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Highly efficient capture of cancer cells expressing EGFR by microfluidic methods based on antigen-antibody association

Epidermal growth factor receptor (EGFR) was evaluated as a target antigen for cancer cell capture by microfluidic methods based on antigen-antibody association. A polymer CTC-chip microfluidic device was surface-functionalized with three different anti-EGFR antibodies and used to capture EGFR-expres...

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Autores principales: Ohnaga, Takashi, Takei, Yoshinori, Nagata, Takuya, Shimada, Yutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089922/
https://www.ncbi.nlm.nih.gov/pubmed/30104638
http://dx.doi.org/10.1038/s41598-018-30511-9
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author Ohnaga, Takashi
Takei, Yoshinori
Nagata, Takuya
Shimada, Yutaka
author_facet Ohnaga, Takashi
Takei, Yoshinori
Nagata, Takuya
Shimada, Yutaka
author_sort Ohnaga, Takashi
collection PubMed
description Epidermal growth factor receptor (EGFR) was evaluated as a target antigen for cancer cell capture by microfluidic methods based on antigen-antibody association. A polymer CTC-chip microfluidic device was surface-functionalized with three different anti-EGFR antibodies and used to capture EGFR-expressing cancer cells. Capture efficacy depended on the type of antibody used, and cetuximab efficiently captured cancer cell lines that had a wide range of EGFR expression. Capture efficiency was analyzed from the viewpoint of antigen-antibody association in a kinetic process, i.e., cell rolling well-known in leukocyte adhesion, and antibodies with a smaller dissociation constant were shown to result in more efficient capture. Moreover, a lower limit of cellular EGFR expression level for the capture was estimated and methods to decrease the limit were discussed based on densities of anti-EGFR antibody on the device surface.
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spelling pubmed-60899222018-08-17 Highly efficient capture of cancer cells expressing EGFR by microfluidic methods based on antigen-antibody association Ohnaga, Takashi Takei, Yoshinori Nagata, Takuya Shimada, Yutaka Sci Rep Article Epidermal growth factor receptor (EGFR) was evaluated as a target antigen for cancer cell capture by microfluidic methods based on antigen-antibody association. A polymer CTC-chip microfluidic device was surface-functionalized with three different anti-EGFR antibodies and used to capture EGFR-expressing cancer cells. Capture efficacy depended on the type of antibody used, and cetuximab efficiently captured cancer cell lines that had a wide range of EGFR expression. Capture efficiency was analyzed from the viewpoint of antigen-antibody association in a kinetic process, i.e., cell rolling well-known in leukocyte adhesion, and antibodies with a smaller dissociation constant were shown to result in more efficient capture. Moreover, a lower limit of cellular EGFR expression level for the capture was estimated and methods to decrease the limit were discussed based on densities of anti-EGFR antibody on the device surface. Nature Publishing Group UK 2018-08-13 /pmc/articles/PMC6089922/ /pubmed/30104638 http://dx.doi.org/10.1038/s41598-018-30511-9 Text en © The Author(s) 2018 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
Ohnaga, Takashi
Takei, Yoshinori
Nagata, Takuya
Shimada, Yutaka
Highly efficient capture of cancer cells expressing EGFR by microfluidic methods based on antigen-antibody association
title Highly efficient capture of cancer cells expressing EGFR by microfluidic methods based on antigen-antibody association
title_full Highly efficient capture of cancer cells expressing EGFR by microfluidic methods based on antigen-antibody association
title_fullStr Highly efficient capture of cancer cells expressing EGFR by microfluidic methods based on antigen-antibody association
title_full_unstemmed Highly efficient capture of cancer cells expressing EGFR by microfluidic methods based on antigen-antibody association
title_short Highly efficient capture of cancer cells expressing EGFR by microfluidic methods based on antigen-antibody association
title_sort highly efficient capture of cancer cells expressing egfr by microfluidic methods based on antigen-antibody association
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089922/
https://www.ncbi.nlm.nih.gov/pubmed/30104638
http://dx.doi.org/10.1038/s41598-018-30511-9
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