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Culture of circulating tumor cells using a microfilter device
Circulating tumor cells (CTCs) are associated with cancer metastasis and prognosis but their scarcity in whole blood prevents their use as a diagnostic tool. The purpose of the present study was to establish a novel approach to capture and cultivate CTCs using a microfilter device. The present study...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10091075/ https://www.ncbi.nlm.nih.gov/pubmed/36999627 http://dx.doi.org/10.3892/or.2023.8538 |
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author | Furukawa, Atsuko Mori, Tomoko Shimomura, Osamu Araki, Kazuhisa Oda, Tatsuya Matsusaka, Satoshi |
author_facet | Furukawa, Atsuko Mori, Tomoko Shimomura, Osamu Araki, Kazuhisa Oda, Tatsuya Matsusaka, Satoshi |
author_sort | Furukawa, Atsuko |
collection | PubMed |
description | Circulating tumor cells (CTCs) are associated with cancer metastasis and prognosis but their scarcity in whole blood prevents their use as a diagnostic tool. The purpose of the present study was to establish a novel approach to capture and cultivate CTCs using a microfilter device. The present study was a prospective study of patients with pancreatic cancer at the University of Tsukuba Hospital (Tsukuba, Japan). From each patient, 5 ml of whole blood was collected into an EDTA collection tube. Whole blood was filtered to isolate CTCs and cells captured on the microfilter were cultured in place. A total of 15 patients were enrolled. CTCs and/or CTC clusters were detected in 2 of 6 cases on day 0. In all cases, CTCs and/or formed clusters and/or colonies were observed during long-term culture periods of up to 103 days. In samples where CTCs were not immediately evident, CTC clusters and colonies emerged after long-term culture. To confirm activity of the cultured CTCs on the filters, staining with Calcein AM was performed and epithelial cellular adhesion molecule-positive cells were observed. The system enables the capture and culture of CTCs. Cultured CTCs may be used for patient-specific drug susceptibility testing and genomic profiling of cancer. |
format | Online Article Text |
id | pubmed-10091075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-100910752023-04-13 Culture of circulating tumor cells using a microfilter device Furukawa, Atsuko Mori, Tomoko Shimomura, Osamu Araki, Kazuhisa Oda, Tatsuya Matsusaka, Satoshi Oncol Rep Articles Circulating tumor cells (CTCs) are associated with cancer metastasis and prognosis but their scarcity in whole blood prevents their use as a diagnostic tool. The purpose of the present study was to establish a novel approach to capture and cultivate CTCs using a microfilter device. The present study was a prospective study of patients with pancreatic cancer at the University of Tsukuba Hospital (Tsukuba, Japan). From each patient, 5 ml of whole blood was collected into an EDTA collection tube. Whole blood was filtered to isolate CTCs and cells captured on the microfilter were cultured in place. A total of 15 patients were enrolled. CTCs and/or CTC clusters were detected in 2 of 6 cases on day 0. In all cases, CTCs and/or formed clusters and/or colonies were observed during long-term culture periods of up to 103 days. In samples where CTCs were not immediately evident, CTC clusters and colonies emerged after long-term culture. To confirm activity of the cultured CTCs on the filters, staining with Calcein AM was performed and epithelial cellular adhesion molecule-positive cells were observed. The system enables the capture and culture of CTCs. Cultured CTCs may be used for patient-specific drug susceptibility testing and genomic profiling of cancer. D.A. Spandidos 2023-03-31 /pmc/articles/PMC10091075/ /pubmed/36999627 http://dx.doi.org/10.3892/or.2023.8538 Text en Copyright: © Furukawa et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , 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 | Articles Furukawa, Atsuko Mori, Tomoko Shimomura, Osamu Araki, Kazuhisa Oda, Tatsuya Matsusaka, Satoshi Culture of circulating tumor cells using a microfilter device |
title | Culture of circulating tumor cells using a microfilter device |
title_full | Culture of circulating tumor cells using a microfilter device |
title_fullStr | Culture of circulating tumor cells using a microfilter device |
title_full_unstemmed | Culture of circulating tumor cells using a microfilter device |
title_short | Culture of circulating tumor cells using a microfilter device |
title_sort | culture of circulating tumor cells using a microfilter device |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10091075/ https://www.ncbi.nlm.nih.gov/pubmed/36999627 http://dx.doi.org/10.3892/or.2023.8538 |
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