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Label-free flow cytometry of rare circulating tumor cell clusters in whole blood

Circulating tumor cell clusters (CTCCs) are rare cellular events found in the blood stream of metastatic tumor patients. Despite their scarcity, they represent an increased risk for metastasis. Label-free detection methods of these events remain primarily limited to in vitro microfluidic platforms....

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Autores principales: Vora, Nilay, Shekhar, Prashant, Esmail, Michael, Patra, Abani, Georgakoudi, Irene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9232518/
https://www.ncbi.nlm.nih.gov/pubmed/35750889
http://dx.doi.org/10.1038/s41598-022-14003-5
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author Vora, Nilay
Shekhar, Prashant
Esmail, Michael
Patra, Abani
Georgakoudi, Irene
author_facet Vora, Nilay
Shekhar, Prashant
Esmail, Michael
Patra, Abani
Georgakoudi, Irene
author_sort Vora, Nilay
collection PubMed
description Circulating tumor cell clusters (CTCCs) are rare cellular events found in the blood stream of metastatic tumor patients. Despite their scarcity, they represent an increased risk for metastasis. Label-free detection methods of these events remain primarily limited to in vitro microfluidic platforms. Here, we expand on the use of confocal backscatter and fluorescence flow cytometry (BSFC) for label-free detection of CTCCs in whole blood using machine learning for peak detection/classification. BSFC uses a custom-built flow cytometer with three excitation wavelengths (405 nm, 488 nm, and 633 nm) and five detectors to detect CTCCs in whole blood based on corresponding scattering and fluorescence signals. In this study, detection of CTCC-associated GFP fluorescence is used as the ground truth to assess the accuracy of endogenous back-scattered light-based CTCC detection in whole blood. Using a machine learning model for peak detection/classification, we demonstrated that the combined use of backscattered signals at the three wavelengths enable detection of ~ 93% of all CTCCs larger than two cells with a purity of > 82% and an overall accuracy of > 95%. The high level of performance established through BSFC and machine learning demonstrates the potential for label-free detection and monitoring of CTCCs in whole blood. Further developments of label-free BSFC to enhance throughput could lead to important applications in the isolation of CTCCs in whole blood with minimal disruption and ultimately their detection in vivo.
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spelling pubmed-92325182022-06-26 Label-free flow cytometry of rare circulating tumor cell clusters in whole blood Vora, Nilay Shekhar, Prashant Esmail, Michael Patra, Abani Georgakoudi, Irene Sci Rep Article Circulating tumor cell clusters (CTCCs) are rare cellular events found in the blood stream of metastatic tumor patients. Despite their scarcity, they represent an increased risk for metastasis. Label-free detection methods of these events remain primarily limited to in vitro microfluidic platforms. Here, we expand on the use of confocal backscatter and fluorescence flow cytometry (BSFC) for label-free detection of CTCCs in whole blood using machine learning for peak detection/classification. BSFC uses a custom-built flow cytometer with three excitation wavelengths (405 nm, 488 nm, and 633 nm) and five detectors to detect CTCCs in whole blood based on corresponding scattering and fluorescence signals. In this study, detection of CTCC-associated GFP fluorescence is used as the ground truth to assess the accuracy of endogenous back-scattered light-based CTCC detection in whole blood. Using a machine learning model for peak detection/classification, we demonstrated that the combined use of backscattered signals at the three wavelengths enable detection of ~ 93% of all CTCCs larger than two cells with a purity of > 82% and an overall accuracy of > 95%. The high level of performance established through BSFC and machine learning demonstrates the potential for label-free detection and monitoring of CTCCs in whole blood. Further developments of label-free BSFC to enhance throughput could lead to important applications in the isolation of CTCCs in whole blood with minimal disruption and ultimately their detection in vivo. Nature Publishing Group UK 2022-06-24 /pmc/articles/PMC9232518/ /pubmed/35750889 http://dx.doi.org/10.1038/s41598-022-14003-5 Text en © The Author(s) 2022 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/) .
spellingShingle Article
Vora, Nilay
Shekhar, Prashant
Esmail, Michael
Patra, Abani
Georgakoudi, Irene
Label-free flow cytometry of rare circulating tumor cell clusters in whole blood
title Label-free flow cytometry of rare circulating tumor cell clusters in whole blood
title_full Label-free flow cytometry of rare circulating tumor cell clusters in whole blood
title_fullStr Label-free flow cytometry of rare circulating tumor cell clusters in whole blood
title_full_unstemmed Label-free flow cytometry of rare circulating tumor cell clusters in whole blood
title_short Label-free flow cytometry of rare circulating tumor cell clusters in whole blood
title_sort label-free flow cytometry of rare circulating tumor cell clusters in whole blood
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9232518/
https://www.ncbi.nlm.nih.gov/pubmed/35750889
http://dx.doi.org/10.1038/s41598-022-14003-5
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