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Identification of rare cell populations in autofluorescence lifetime image data

Drug‐resistant cells and anti‐inflammatory immune cells within tumor masses contribute to tumor aggression, invasion, and worse patient outcomes. These cells can be a small proportion (<10%) of the total cell population of the tumor. Due to their small quantity, the identification of rare cells i...

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Autores principales: Cardona, Elizabeth N., Walsh, Alex J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9302681/
https://www.ncbi.nlm.nih.gov/pubmed/35038211
http://dx.doi.org/10.1002/cyto.a.24534
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author Cardona, Elizabeth N.
Walsh, Alex J.
author_facet Cardona, Elizabeth N.
Walsh, Alex J.
author_sort Cardona, Elizabeth N.
collection PubMed
description Drug‐resistant cells and anti‐inflammatory immune cells within tumor masses contribute to tumor aggression, invasion, and worse patient outcomes. These cells can be a small proportion (<10%) of the total cell population of the tumor. Due to their small quantity, the identification of rare cells is challenging with traditional assays. Single cell analysis of autofluorescence images provides a live‐cell assay to quantify cellular heterogeneity. Fluorescence intensities and lifetimes of the metabolic coenzymes reduced nicotinamide adenine dinucleotide and oxidized flavin adenine dinucleotide allow quantification of cellular metabolism and provide features for classification of cells with different metabolic phenotypes. In this study, Gaussian distribution modeling and machine learning classification algorithms are used for the identification of rare cells within simulated autofluorescence lifetime image data of a large tumor comprised of tumor cells and T cells. A Random Forest machine learning algorithm achieved an overall accuracy of 95% for the identification of cell type from the simulated optical metabolic imaging data of a heterogeneous tumor of 20,000 cells consisting of 70% drug responsive breast cancer cells, 5% drug resistant breast cancer cells, 20% quiescent T cells and 5% activated T cells. High resolution imaging methods combined with single‐cell quantitative analyses allows identification and quantification of rare populations of cells within heterogeneous cultures
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spelling pubmed-93026812022-07-22 Identification of rare cell populations in autofluorescence lifetime image data Cardona, Elizabeth N. Walsh, Alex J. Cytometry A Original Articles Drug‐resistant cells and anti‐inflammatory immune cells within tumor masses contribute to tumor aggression, invasion, and worse patient outcomes. These cells can be a small proportion (<10%) of the total cell population of the tumor. Due to their small quantity, the identification of rare cells is challenging with traditional assays. Single cell analysis of autofluorescence images provides a live‐cell assay to quantify cellular heterogeneity. Fluorescence intensities and lifetimes of the metabolic coenzymes reduced nicotinamide adenine dinucleotide and oxidized flavin adenine dinucleotide allow quantification of cellular metabolism and provide features for classification of cells with different metabolic phenotypes. In this study, Gaussian distribution modeling and machine learning classification algorithms are used for the identification of rare cells within simulated autofluorescence lifetime image data of a large tumor comprised of tumor cells and T cells. A Random Forest machine learning algorithm achieved an overall accuracy of 95% for the identification of cell type from the simulated optical metabolic imaging data of a heterogeneous tumor of 20,000 cells consisting of 70% drug responsive breast cancer cells, 5% drug resistant breast cancer cells, 20% quiescent T cells and 5% activated T cells. High resolution imaging methods combined with single‐cell quantitative analyses allows identification and quantification of rare populations of cells within heterogeneous cultures John Wiley & Sons, Inc. 2022-01-25 2022-06 /pmc/articles/PMC9302681/ /pubmed/35038211 http://dx.doi.org/10.1002/cyto.a.24534 Text en © 2022 The Authors. Cytometry Part A published by Wiley Periodicals LLC on behalf of International Society for Advancement of Cytometry. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Cardona, Elizabeth N.
Walsh, Alex J.
Identification of rare cell populations in autofluorescence lifetime image data
title Identification of rare cell populations in autofluorescence lifetime image data
title_full Identification of rare cell populations in autofluorescence lifetime image data
title_fullStr Identification of rare cell populations in autofluorescence lifetime image data
title_full_unstemmed Identification of rare cell populations in autofluorescence lifetime image data
title_short Identification of rare cell populations in autofluorescence lifetime image data
title_sort identification of rare cell populations in autofluorescence lifetime image data
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9302681/
https://www.ncbi.nlm.nih.gov/pubmed/35038211
http://dx.doi.org/10.1002/cyto.a.24534
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