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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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
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.
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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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