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Microfluidic Isolation of Circulating Tumor Cell Clusters by Size and Asymmetry
Circulating tumor cell clusters (CTC clusters) are potent initiators of metastasis and potentially useful clinical markers for patients with cancer. Although there are numerous devices developed to isolate individual circulating tumor cells from blood, these devices are ineffective at capturing CTC...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446400/ https://www.ncbi.nlm.nih.gov/pubmed/28550299 http://dx.doi.org/10.1038/s41598-017-01150-3 |
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author | Au, Sam H. Edd, Jon Stoddard, Amy E. Wong, Keith H. K. Fachin, Fabio Maheswaran, Shyamala Haber, Daniel A. Stott, Shannon L. Kapur, Ravi Toner, Mehmet |
author_facet | Au, Sam H. Edd, Jon Stoddard, Amy E. Wong, Keith H. K. Fachin, Fabio Maheswaran, Shyamala Haber, Daniel A. Stott, Shannon L. Kapur, Ravi Toner, Mehmet |
author_sort | Au, Sam H. |
collection | PubMed |
description | Circulating tumor cell clusters (CTC clusters) are potent initiators of metastasis and potentially useful clinical markers for patients with cancer. Although there are numerous devices developed to isolate individual circulating tumor cells from blood, these devices are ineffective at capturing CTC clusters, incapable of separating clusters from single cells and/or cause cluster damage or dissociation during processing. The only device currently able to specifically isolate CTC clusters from single CTCs and blood cells relies on the batch immobilization of clusters onto micropillars which necessitates long residence times and causes damage to clusters during release. Here, we present a two-stage continuous microfluidic chip that isolates and recovers viable CTC clusters from blood. This approach uses deterministic lateral displacement to sort clusters by capitalizing on two geometric properties: size and asymmetry. Cultured breast cancer CTC clusters containing between 2–100 + cells were recovered from whole blood using this integrated two-stage device with minimal cluster dissociation, 99% recovery of large clusters, cell viabilities over 87% and greater than five-log depletion of red blood cells. This continuous-flow cluster chip will enable further studies examining CTC clusters in research and clinical applications. |
format | Online Article Text |
id | pubmed-5446400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54464002017-05-30 Microfluidic Isolation of Circulating Tumor Cell Clusters by Size and Asymmetry Au, Sam H. Edd, Jon Stoddard, Amy E. Wong, Keith H. K. Fachin, Fabio Maheswaran, Shyamala Haber, Daniel A. Stott, Shannon L. Kapur, Ravi Toner, Mehmet Sci Rep Article Circulating tumor cell clusters (CTC clusters) are potent initiators of metastasis and potentially useful clinical markers for patients with cancer. Although there are numerous devices developed to isolate individual circulating tumor cells from blood, these devices are ineffective at capturing CTC clusters, incapable of separating clusters from single cells and/or cause cluster damage or dissociation during processing. The only device currently able to specifically isolate CTC clusters from single CTCs and blood cells relies on the batch immobilization of clusters onto micropillars which necessitates long residence times and causes damage to clusters during release. Here, we present a two-stage continuous microfluidic chip that isolates and recovers viable CTC clusters from blood. This approach uses deterministic lateral displacement to sort clusters by capitalizing on two geometric properties: size and asymmetry. Cultured breast cancer CTC clusters containing between 2–100 + cells were recovered from whole blood using this integrated two-stage device with minimal cluster dissociation, 99% recovery of large clusters, cell viabilities over 87% and greater than five-log depletion of red blood cells. This continuous-flow cluster chip will enable further studies examining CTC clusters in research and clinical applications. Nature Publishing Group UK 2017-05-26 /pmc/articles/PMC5446400/ /pubmed/28550299 http://dx.doi.org/10.1038/s41598-017-01150-3 Text en © The Author(s) 2017 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/. |
spellingShingle | Article Au, Sam H. Edd, Jon Stoddard, Amy E. Wong, Keith H. K. Fachin, Fabio Maheswaran, Shyamala Haber, Daniel A. Stott, Shannon L. Kapur, Ravi Toner, Mehmet Microfluidic Isolation of Circulating Tumor Cell Clusters by Size and Asymmetry |
title | Microfluidic Isolation of Circulating Tumor Cell Clusters by Size and Asymmetry |
title_full | Microfluidic Isolation of Circulating Tumor Cell Clusters by Size and Asymmetry |
title_fullStr | Microfluidic Isolation of Circulating Tumor Cell Clusters by Size and Asymmetry |
title_full_unstemmed | Microfluidic Isolation of Circulating Tumor Cell Clusters by Size and Asymmetry |
title_short | Microfluidic Isolation of Circulating Tumor Cell Clusters by Size and Asymmetry |
title_sort | microfluidic isolation of circulating tumor cell clusters by size and asymmetry |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446400/ https://www.ncbi.nlm.nih.gov/pubmed/28550299 http://dx.doi.org/10.1038/s41598-017-01150-3 |
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