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A Microfluidic Chip for Detecting Cholangiocarcinoma Cells in Human Bile
Cholangiocarcinoma (CCA), a biliary tract malignancy, accounts for 20% of all liver cancers. There are several existing methods for diagnosis of CCA, though they are generally expensive, laborious, and suffer from low detection rates. Herein we first developed a means of partially purifying human bi...
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/PMC5484672/ https://www.ncbi.nlm.nih.gov/pubmed/28652576 http://dx.doi.org/10.1038/s41598-017-04056-2 |
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author | Hung, Lien-Yu Chiang, Nai-Jung Tsai, Wei-Chun Fu, Chien-Yu Wang, Yu-Chun Shan, Yan-Shen Lee, Gwo-Bin |
author_facet | Hung, Lien-Yu Chiang, Nai-Jung Tsai, Wei-Chun Fu, Chien-Yu Wang, Yu-Chun Shan, Yan-Shen Lee, Gwo-Bin |
author_sort | Hung, Lien-Yu |
collection | PubMed |
description | Cholangiocarcinoma (CCA), a biliary tract malignancy, accounts for 20% of all liver cancers. There are several existing methods for diagnosis of CCA, though they are generally expensive, laborious, and suffer from low detection rates. Herein we first developed a means of partially purifying human bile for consequent injection into a microfluidic chip. Then, the novel microfluidic system, which featured 1) a cell capture module, 2) an immunofluorescence (IF) staining module featuring two CCA-specific biomarkers, and 3) an optical detection module for visualization of antibody probes bound to these CCA marker proteins, was used to detect bile duct cancer cells within partially purified bile samples. As a proof of concept, CCA cells were successfully captured and identified from CCA cell cultures, blood samples inoculated with CCA cells, and clinical bile specimens. In 7.5 ml of bile, this system could detect >2, 0, and 1 positive cells in advanced stage patients, healthy patients, and chemotherapy-treated patients, respectively. In conclusion, our microfluidic system could be a promising tool for detection of cancer cells in bile, even at the earliest stages of CCA when cancer cells are at low densities relative to the total population of epithelial cells. |
format | Online Article Text |
id | pubmed-5484672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54846722017-06-30 A Microfluidic Chip for Detecting Cholangiocarcinoma Cells in Human Bile Hung, Lien-Yu Chiang, Nai-Jung Tsai, Wei-Chun Fu, Chien-Yu Wang, Yu-Chun Shan, Yan-Shen Lee, Gwo-Bin Sci Rep Article Cholangiocarcinoma (CCA), a biliary tract malignancy, accounts for 20% of all liver cancers. There are several existing methods for diagnosis of CCA, though they are generally expensive, laborious, and suffer from low detection rates. Herein we first developed a means of partially purifying human bile for consequent injection into a microfluidic chip. Then, the novel microfluidic system, which featured 1) a cell capture module, 2) an immunofluorescence (IF) staining module featuring two CCA-specific biomarkers, and 3) an optical detection module for visualization of antibody probes bound to these CCA marker proteins, was used to detect bile duct cancer cells within partially purified bile samples. As a proof of concept, CCA cells were successfully captured and identified from CCA cell cultures, blood samples inoculated with CCA cells, and clinical bile specimens. In 7.5 ml of bile, this system could detect >2, 0, and 1 positive cells in advanced stage patients, healthy patients, and chemotherapy-treated patients, respectively. In conclusion, our microfluidic system could be a promising tool for detection of cancer cells in bile, even at the earliest stages of CCA when cancer cells are at low densities relative to the total population of epithelial cells. Nature Publishing Group UK 2017-06-26 /pmc/articles/PMC5484672/ /pubmed/28652576 http://dx.doi.org/10.1038/s41598-017-04056-2 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 Hung, Lien-Yu Chiang, Nai-Jung Tsai, Wei-Chun Fu, Chien-Yu Wang, Yu-Chun Shan, Yan-Shen Lee, Gwo-Bin A Microfluidic Chip for Detecting Cholangiocarcinoma Cells in Human Bile |
title | A Microfluidic Chip for Detecting Cholangiocarcinoma Cells in Human Bile |
title_full | A Microfluidic Chip for Detecting Cholangiocarcinoma Cells in Human Bile |
title_fullStr | A Microfluidic Chip for Detecting Cholangiocarcinoma Cells in Human Bile |
title_full_unstemmed | A Microfluidic Chip for Detecting Cholangiocarcinoma Cells in Human Bile |
title_short | A Microfluidic Chip for Detecting Cholangiocarcinoma Cells in Human Bile |
title_sort | microfluidic chip for detecting cholangiocarcinoma cells in human bile |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5484672/ https://www.ncbi.nlm.nih.gov/pubmed/28652576 http://dx.doi.org/10.1038/s41598-017-04056-2 |
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