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Detection of circulating tumor cells with a novel microfluidic system in malignant pleural mesothelioma
Detection of rare tumor cells circulating in the blood (CTCs) presents technical challenges. CellSearch, the only approved system for clinical use, fails to capture epithelial cell adhesion molecule‐negative CTCs such as malignant pleural mesothelioma (MPM). We have developed a novel microfluidic de...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361567/ https://www.ncbi.nlm.nih.gov/pubmed/30499156 http://dx.doi.org/10.1111/cas.13895 |
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author | Yoneda, Kazue Kuwata, Taiji Chikaishi, Yasuhiro Mori, Masataka Kanayama, Masatoshi Takenaka, Masaru Oka, Soichi Hirai, Ayako Imanishi, Naoko Kuroda, Koji Ichiki, Yoshinobu Ohnaga, Takashi Tanaka, Fumihiro |
author_facet | Yoneda, Kazue Kuwata, Taiji Chikaishi, Yasuhiro Mori, Masataka Kanayama, Masatoshi Takenaka, Masaru Oka, Soichi Hirai, Ayako Imanishi, Naoko Kuroda, Koji Ichiki, Yoshinobu Ohnaga, Takashi Tanaka, Fumihiro |
author_sort | Yoneda, Kazue |
collection | PubMed |
description | Detection of rare tumor cells circulating in the blood (CTCs) presents technical challenges. CellSearch, the only approved system for clinical use, fails to capture epithelial cell adhesion molecule‐negative CTCs such as malignant pleural mesothelioma (MPM). We have developed a novel microfluidic device (CTC‐chip) in which any Ab to capture CTCs is conjugated. The CTC‐chip was coated with an Ab against podoplanin that is abundantly expressed on MPM. Circulating tumor cell‐detection performance was evaluated in experimental models in which MPM cells were spiked in blood sampled from a healthy volunteer and in clinical samples drawn from MPM patients. The CTC‐chip showed superior CTC‐detection performance over CellSearch in experimental models (sensitivity, 63.3%‐64.5% vs 0%‐1.1%; P < .001) and in clinical samples (CTC‐positivity, 68.8% vs 6.3%; P < .001). A receiver operating characteristic (ROC) analysis showed that the CTC test provided a significant diagnostic performance in discrimination of unresectable disease from resectable disease (area under the ROC curve, 0.851; P = .003). The higher CTC count (≥2 cells/mL) was significantly associated with a poor prognosis (P = .030). The novel CTC‐chip enabled sensitive detection of CTCs, which provided significant diagnostic and prognostic information in MPM. |
format | Online Article Text |
id | pubmed-6361567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63615672019-02-14 Detection of circulating tumor cells with a novel microfluidic system in malignant pleural mesothelioma Yoneda, Kazue Kuwata, Taiji Chikaishi, Yasuhiro Mori, Masataka Kanayama, Masatoshi Takenaka, Masaru Oka, Soichi Hirai, Ayako Imanishi, Naoko Kuroda, Koji Ichiki, Yoshinobu Ohnaga, Takashi Tanaka, Fumihiro Cancer Sci Original Articles Detection of rare tumor cells circulating in the blood (CTCs) presents technical challenges. CellSearch, the only approved system for clinical use, fails to capture epithelial cell adhesion molecule‐negative CTCs such as malignant pleural mesothelioma (MPM). We have developed a novel microfluidic device (CTC‐chip) in which any Ab to capture CTCs is conjugated. The CTC‐chip was coated with an Ab against podoplanin that is abundantly expressed on MPM. Circulating tumor cell‐detection performance was evaluated in experimental models in which MPM cells were spiked in blood sampled from a healthy volunteer and in clinical samples drawn from MPM patients. The CTC‐chip showed superior CTC‐detection performance over CellSearch in experimental models (sensitivity, 63.3%‐64.5% vs 0%‐1.1%; P < .001) and in clinical samples (CTC‐positivity, 68.8% vs 6.3%; P < .001). A receiver operating characteristic (ROC) analysis showed that the CTC test provided a significant diagnostic performance in discrimination of unresectable disease from resectable disease (area under the ROC curve, 0.851; P = .003). The higher CTC count (≥2 cells/mL) was significantly associated with a poor prognosis (P = .030). The novel CTC‐chip enabled sensitive detection of CTCs, which provided significant diagnostic and prognostic information in MPM. John Wiley and Sons Inc. 2019-01-08 2019-02 /pmc/articles/PMC6361567/ /pubmed/30499156 http://dx.doi.org/10.1111/cas.13895 Text en © 2018 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Yoneda, Kazue Kuwata, Taiji Chikaishi, Yasuhiro Mori, Masataka Kanayama, Masatoshi Takenaka, Masaru Oka, Soichi Hirai, Ayako Imanishi, Naoko Kuroda, Koji Ichiki, Yoshinobu Ohnaga, Takashi Tanaka, Fumihiro Detection of circulating tumor cells with a novel microfluidic system in malignant pleural mesothelioma |
title | Detection of circulating tumor cells with a novel microfluidic system in malignant pleural mesothelioma |
title_full | Detection of circulating tumor cells with a novel microfluidic system in malignant pleural mesothelioma |
title_fullStr | Detection of circulating tumor cells with a novel microfluidic system in malignant pleural mesothelioma |
title_full_unstemmed | Detection of circulating tumor cells with a novel microfluidic system in malignant pleural mesothelioma |
title_short | Detection of circulating tumor cells with a novel microfluidic system in malignant pleural mesothelioma |
title_sort | detection of circulating tumor cells with a novel microfluidic system in malignant pleural mesothelioma |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6361567/ https://www.ncbi.nlm.nih.gov/pubmed/30499156 http://dx.doi.org/10.1111/cas.13895 |
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