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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...

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Autores principales: Vinod, Rufus, Mahran, Randa, Routila, Erica, Leivo, Janne, Pettersson, Kim, Gidwani, Kamlesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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