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Highly-sensitive capture of circulating tumor cells using micro-ellipse filters
Circulating tumor cells (CTCs) detection, enumeration and characterization with microfluidic chips has critical significance in cancer prognosis offering a non-invasive “liquid biopsy”. Based on physical differences of size and deformability, we explore micro-ellipse filters consisting of microfuidi...
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/PMC5428045/ https://www.ncbi.nlm.nih.gov/pubmed/28377598 http://dx.doi.org/10.1038/s41598-017-00232-6 |
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author | Chen, Hongmei Cao, Baoshan Sun, Bo Cao, Yapeng Yang, Ke Lin, Yu-Sheng |
author_facet | Chen, Hongmei Cao, Baoshan Sun, Bo Cao, Yapeng Yang, Ke Lin, Yu-Sheng |
author_sort | Chen, Hongmei |
collection | PubMed |
description | Circulating tumor cells (CTCs) detection, enumeration and characterization with microfluidic chips has critical significance in cancer prognosis offering a non-invasive “liquid biopsy”. Based on physical differences of size and deformability, we explore micro-ellipse filters consisting of microfuidic slits in series gradually narrowed. Slender tunnels sensitively capture tumor cells with slim chance to escape. Tumor cells could reside at capture sites organized by arrays of micro-ellipse microposts enduring less stress. Circular elliptical microstructures produce smooth flow minimally reducing any damage. “Air Suction” could extremely shorten capture. Capture efficiency comes out to be a robust yield of 90% and percentage obeys Gaussian distribution at various stages. With rare number accurately enumerated, micro-Ellipse filters have been tested high efficiently capturing tumor cells in both whole and lysed blood. To clinically validate the device, the microfluidic chip was utilized to identify and capture CTCs from metastatic breast, colon and non-small-cell lung (NSCLC) cancer patients. CTCs were detected positive in all samples with 4 patients having more than 20 CTCs. Those sensitive results are consistent with theoretical expectation. Efficient micro-ellipse filters enable clinical enumeration of metastasis, on-chip anti-cancer drug responses and biological molecular analysis. |
format | Online Article Text |
id | pubmed-5428045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54280452017-05-15 Highly-sensitive capture of circulating tumor cells using micro-ellipse filters Chen, Hongmei Cao, Baoshan Sun, Bo Cao, Yapeng Yang, Ke Lin, Yu-Sheng Sci Rep Article Circulating tumor cells (CTCs) detection, enumeration and characterization with microfluidic chips has critical significance in cancer prognosis offering a non-invasive “liquid biopsy”. Based on physical differences of size and deformability, we explore micro-ellipse filters consisting of microfuidic slits in series gradually narrowed. Slender tunnels sensitively capture tumor cells with slim chance to escape. Tumor cells could reside at capture sites organized by arrays of micro-ellipse microposts enduring less stress. Circular elliptical microstructures produce smooth flow minimally reducing any damage. “Air Suction” could extremely shorten capture. Capture efficiency comes out to be a robust yield of 90% and percentage obeys Gaussian distribution at various stages. With rare number accurately enumerated, micro-Ellipse filters have been tested high efficiently capturing tumor cells in both whole and lysed blood. To clinically validate the device, the microfluidic chip was utilized to identify and capture CTCs from metastatic breast, colon and non-small-cell lung (NSCLC) cancer patients. CTCs were detected positive in all samples with 4 patients having more than 20 CTCs. Those sensitive results are consistent with theoretical expectation. Efficient micro-ellipse filters enable clinical enumeration of metastasis, on-chip anti-cancer drug responses and biological molecular analysis. Nature Publishing Group UK 2017-04-04 /pmc/articles/PMC5428045/ /pubmed/28377598 http://dx.doi.org/10.1038/s41598-017-00232-6 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 Chen, Hongmei Cao, Baoshan Sun, Bo Cao, Yapeng Yang, Ke Lin, Yu-Sheng Highly-sensitive capture of circulating tumor cells using micro-ellipse filters |
title | Highly-sensitive capture of circulating tumor cells using micro-ellipse filters |
title_full | Highly-sensitive capture of circulating tumor cells using micro-ellipse filters |
title_fullStr | Highly-sensitive capture of circulating tumor cells using micro-ellipse filters |
title_full_unstemmed | Highly-sensitive capture of circulating tumor cells using micro-ellipse filters |
title_short | Highly-sensitive capture of circulating tumor cells using micro-ellipse filters |
title_sort | highly-sensitive capture of circulating tumor cells using micro-ellipse filters |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428045/ https://www.ncbi.nlm.nih.gov/pubmed/28377598 http://dx.doi.org/10.1038/s41598-017-00232-6 |
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