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Vertical Magnetic Separation of Circulating Tumor Cells for Somatic Genomic-Alteration Analysis in Lung Cancer Patients

Efficient isolation and genetic analysis of circulating tumor cells (CTCs) from cancer patients’ blood is a critical step for clinical applications using CTCs. Here, we report a novel CTC-isolation method and subsequent genetic analysis. CTCs from the blood were complexed with magnetic beads coated...

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Autores principales: Yoo, Chang Eun, Park, Jong-Myeon, Moon, Hui-Sung, Joung, Je-Gun, Son, Dae-Soon, Jeon, Hyo-Jeong, Kim, Yeon Jeong, Han, Kyung-Yeon, Sun, Jong-Mu, Park, Keunchil, Park, Donghyun, Park, Woong-Yang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5124952/
https://www.ncbi.nlm.nih.gov/pubmed/27892470
http://dx.doi.org/10.1038/srep37392
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author Yoo, Chang Eun
Park, Jong-Myeon
Moon, Hui-Sung
Joung, Je-Gun
Son, Dae-Soon
Jeon, Hyo-Jeong
Kim, Yeon Jeong
Han, Kyung-Yeon
Sun, Jong-Mu
Park, Keunchil
Park, Donghyun
Park, Woong-Yang
author_facet Yoo, Chang Eun
Park, Jong-Myeon
Moon, Hui-Sung
Joung, Je-Gun
Son, Dae-Soon
Jeon, Hyo-Jeong
Kim, Yeon Jeong
Han, Kyung-Yeon
Sun, Jong-Mu
Park, Keunchil
Park, Donghyun
Park, Woong-Yang
author_sort Yoo, Chang Eun
collection PubMed
description Efficient isolation and genetic analysis of circulating tumor cells (CTCs) from cancer patients’ blood is a critical step for clinical applications using CTCs. Here, we report a novel CTC-isolation method and subsequent genetic analysis. CTCs from the blood were complexed with magnetic beads coated with antibodies against the epithelial cell adhesion molecule (EpCAM) and separated vertically on a density-gradient medium in a modified well-plate. The recovery rate of model CTCs was reasonable and the cell purity was enhanced dramatically when compared to those parameters obtained using a conventional magnetic isolation method. CTCs were recovered from an increased number of patient samples using our magnetic system vs. the FDA-approved CellSearch system (100% vs. 33%, respectively). In 8 of 13 cases, targeted deep sequencing analysis of CTCs revealed private point mutations present in CTCs but not in matched tumor samples and white blood cells (WBCs), which was also validated by droplet digital PCR. Copy-number alterations in CTCs were also observed in the corresponding tumor tissues for some patients. In this report, we showed that CTCs isolated by the EpCAM-based method had complex and diverse genetic features that were similar to those of tumor samples in some, but not all, cases.
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spelling pubmed-51249522016-12-08 Vertical Magnetic Separation of Circulating Tumor Cells for Somatic Genomic-Alteration Analysis in Lung Cancer Patients Yoo, Chang Eun Park, Jong-Myeon Moon, Hui-Sung Joung, Je-Gun Son, Dae-Soon Jeon, Hyo-Jeong Kim, Yeon Jeong Han, Kyung-Yeon Sun, Jong-Mu Park, Keunchil Park, Donghyun Park, Woong-Yang Sci Rep Article Efficient isolation and genetic analysis of circulating tumor cells (CTCs) from cancer patients’ blood is a critical step for clinical applications using CTCs. Here, we report a novel CTC-isolation method and subsequent genetic analysis. CTCs from the blood were complexed with magnetic beads coated with antibodies against the epithelial cell adhesion molecule (EpCAM) and separated vertically on a density-gradient medium in a modified well-plate. The recovery rate of model CTCs was reasonable and the cell purity was enhanced dramatically when compared to those parameters obtained using a conventional magnetic isolation method. CTCs were recovered from an increased number of patient samples using our magnetic system vs. the FDA-approved CellSearch system (100% vs. 33%, respectively). In 8 of 13 cases, targeted deep sequencing analysis of CTCs revealed private point mutations present in CTCs but not in matched tumor samples and white blood cells (WBCs), which was also validated by droplet digital PCR. Copy-number alterations in CTCs were also observed in the corresponding tumor tissues for some patients. In this report, we showed that CTCs isolated by the EpCAM-based method had complex and diverse genetic features that were similar to those of tumor samples in some, but not all, cases. Nature Publishing Group 2016-11-28 /pmc/articles/PMC5124952/ /pubmed/27892470 http://dx.doi.org/10.1038/srep37392 Text en Copyright © 2016, The Author(s) 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
Yoo, Chang Eun
Park, Jong-Myeon
Moon, Hui-Sung
Joung, Je-Gun
Son, Dae-Soon
Jeon, Hyo-Jeong
Kim, Yeon Jeong
Han, Kyung-Yeon
Sun, Jong-Mu
Park, Keunchil
Park, Donghyun
Park, Woong-Yang
Vertical Magnetic Separation of Circulating Tumor Cells for Somatic Genomic-Alteration Analysis in Lung Cancer Patients
title Vertical Magnetic Separation of Circulating Tumor Cells for Somatic Genomic-Alteration Analysis in Lung Cancer Patients
title_full Vertical Magnetic Separation of Circulating Tumor Cells for Somatic Genomic-Alteration Analysis in Lung Cancer Patients
title_fullStr Vertical Magnetic Separation of Circulating Tumor Cells for Somatic Genomic-Alteration Analysis in Lung Cancer Patients
title_full_unstemmed Vertical Magnetic Separation of Circulating Tumor Cells for Somatic Genomic-Alteration Analysis in Lung Cancer Patients
title_short Vertical Magnetic Separation of Circulating Tumor Cells for Somatic Genomic-Alteration Analysis in Lung Cancer Patients
title_sort vertical magnetic separation of circulating tumor cells for somatic genomic-alteration analysis in lung cancer patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5124952/
https://www.ncbi.nlm.nih.gov/pubmed/27892470
http://dx.doi.org/10.1038/srep37392
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