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Detection of Breast Cancer-Specific Extracellular Vesicles with Fiber-Optic SPR Biosensor

Extracellular vesicles (EVs) have attracted great attention as potential biomarkers for cancer diagnostics. Although several technologies have been developed for EV detection, many of them are still not applicable to clinical settings as they rely on complex EV isolation processes, while lacking sen...

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Autores principales: Yildizhan, Yagmur, Driessens, Kaat, Tsao, Hong Shen Kevin, Boiy, Robin, Thomas, Debby, Geukens, Nick, Hendrix, An, Lammertyn, Jeroen, Spasic, Dragana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9966403/
https://www.ncbi.nlm.nih.gov/pubmed/36835174
http://dx.doi.org/10.3390/ijms24043764
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author Yildizhan, Yagmur
Driessens, Kaat
Tsao, Hong Shen Kevin
Boiy, Robin
Thomas, Debby
Geukens, Nick
Hendrix, An
Lammertyn, Jeroen
Spasic, Dragana
author_facet Yildizhan, Yagmur
Driessens, Kaat
Tsao, Hong Shen Kevin
Boiy, Robin
Thomas, Debby
Geukens, Nick
Hendrix, An
Lammertyn, Jeroen
Spasic, Dragana
author_sort Yildizhan, Yagmur
collection PubMed
description Extracellular vesicles (EVs) have attracted great attention as potential biomarkers for cancer diagnostics. Although several technologies have been developed for EV detection, many of them are still not applicable to clinical settings as they rely on complex EV isolation processes, while lacking sensitivity, specificity or standardization. To solve this problem, we have developed a sensitive breast cancer-specific EV detection bioassay directly in blood plasma using a fiber-optic surface plasmon resonance (FO-SPR) biosensor, previously calibrated with recombinant EVs. First, we established a sandwich bioassay to detect SK-BR-3 EVs by functionalizing the FO-SPR probes with anti-HER2 antibodies. A calibration curve was built using an anti-HER2/(B)anti-CD9 combination, resulting in an LOD of 2.1 × 10(7) particles/mL in buffer and 7 × 10(8) particles/mL in blood plasma. Next, we investigated the potential of the bioassay to detect MCF7 EVs in blood plasma using an anti-EpCAM/(B)anti-mix combination, obtaining an LOD of 1.1 × 10 (8) particles/mL. Finally, the specificity of the bioassay was proven by the absence of signal when testing plasma samples from 10 healthy people unknown to be diagnosed with breast cancer. The remarkable sensitivity and specificity of the developed sandwich bioassay together with the advantages of the standardized FO-SPR biosensor highlight outstanding potential for the future of EV analysis.
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spelling pubmed-99664032023-02-26 Detection of Breast Cancer-Specific Extracellular Vesicles with Fiber-Optic SPR Biosensor Yildizhan, Yagmur Driessens, Kaat Tsao, Hong Shen Kevin Boiy, Robin Thomas, Debby Geukens, Nick Hendrix, An Lammertyn, Jeroen Spasic, Dragana Int J Mol Sci Article Extracellular vesicles (EVs) have attracted great attention as potential biomarkers for cancer diagnostics. Although several technologies have been developed for EV detection, many of them are still not applicable to clinical settings as they rely on complex EV isolation processes, while lacking sensitivity, specificity or standardization. To solve this problem, we have developed a sensitive breast cancer-specific EV detection bioassay directly in blood plasma using a fiber-optic surface plasmon resonance (FO-SPR) biosensor, previously calibrated with recombinant EVs. First, we established a sandwich bioassay to detect SK-BR-3 EVs by functionalizing the FO-SPR probes with anti-HER2 antibodies. A calibration curve was built using an anti-HER2/(B)anti-CD9 combination, resulting in an LOD of 2.1 × 10(7) particles/mL in buffer and 7 × 10(8) particles/mL in blood plasma. Next, we investigated the potential of the bioassay to detect MCF7 EVs in blood plasma using an anti-EpCAM/(B)anti-mix combination, obtaining an LOD of 1.1 × 10 (8) particles/mL. Finally, the specificity of the bioassay was proven by the absence of signal when testing plasma samples from 10 healthy people unknown to be diagnosed with breast cancer. The remarkable sensitivity and specificity of the developed sandwich bioassay together with the advantages of the standardized FO-SPR biosensor highlight outstanding potential for the future of EV analysis. MDPI 2023-02-13 /pmc/articles/PMC9966403/ /pubmed/36835174 http://dx.doi.org/10.3390/ijms24043764 Text en © 2023 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
Yildizhan, Yagmur
Driessens, Kaat
Tsao, Hong Shen Kevin
Boiy, Robin
Thomas, Debby
Geukens, Nick
Hendrix, An
Lammertyn, Jeroen
Spasic, Dragana
Detection of Breast Cancer-Specific Extracellular Vesicles with Fiber-Optic SPR Biosensor
title Detection of Breast Cancer-Specific Extracellular Vesicles with Fiber-Optic SPR Biosensor
title_full Detection of Breast Cancer-Specific Extracellular Vesicles with Fiber-Optic SPR Biosensor
title_fullStr Detection of Breast Cancer-Specific Extracellular Vesicles with Fiber-Optic SPR Biosensor
title_full_unstemmed Detection of Breast Cancer-Specific Extracellular Vesicles with Fiber-Optic SPR Biosensor
title_short Detection of Breast Cancer-Specific Extracellular Vesicles with Fiber-Optic SPR Biosensor
title_sort detection of breast cancer-specific extracellular vesicles with fiber-optic spr biosensor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9966403/
https://www.ncbi.nlm.nih.gov/pubmed/36835174
http://dx.doi.org/10.3390/ijms24043764
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