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In vitro validation of an ultra-sensitive scanning fluorescence microscope for analysis of Circulating Tumor Cells
Analysis of circulating tumor cells (CTC) holds promise of providing liquid biopsies from patients with cancer. However, current methods include enrichment procedures. We present a method (CytoTrack®), where CTC from 7.5 mL of blood is stained, analyzed and counted by a scanning fluorescence microsc...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153957/ https://www.ncbi.nlm.nih.gov/pubmed/24164622 http://dx.doi.org/10.1111/apm.12183 |
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author | Hillig, Thore Nygaard, Ann-Britt Nekiunaite, Laura Klingelhöfer, Jörg Sölétormos, György |
author_facet | Hillig, Thore Nygaard, Ann-Britt Nekiunaite, Laura Klingelhöfer, Jörg Sölétormos, György |
author_sort | Hillig, Thore |
collection | PubMed |
description | Analysis of circulating tumor cells (CTC) holds promise of providing liquid biopsies from patients with cancer. However, current methods include enrichment procedures. We present a method (CytoTrack®), where CTC from 7.5 mL of blood is stained, analyzed and counted by a scanning fluorescence microscope. The method was validated by breast cancer cells (MCF-7) spiked in blood from healthy donors. The number of cells spiked in each blood sample was exactly determined by cell sorter and performed in three series of three samples spiked with 10, 33 or 100 cells in addition with three control samples for each series. The recovery rate of 10, 33 and 100 tumor cells in a blood sample was 55%, 70% and 78%, percent coefficient of variation (CV%) for samples was 59%, 32% and 18%, respectively. None of the control samples contained CTC. In conclusion, the method has been validated to highly sensitively detect breast cancer cells in spiking experiments and should be tested on blood samples from breast cancer patients. The method could benefit from automation that could reduce the CV%, and further optimization of the procedure to increase the recovery. |
format | Online Article Text |
id | pubmed-4153957 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41539572014-09-08 In vitro validation of an ultra-sensitive scanning fluorescence microscope for analysis of Circulating Tumor Cells Hillig, Thore Nygaard, Ann-Britt Nekiunaite, Laura Klingelhöfer, Jörg Sölétormos, György APMIS Original Articles Analysis of circulating tumor cells (CTC) holds promise of providing liquid biopsies from patients with cancer. However, current methods include enrichment procedures. We present a method (CytoTrack®), where CTC from 7.5 mL of blood is stained, analyzed and counted by a scanning fluorescence microscope. The method was validated by breast cancer cells (MCF-7) spiked in blood from healthy donors. The number of cells spiked in each blood sample was exactly determined by cell sorter and performed in three series of three samples spiked with 10, 33 or 100 cells in addition with three control samples for each series. The recovery rate of 10, 33 and 100 tumor cells in a blood sample was 55%, 70% and 78%, percent coefficient of variation (CV%) for samples was 59%, 32% and 18%, respectively. None of the control samples contained CTC. In conclusion, the method has been validated to highly sensitively detect breast cancer cells in spiking experiments and should be tested on blood samples from breast cancer patients. The method could benefit from automation that could reduce the CV%, and further optimization of the procedure to increase the recovery. Blackwell Publishing Ltd 2014-06 2013-10-29 /pmc/articles/PMC4153957/ /pubmed/24164622 http://dx.doi.org/10.1111/apm.12183 Text en © 2014 The Authors. APMIS published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Hillig, Thore Nygaard, Ann-Britt Nekiunaite, Laura Klingelhöfer, Jörg Sölétormos, György In vitro validation of an ultra-sensitive scanning fluorescence microscope for analysis of Circulating Tumor Cells |
title | In vitro validation of an ultra-sensitive scanning fluorescence microscope for analysis of Circulating Tumor Cells |
title_full | In vitro validation of an ultra-sensitive scanning fluorescence microscope for analysis of Circulating Tumor Cells |
title_fullStr | In vitro validation of an ultra-sensitive scanning fluorescence microscope for analysis of Circulating Tumor Cells |
title_full_unstemmed | In vitro validation of an ultra-sensitive scanning fluorescence microscope for analysis of Circulating Tumor Cells |
title_short | In vitro validation of an ultra-sensitive scanning fluorescence microscope for analysis of Circulating Tumor Cells |
title_sort | in vitro validation of an ultra-sensitive scanning fluorescence microscope for analysis of circulating tumor cells |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4153957/ https://www.ncbi.nlm.nih.gov/pubmed/24164622 http://dx.doi.org/10.1111/apm.12183 |
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