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Isolation of circulating tumor cells in non-small-cell-lung-cancer patients using a multi-flow microfluidic channel
Circulating tumor cells (CTCs) carry a wealth of information on primary and metastatic tumors critical for precise cancer detection, monitoring, and treatment. Numerous microfluidic platforms have been developed in the past few years to capture these rare cells in patient bloodstream for deciphering...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387977/ https://www.ncbi.nlm.nih.gov/pubmed/31057935 http://dx.doi.org/10.1038/s41378-019-0045-6 |
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author | Zhou, Jian Kulasinghe, Arutha Bogseth, Amanda O’Byrne, Ken Punyadeera, Chamindie Papautsky, Ian |
author_facet | Zhou, Jian Kulasinghe, Arutha Bogseth, Amanda O’Byrne, Ken Punyadeera, Chamindie Papautsky, Ian |
author_sort | Zhou, Jian |
collection | PubMed |
description | Circulating tumor cells (CTCs) carry a wealth of information on primary and metastatic tumors critical for precise cancer detection, monitoring, and treatment. Numerous microfluidic platforms have been developed in the past few years to capture these rare cells in patient bloodstream for deciphering the critical information needed. However, the practical need for a high-quality method of CTC isolation remains to be met. Herein, we demonstrate a novel multi-flow microfluidic device that is able to sensitively provide high purity (>87%) of separation outcome without labeling. Our device is constructed and configured based on the phenomenal effect of size-dependent inertial migration. The recovery rate of >93% has been achieved using spiked cancer cells at clinically relevant concentrations (10 cells per 5 mL and above). We have also successfully detected CTCs from 6 out of 8 non-small-cell-lung-cancer (NSCLC) patients, while none for 5 healthy control subjects. With these results, we envision our approach is a promising alternative for reliable CTC capture, and thus for facilitating the progress of extracting information from CTCs to personalize treatment strategies for solid tumor patients. |
format | Online Article Text |
id | pubmed-6387977 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63879772019-05-03 Isolation of circulating tumor cells in non-small-cell-lung-cancer patients using a multi-flow microfluidic channel Zhou, Jian Kulasinghe, Arutha Bogseth, Amanda O’Byrne, Ken Punyadeera, Chamindie Papautsky, Ian Microsyst Nanoeng Article Circulating tumor cells (CTCs) carry a wealth of information on primary and metastatic tumors critical for precise cancer detection, monitoring, and treatment. Numerous microfluidic platforms have been developed in the past few years to capture these rare cells in patient bloodstream for deciphering the critical information needed. However, the practical need for a high-quality method of CTC isolation remains to be met. Herein, we demonstrate a novel multi-flow microfluidic device that is able to sensitively provide high purity (>87%) of separation outcome without labeling. Our device is constructed and configured based on the phenomenal effect of size-dependent inertial migration. The recovery rate of >93% has been achieved using spiked cancer cells at clinically relevant concentrations (10 cells per 5 mL and above). We have also successfully detected CTCs from 6 out of 8 non-small-cell-lung-cancer (NSCLC) patients, while none for 5 healthy control subjects. With these results, we envision our approach is a promising alternative for reliable CTC capture, and thus for facilitating the progress of extracting information from CTCs to personalize treatment strategies for solid tumor patients. Nature Publishing Group UK 2019-02-25 /pmc/articles/PMC6387977/ /pubmed/31057935 http://dx.doi.org/10.1038/s41378-019-0045-6 Text en © The Author(s) 2019 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 Zhou, Jian Kulasinghe, Arutha Bogseth, Amanda O’Byrne, Ken Punyadeera, Chamindie Papautsky, Ian Isolation of circulating tumor cells in non-small-cell-lung-cancer patients using a multi-flow microfluidic channel |
title | Isolation of circulating tumor cells in non-small-cell-lung-cancer patients using a multi-flow microfluidic channel |
title_full | Isolation of circulating tumor cells in non-small-cell-lung-cancer patients using a multi-flow microfluidic channel |
title_fullStr | Isolation of circulating tumor cells in non-small-cell-lung-cancer patients using a multi-flow microfluidic channel |
title_full_unstemmed | Isolation of circulating tumor cells in non-small-cell-lung-cancer patients using a multi-flow microfluidic channel |
title_short | Isolation of circulating tumor cells in non-small-cell-lung-cancer patients using a multi-flow microfluidic channel |
title_sort | isolation of circulating tumor cells in non-small-cell-lung-cancer patients using a multi-flow microfluidic channel |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387977/ https://www.ncbi.nlm.nih.gov/pubmed/31057935 http://dx.doi.org/10.1038/s41378-019-0045-6 |
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