Cell-morphodynamic phenotype classification with application to cancer metastasis using cell magnetorotation and machine-learning

We define cell morphodynamics as the cell’s time dependent morphology. It could be called the cell’s shape shifting ability. To measure it we use a biomarker free, dynamic histology method, which is based on multiplexed Cell Magneto-Rotation and Machine Learning. We note that standard studies lookin...

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Autores principales: Remy Elbez, Jeff Folz, Alan McLean, Hernan Roca, Joseph M. Labuz, Kenneth J. Pienta, Shuichi Takayama, Raoul Kopelman
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Publicado: Public Library of Science (PLoS) 2021
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Acceso en línea:https://doaj.org/article/fdb6ebe73a384d29930d6889ca7e3b22
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spelling oai:doaj.org-article:fdb6ebe73a384d29930d6889ca7e3b222021-11-25T06:13:54ZCell-morphodynamic phenotype classification with application to cancer metastasis using cell magnetorotation and machine-learning1932-6203https://doaj.org/article/fdb6ebe73a384d29930d6889ca7e3b222021-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8598033/?tool=EBIhttps://doaj.org/toc/1932-6203We define cell morphodynamics as the cell’s time dependent morphology. It could be called the cell’s shape shifting ability. To measure it we use a biomarker free, dynamic histology method, which is based on multiplexed Cell Magneto-Rotation and Machine Learning. We note that standard studies looking at cells immobilized on microscope slides cannot reveal their shape shifting, no more than pinned butterfly collections can reveal their flight patterns. Using cell magnetorotation, with the aid of cell embedded magnetic nanoparticles, our method allows each cell to move freely in 3 dimensions, with a rapid following of cell deformations in all 3-dimensions, so as to identify and classify a cell by its dynamic morphology. Using object recognition and machine learning algorithms, we continuously measure the real-time shape dynamics of each cell, where from we successfully resolve the inherent broad heterogeneity of the morphological phenotypes found in a given cancer cell population. In three illustrative experiments we have achieved clustering, differentiation, and identification of cells from (A) two distinct cell lines, (B) cells having gone through the epithelial-to-mesenchymal transition, and (C) cells differing only by their motility. This microfluidic method may enable a fast screening and identification of invasive cells, e.g., metastatic cancer cells, even in the absence of biomarkers, thus providing a rapid diagnostics and assessment protocol for effective personalized cancer therapy.Remy ElbezJeff FolzAlan McLeanHernan RocaJoseph M. LabuzKenneth J. PientaShuichi TakayamaRaoul KopelmanPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 11 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Remy Elbez
Jeff Folz
Alan McLean
Hernan Roca
Joseph M. Labuz
Kenneth J. Pienta
Shuichi Takayama
Raoul Kopelman
Cell-morphodynamic phenotype classification with application to cancer metastasis using cell magnetorotation and machine-learning
description We define cell morphodynamics as the cell’s time dependent morphology. It could be called the cell’s shape shifting ability. To measure it we use a biomarker free, dynamic histology method, which is based on multiplexed Cell Magneto-Rotation and Machine Learning. We note that standard studies looking at cells immobilized on microscope slides cannot reveal their shape shifting, no more than pinned butterfly collections can reveal their flight patterns. Using cell magnetorotation, with the aid of cell embedded magnetic nanoparticles, our method allows each cell to move freely in 3 dimensions, with a rapid following of cell deformations in all 3-dimensions, so as to identify and classify a cell by its dynamic morphology. Using object recognition and machine learning algorithms, we continuously measure the real-time shape dynamics of each cell, where from we successfully resolve the inherent broad heterogeneity of the morphological phenotypes found in a given cancer cell population. In three illustrative experiments we have achieved clustering, differentiation, and identification of cells from (A) two distinct cell lines, (B) cells having gone through the epithelial-to-mesenchymal transition, and (C) cells differing only by their motility. This microfluidic method may enable a fast screening and identification of invasive cells, e.g., metastatic cancer cells, even in the absence of biomarkers, thus providing a rapid diagnostics and assessment protocol for effective personalized cancer therapy.
format article
author Remy Elbez
Jeff Folz
Alan McLean
Hernan Roca
Joseph M. Labuz
Kenneth J. Pienta
Shuichi Takayama
Raoul Kopelman
author_facet Remy Elbez
Jeff Folz
Alan McLean
Hernan Roca
Joseph M. Labuz
Kenneth J. Pienta
Shuichi Takayama
Raoul Kopelman
author_sort Remy Elbez
title Cell-morphodynamic phenotype classification with application to cancer metastasis using cell magnetorotation and machine-learning
title_short Cell-morphodynamic phenotype classification with application to cancer metastasis using cell magnetorotation and machine-learning
title_full Cell-morphodynamic phenotype classification with application to cancer metastasis using cell magnetorotation and machine-learning
title_fullStr Cell-morphodynamic phenotype classification with application to cancer metastasis using cell magnetorotation and machine-learning
title_full_unstemmed Cell-morphodynamic phenotype classification with application to cancer metastasis using cell magnetorotation and machine-learning
title_sort cell-morphodynamic phenotype classification with application to cancer metastasis using cell magnetorotation and machine-learning
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/fdb6ebe73a384d29930d6889ca7e3b22
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