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Preclinical and Clinical Evaluation of Magnetic-Activated Cell Separation Technology for CTC Isolation in Breast Cancer

Circulating tumor cell (CTC) count is an independent prognostic factor in early breast cancer. CTCs can be found in the blood of 20% of patients prior to neoadjuvant therapy. We aimed to assess the suitability of magnetic-activated cell separation (MACS) technology for isolation and cytological char...

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Autores principales: Lozar, Taja, Jesenko, Tanja, Kloboves Prevodnik, Veronika, Cemazar, Maja, Hosta, Violeta, Jericevic, Anja, Nolde, Natasa, Grasic Kuhar, Cvetka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522616/
https://www.ncbi.nlm.nih.gov/pubmed/33042837
http://dx.doi.org/10.3389/fonc.2020.554554
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author Lozar, Taja
Jesenko, Tanja
Kloboves Prevodnik, Veronika
Cemazar, Maja
Hosta, Violeta
Jericevic, Anja
Nolde, Natasa
Grasic Kuhar, Cvetka
author_facet Lozar, Taja
Jesenko, Tanja
Kloboves Prevodnik, Veronika
Cemazar, Maja
Hosta, Violeta
Jericevic, Anja
Nolde, Natasa
Grasic Kuhar, Cvetka
author_sort Lozar, Taja
collection PubMed
description Circulating tumor cell (CTC) count is an independent prognostic factor in early breast cancer. CTCs can be found in the blood of 20% of patients prior to neoadjuvant therapy. We aimed to assess the suitability of magnetic-activated cell separation (MACS) technology for isolation and cytological characterization of CTCs. In the preclinical part of the study, cell lines were spiked into buffy coat samples derived from healthy donors, and isolated using MACS. Breast cancer cells with preserved cell morphology were successfully isolated. In the clinical part, blood for CTC isolation was drawn from 44 patients with early and locally advanced breast cancer prior to neoadjuvant chemotherapy. Standard Giemsa, Papanicolaou and pancytokeratin staining was applied. 2.3% of samples contained cells that meet both the morphological and immunocytochemical criteria for CTC. In 32.6% of samples, partially degenerated pancytokeratin negative cells with morphological features of tumor cells were observed. In 65.1% of samples, CTCs were not found. In conclusion, our results demonstrate that morphologically intact tumor cells can be isolated using MACS technology. However, morphologically intact tumor cells were not detected in the clinical part of the study. At present, MACS technology does not appear suitable for use in a clinical cytopathology laboratory.
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spelling pubmed-75226162020-10-09 Preclinical and Clinical Evaluation of Magnetic-Activated Cell Separation Technology for CTC Isolation in Breast Cancer Lozar, Taja Jesenko, Tanja Kloboves Prevodnik, Veronika Cemazar, Maja Hosta, Violeta Jericevic, Anja Nolde, Natasa Grasic Kuhar, Cvetka Front Oncol Oncology Circulating tumor cell (CTC) count is an independent prognostic factor in early breast cancer. CTCs can be found in the blood of 20% of patients prior to neoadjuvant therapy. We aimed to assess the suitability of magnetic-activated cell separation (MACS) technology for isolation and cytological characterization of CTCs. In the preclinical part of the study, cell lines were spiked into buffy coat samples derived from healthy donors, and isolated using MACS. Breast cancer cells with preserved cell morphology were successfully isolated. In the clinical part, blood for CTC isolation was drawn from 44 patients with early and locally advanced breast cancer prior to neoadjuvant chemotherapy. Standard Giemsa, Papanicolaou and pancytokeratin staining was applied. 2.3% of samples contained cells that meet both the morphological and immunocytochemical criteria for CTC. In 32.6% of samples, partially degenerated pancytokeratin negative cells with morphological features of tumor cells were observed. In 65.1% of samples, CTCs were not found. In conclusion, our results demonstrate that morphologically intact tumor cells can be isolated using MACS technology. However, morphologically intact tumor cells were not detected in the clinical part of the study. At present, MACS technology does not appear suitable for use in a clinical cytopathology laboratory. Frontiers Media S.A. 2020-09-15 /pmc/articles/PMC7522616/ /pubmed/33042837 http://dx.doi.org/10.3389/fonc.2020.554554 Text en Copyright © 2020 Lozar, Jesenko, Kloboves Prevodnik, Cemazar, Hosta, Jericevic, Nolde and Grasic Kuhar. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Lozar, Taja
Jesenko, Tanja
Kloboves Prevodnik, Veronika
Cemazar, Maja
Hosta, Violeta
Jericevic, Anja
Nolde, Natasa
Grasic Kuhar, Cvetka
Preclinical and Clinical Evaluation of Magnetic-Activated Cell Separation Technology for CTC Isolation in Breast Cancer
title Preclinical and Clinical Evaluation of Magnetic-Activated Cell Separation Technology for CTC Isolation in Breast Cancer
title_full Preclinical and Clinical Evaluation of Magnetic-Activated Cell Separation Technology for CTC Isolation in Breast Cancer
title_fullStr Preclinical and Clinical Evaluation of Magnetic-Activated Cell Separation Technology for CTC Isolation in Breast Cancer
title_full_unstemmed Preclinical and Clinical Evaluation of Magnetic-Activated Cell Separation Technology for CTC Isolation in Breast Cancer
title_short Preclinical and Clinical Evaluation of Magnetic-Activated Cell Separation Technology for CTC Isolation in Breast Cancer
title_sort preclinical and clinical evaluation of magnetic-activated cell separation technology for ctc isolation in breast cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522616/
https://www.ncbi.nlm.nih.gov/pubmed/33042837
http://dx.doi.org/10.3389/fonc.2020.554554
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