel Shen, Han Li, Zhiyang A simple and available measurement of onco-sEV dsDNA to protein ratio as a potential tumor marker |
title | A simple and available measurement of onco-sEV dsDNA to protein ratio as a potential tumor marker |
title_full | A simple and available measurement of onco-sEV dsDNA to protein ratio as a potential tumor marker |
title_fullStr | A simple and available measurement of onco-sEV dsDNA to protein ratio as a potential tumor marker |
title_full_unstemmed | A simple and available measurement of onco-sEV dsDNA to protein ratio as a potential tumor marker |
title_short | A simple and available measurement of onco-sEV dsDNA to protein ratio as a potential tumor marker |
title_sort | simple and available measurement of onco-sev dsdna to protein ratio as a potential tumor marker |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316596/ https://www.ncbi.nlm.nih.gov/pubmed/37400751 http://dx.doi.org/10.1186/s12885-023-10886-3 |
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