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Label-free enrichment of rare unconventional circulating neoplastic cells using a microfluidic dielectrophoretic sorting device

Cellular circulating biomarkers from the primary tumor such as circulating tumor cells (CTCs) and circulating hybrid cells (CHCs) have been described to harbor tumor-like phenotype and genotype. CHCs are present in higher numbers than CTCs supporting their translational potential. Methods for isolat...

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Autores principales: Montoya Mira, Jose, Sapre, Ajay A., Walker, Brett S., Alvarez, Jesus Bueno, Gustafson, Kyle T., Tu, Eugene, Fischer, Jared M., Wong, Melissa H., Esener, Sadik, Chiu, Yu-Jui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463600/
https://www.ncbi.nlm.nih.gov/pubmed/34561533
http://dx.doi.org/10.1038/s42003-021-02651-8
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author Montoya Mira, Jose
Sapre, Ajay A.
Walker, Brett S.
Alvarez, Jesus Bueno
Gustafson, Kyle T.
Tu, Eugene
Fischer, Jared M.
Wong, Melissa H.
Esener, Sadik
Chiu, Yu-Jui
author_facet Montoya Mira, Jose
Sapre, Ajay A.
Walker, Brett S.
Alvarez, Jesus Bueno
Gustafson, Kyle T.
Tu, Eugene
Fischer, Jared M.
Wong, Melissa H.
Esener, Sadik
Chiu, Yu-Jui
author_sort Montoya Mira, Jose
collection PubMed
description Cellular circulating biomarkers from the primary tumor such as circulating tumor cells (CTCs) and circulating hybrid cells (CHCs) have been described to harbor tumor-like phenotype and genotype. CHCs are present in higher numbers than CTCs supporting their translational potential. Methods for isolation of CHCs do not exist and are restricted to low-throughput, time consuming, and biased methodologies. We report the development of a label-free dielectrophoretic microfluidic platform facilitating enrichment of CHCs in a high-throughput and rapid fashion by depleting healthy peripheral blood mononuclear cells (PBMCs). We demonstrated up to 96.5% depletion of PBMCs resulting in 18.6-fold enrichment of cancer cells. In PBMCs from pancreatic adenocarcinoma patients, the platform enriched neoplastic cells identified by their KRAS mutant status using droplet digital PCR with one hour of processing. Enrichment was achieved in 75% of the clinical samples analyzed, establishing this approach as a promising way to non-invasively analyze tumor cells from patients.
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spelling pubmed-84636002021-10-22 Label-free enrichment of rare unconventional circulating neoplastic cells using a microfluidic dielectrophoretic sorting device Montoya Mira, Jose Sapre, Ajay A. Walker, Brett S. Alvarez, Jesus Bueno Gustafson, Kyle T. Tu, Eugene Fischer, Jared M. Wong, Melissa H. Esener, Sadik Chiu, Yu-Jui Commun Biol Article Cellular circulating biomarkers from the primary tumor such as circulating tumor cells (CTCs) and circulating hybrid cells (CHCs) have been described to harbor tumor-like phenotype and genotype. CHCs are present in higher numbers than CTCs supporting their translational potential. Methods for isolation of CHCs do not exist and are restricted to low-throughput, time consuming, and biased methodologies. We report the development of a label-free dielectrophoretic microfluidic platform facilitating enrichment of CHCs in a high-throughput and rapid fashion by depleting healthy peripheral blood mononuclear cells (PBMCs). We demonstrated up to 96.5% depletion of PBMCs resulting in 18.6-fold enrichment of cancer cells. In PBMCs from pancreatic adenocarcinoma patients, the platform enriched neoplastic cells identified by their KRAS mutant status using droplet digital PCR with one hour of processing. Enrichment was achieved in 75% of the clinical samples analyzed, establishing this approach as a promising way to non-invasively analyze tumor cells from patients. Nature Publishing Group UK 2021-09-24 /pmc/articles/PMC8463600/ /pubmed/34561533 http://dx.doi.org/10.1038/s42003-021-02651-8 Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Montoya Mira, Jose
Sapre, Ajay A.
Walker, Brett S.
Alvarez, Jesus Bueno
Gustafson, Kyle T.
Tu, Eugene
Fischer, Jared M.
Wong, Melissa H.
Esener, Sadik
Chiu, Yu-Jui
Label-free enrichment of rare unconventional circulating neoplastic cells using a microfluidic dielectrophoretic sorting device
title Label-free enrichment of rare unconventional circulating neoplastic cells using a microfluidic dielectrophoretic sorting device
title_full Label-free enrichment of rare unconventional circulating neoplastic cells using a microfluidic dielectrophoretic sorting device
title_fullStr Label-free enrichment of rare unconventional circulating neoplastic cells using a microfluidic dielectrophoretic sorting device
title_full_unstemmed Label-free enrichment of rare unconventional circulating neoplastic cells using a microfluidic dielectrophoretic sorting device
title_short Label-free enrichment of rare unconventional circulating neoplastic cells using a microfluidic dielectrophoretic sorting device
title_sort label-free enrichment of rare unconventional circulating neoplastic cells using a microfluidic dielectrophoretic sorting device
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8463600/
https://www.ncbi.nlm.nih.gov/pubmed/34561533
http://dx.doi.org/10.1038/s42003-021-02651-8
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