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The detection of EpCAM(+) and EpCAM(–) circulating tumor cells
EpCAM expressing circulating tumor cells, detected by CellSearch, are predictive of short survival in several cancers and may serve as a liquid biopsy to guide therapy. Here we investigate the presence of EpCAM(+) CTC detected by CellSearch and EpCAM(–) CTC discarded by CellSearch, after EpCAM based...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4505332/ https://www.ncbi.nlm.nih.gov/pubmed/26184843 http://dx.doi.org/10.1038/srep12270 |
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author | Wit, Sanne de Dalum, Guus van Lenferink, Aufried T. M. Tibbe, Arjan G. J. Hiltermann, T. Jeroen N. Groen, Harry J. M. van Rijn, Cees J. M. Terstappen, Leon W. M. M. |
author_facet | Wit, Sanne de Dalum, Guus van Lenferink, Aufried T. M. Tibbe, Arjan G. J. Hiltermann, T. Jeroen N. Groen, Harry J. M. van Rijn, Cees J. M. Terstappen, Leon W. M. M. |
author_sort | Wit, Sanne de |
collection | PubMed |
description | EpCAM expressing circulating tumor cells, detected by CellSearch, are predictive of short survival in several cancers and may serve as a liquid biopsy to guide therapy. Here we investigate the presence of EpCAM(+) CTC detected by CellSearch and EpCAM(–) CTC discarded by CellSearch, after EpCAM based enrichment. EpCAM(–) CTC were identified by filtration and fluorescent labelling. This approach was validated using different cell lines spiked into blood and evaluated on blood samples of 27 metastatic lung cancer patients. The majority of spiked EpCAM(+) cells could be detected with CellSearch, whereas most spiked cells with EpCAM(low) or EpCAM(–) expression were detected using filtration. Five or more CTC were detected in 15% of the patient samples, this increased to 41% when adding the CTC detected in the discarded blood. The number of patients with CTC and the number of CTC detected were doubled by the presence of EpCAM(–) CTC. In this pilot study, the presence of EpCAM(+) CTC was associated with poor outcome, whereas the EpCAM(–) CTC were not. This observation will need to be confirmed in larger studies and molecular characterization needs to be conducted to elucidate differences between EpCAM(–) and EpCAM(+) CTC. |
format | Online Article Text |
id | pubmed-4505332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45053322015-07-23 The detection of EpCAM(+) and EpCAM(–) circulating tumor cells Wit, Sanne de Dalum, Guus van Lenferink, Aufried T. M. Tibbe, Arjan G. J. Hiltermann, T. Jeroen N. Groen, Harry J. M. van Rijn, Cees J. M. Terstappen, Leon W. M. M. Sci Rep Article EpCAM expressing circulating tumor cells, detected by CellSearch, are predictive of short survival in several cancers and may serve as a liquid biopsy to guide therapy. Here we investigate the presence of EpCAM(+) CTC detected by CellSearch and EpCAM(–) CTC discarded by CellSearch, after EpCAM based enrichment. EpCAM(–) CTC were identified by filtration and fluorescent labelling. This approach was validated using different cell lines spiked into blood and evaluated on blood samples of 27 metastatic lung cancer patients. The majority of spiked EpCAM(+) cells could be detected with CellSearch, whereas most spiked cells with EpCAM(low) or EpCAM(–) expression were detected using filtration. Five or more CTC were detected in 15% of the patient samples, this increased to 41% when adding the CTC detected in the discarded blood. The number of patients with CTC and the number of CTC detected were doubled by the presence of EpCAM(–) CTC. In this pilot study, the presence of EpCAM(+) CTC was associated with poor outcome, whereas the EpCAM(–) CTC were not. This observation will need to be confirmed in larger studies and molecular characterization needs to be conducted to elucidate differences between EpCAM(–) and EpCAM(+) CTC. Nature Publishing Group 2015-07-17 /pmc/articles/PMC4505332/ /pubmed/26184843 http://dx.doi.org/10.1038/srep12270 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wit, Sanne de Dalum, Guus van Lenferink, Aufried T. M. Tibbe, Arjan G. J. Hiltermann, T. Jeroen N. Groen, Harry J. M. van Rijn, Cees J. M. Terstappen, Leon W. M. M. The detection of EpCAM(+) and EpCAM(–) circulating tumor cells |
title | The detection of EpCAM(+) and EpCAM(–) circulating tumor cells |
title_full | The detection of EpCAM(+) and EpCAM(–) circulating tumor cells |
title_fullStr | The detection of EpCAM(+) and EpCAM(–) circulating tumor cells |
title_full_unstemmed | The detection of EpCAM(+) and EpCAM(–) circulating tumor cells |
title_short | The detection of EpCAM(+) and EpCAM(–) circulating tumor cells |
title_sort | detection of epcam(+) and epcam(–) circulating tumor cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4505332/ https://www.ncbi.nlm.nih.gov/pubmed/26184843 http://dx.doi.org/10.1038/srep12270 |
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