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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
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.
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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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