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Microfluidic enrichment for the single cell analysis of circulating tumor cells
Resistance to drug therapy is a major concern in cancer treatment. To probe clones resistant to chemotherapy, the current approach is to conduct pooled cell analysis. However, this can yield false negative outcomes, especially when we are analyzing a rare number of circulating tumor cells (CTCs) amo...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770429/ https://www.ncbi.nlm.nih.gov/pubmed/26924553 http://dx.doi.org/10.1038/srep22076 |
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author | Yeo, Trifanny Tan, Swee Jin Lim, Chew Leng Lau, Dawn Ping Xi Chua, Yong Wei Krisna, Sai Sakktee Iyer, Gopal Tan, Gek San Lim, Tony Kiat Hon Tan, Daniel S.W. Lim, Wan-Teck Lim, Chwee Teck |
author_facet | Yeo, Trifanny Tan, Swee Jin Lim, Chew Leng Lau, Dawn Ping Xi Chua, Yong Wei Krisna, Sai Sakktee Iyer, Gopal Tan, Gek San Lim, Tony Kiat Hon Tan, Daniel S.W. Lim, Wan-Teck Lim, Chwee Teck |
author_sort | Yeo, Trifanny |
collection | PubMed |
description | Resistance to drug therapy is a major concern in cancer treatment. To probe clones resistant to chemotherapy, the current approach is to conduct pooled cell analysis. However, this can yield false negative outcomes, especially when we are analyzing a rare number of circulating tumor cells (CTCs) among an abundance of other cell types. Here, we develop a microfluidic device that is able to perform high throughput, selective picking and isolation of single CTC to 100% purity from a larger population of other cells. This microfluidic device can effectively separate the very rare CTCs from blood samples from as few as 1 in 20,000 white blood cells. We first demonstrate isolation of pure tumor cells from a mixed population and track variations of acquired T790M mutations before and after drug treatment using a model PC9 cell line. With clinical CTC samples, we then show that the isolated single CTCs are representative of dominant EGFR mutations such as T790M and L858R found in the primary tumor. With this single cell recovery device, we can potentially implement personalized treatment not only through detecting genetic aberrations at the single cell level, but also through tracking such changes during an anticancer therapy. |
format | Online Article Text |
id | pubmed-4770429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47704292016-03-07 Microfluidic enrichment for the single cell analysis of circulating tumor cells Yeo, Trifanny Tan, Swee Jin Lim, Chew Leng Lau, Dawn Ping Xi Chua, Yong Wei Krisna, Sai Sakktee Iyer, Gopal Tan, Gek San Lim, Tony Kiat Hon Tan, Daniel S.W. Lim, Wan-Teck Lim, Chwee Teck Sci Rep Article Resistance to drug therapy is a major concern in cancer treatment. To probe clones resistant to chemotherapy, the current approach is to conduct pooled cell analysis. However, this can yield false negative outcomes, especially when we are analyzing a rare number of circulating tumor cells (CTCs) among an abundance of other cell types. Here, we develop a microfluidic device that is able to perform high throughput, selective picking and isolation of single CTC to 100% purity from a larger population of other cells. This microfluidic device can effectively separate the very rare CTCs from blood samples from as few as 1 in 20,000 white blood cells. We first demonstrate isolation of pure tumor cells from a mixed population and track variations of acquired T790M mutations before and after drug treatment using a model PC9 cell line. With clinical CTC samples, we then show that the isolated single CTCs are representative of dominant EGFR mutations such as T790M and L858R found in the primary tumor. With this single cell recovery device, we can potentially implement personalized treatment not only through detecting genetic aberrations at the single cell level, but also through tracking such changes during an anticancer therapy. Nature Publishing Group 2016-02-29 /pmc/articles/PMC4770429/ /pubmed/26924553 http://dx.doi.org/10.1038/srep22076 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Yeo, Trifanny Tan, Swee Jin Lim, Chew Leng Lau, Dawn Ping Xi Chua, Yong Wei Krisna, Sai Sakktee Iyer, Gopal Tan, Gek San Lim, Tony Kiat Hon Tan, Daniel S.W. Lim, Wan-Teck Lim, Chwee Teck Microfluidic enrichment for the single cell analysis of circulating tumor cells |
title | Microfluidic enrichment for the single cell analysis of circulating tumor cells |
title_full | Microfluidic enrichment for the single cell analysis of circulating tumor cells |
title_fullStr | Microfluidic enrichment for the single cell analysis of circulating tumor cells |
title_full_unstemmed | Microfluidic enrichment for the single cell analysis of circulating tumor cells |
title_short | Microfluidic enrichment for the single cell analysis of circulating tumor cells |
title_sort | microfluidic enrichment for the single cell analysis of circulating tumor cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770429/ https://www.ncbi.nlm.nih.gov/pubmed/26924553 http://dx.doi.org/10.1038/srep22076 |
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