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Nanoparticle-Aided Detection of Colorectal Cancer-Associated Glycoconjugates of Extracellular Vesicles in Human Serum
Extracellular vesicles (EVs) are found in all biological fluids, providing potential for the identification of disease biomarkers such as colorectal cancer (CRC). EVs are heavily glycosylated with specific glycoconjugates such as tetraspanins, integrins, and mucins, reflecting the characteristics of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8508761/ https://www.ncbi.nlm.nih.gov/pubmed/34638669 http://dx.doi.org/10.3390/ijms221910329 |
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author | Vinod, Rufus Mahran, Randa Routila, Erica Leivo, Janne Pettersson, Kim Gidwani, Kamlesh |
author_facet | Vinod, Rufus Mahran, Randa Routila, Erica Leivo, Janne Pettersson, Kim Gidwani, Kamlesh |
author_sort | Vinod, Rufus |
collection | PubMed |
description | Extracellular vesicles (EVs) are found in all biological fluids, providing potential for the identification of disease biomarkers such as colorectal cancer (CRC). EVs are heavily glycosylated with specific glycoconjugates such as tetraspanins, integrins, and mucins, reflecting the characteristics of the original cell offering valuable targets for detection of CRC. We report here on europium-nanoparticle (EuNP)-based assay to detect and characterize different surface glycoconjugates of EVs without extensive purification steps from five different CRC and the HEK 293 cell lines. The promising EVs candidates from cell culture were clinically evaluated on small panel of serum samples including early-stage (n = 11) and late-stage (n = 11) CRC patients, benign condition (n = 11), and healthy control (n = 10). The majority of CRC cell lines expressed tetraspanin sub-population and glycovariants of integrins and conventional tumor markers. The subpopulation of CD151 having CD63 expression (CD151(CD63)) was significantly (p = 0.001) elevated in early-stage CRC (8 out of 11) without detecting any benign and late-stage samples, while conventional CEA detected mostly late-stage CRC (p = 0.045) and with only four early-stage cases. The other glycovariant assays such as CEA(Con-A), CA125(WGA), CA 19.9(Ma696), and CA 19.9(Con-A) further provided some complementation to the CD151(CD63) assay. These results indicate the potential application of CD151(CD63) assay for early detection of CRC patients in human serum. |
format | Online Article Text |
id | pubmed-8508761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85087612021-10-13 Nanoparticle-Aided Detection of Colorectal Cancer-Associated Glycoconjugates of Extracellular Vesicles in Human Serum Vinod, Rufus Mahran, Randa Routila, Erica Leivo, Janne Pettersson, Kim Gidwani, Kamlesh Int J Mol Sci Article Extracellular vesicles (EVs) are found in all biological fluids, providing potential for the identification of disease biomarkers such as colorectal cancer (CRC). EVs are heavily glycosylated with specific glycoconjugates such as tetraspanins, integrins, and mucins, reflecting the characteristics of the original cell offering valuable targets for detection of CRC. We report here on europium-nanoparticle (EuNP)-based assay to detect and characterize different surface glycoconjugates of EVs without extensive purification steps from five different CRC and the HEK 293 cell lines. The promising EVs candidates from cell culture were clinically evaluated on small panel of serum samples including early-stage (n = 11) and late-stage (n = 11) CRC patients, benign condition (n = 11), and healthy control (n = 10). The majority of CRC cell lines expressed tetraspanin sub-population and glycovariants of integrins and conventional tumor markers. The subpopulation of CD151 having CD63 expression (CD151(CD63)) was significantly (p = 0.001) elevated in early-stage CRC (8 out of 11) without detecting any benign and late-stage samples, while conventional CEA detected mostly late-stage CRC (p = 0.045) and with only four early-stage cases. The other glycovariant assays such as CEA(Con-A), CA125(WGA), CA 19.9(Ma696), and CA 19.9(Con-A) further provided some complementation to the CD151(CD63) assay. These results indicate the potential application of CD151(CD63) assay for early detection of CRC patients in human serum. MDPI 2021-09-25 /pmc/articles/PMC8508761/ /pubmed/34638669 http://dx.doi.org/10.3390/ijms221910329 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Vinod, Rufus Mahran, Randa Routila, Erica Leivo, Janne Pettersson, Kim Gidwani, Kamlesh Nanoparticle-Aided Detection of Colorectal Cancer-Associated Glycoconjugates of Extracellular Vesicles in Human Serum |
title | Nanoparticle-Aided Detection of Colorectal Cancer-Associated Glycoconjugates of Extracellular Vesicles in Human Serum |
title_full | Nanoparticle-Aided Detection of Colorectal Cancer-Associated Glycoconjugates of Extracellular Vesicles in Human Serum |
title_fullStr | Nanoparticle-Aided Detection of Colorectal Cancer-Associated Glycoconjugates of Extracellular Vesicles in Human Serum |
title_full_unstemmed | Nanoparticle-Aided Detection of Colorectal Cancer-Associated Glycoconjugates of Extracellular Vesicles in Human Serum |
title_short | Nanoparticle-Aided Detection of Colorectal Cancer-Associated Glycoconjugates of Extracellular Vesicles in Human Serum |
title_sort | nanoparticle-aided detection of colorectal cancer-associated glycoconjugates of extracellular vesicles in human serum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8508761/ https://www.ncbi.nlm.nih.gov/pubmed/34638669 http://dx.doi.org/10.3390/ijms221910329 |
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