Cargando…
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...
Autores principales: | , , , |
---|---|
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 |
_version_ | 1783347102829510656 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6089922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT ohnagatakashi highlyefficientcaptureofcancercellsexpressingegfrbymicrofluidicmethodsbasedonantigenantibodyassociation AT takeiyoshinori highlyefficientcaptureofcancercellsexpressingegfrbymicrofluidicmethodsbasedonantigenantibodyassociation AT nagatatakuya highlyefficientcaptureofcancercellsexpressingegfrbymicrofluidicmethodsbasedonantigenantibodyassociation AT shimadayutaka highlyefficientcaptureofcancercellsexpressingegfrbymicrofluidicmethodsbasedonantigenantibodyassociation |