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Ultra-fast vitrification of patient-derived circulating tumor cell lines
Emerging technologies have enabled the isolation and characterization of rare circulating tumor cells (CTCs) from the blood of metastatic cancer patients. CTCs represent a non-invasive opportunity to gain information regarding the primary tumor and recent reports suggest CTCs have value as an indica...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5825040/ https://www.ncbi.nlm.nih.gov/pubmed/29474365 http://dx.doi.org/10.1371/journal.pone.0192734 |
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author | Sandlin, Rebecca D. Wong, Keith H. K. Tessier, Shannon N. Swei, Anisa Bookstaver, Lauren D. Ahearn, Bennett E. Maheswaran, Shyamala Haber, Daniel A. Stott, Shannon L. Toner, Mehmet |
author_facet | Sandlin, Rebecca D. Wong, Keith H. K. Tessier, Shannon N. Swei, Anisa Bookstaver, Lauren D. Ahearn, Bennett E. Maheswaran, Shyamala Haber, Daniel A. Stott, Shannon L. Toner, Mehmet |
author_sort | Sandlin, Rebecca D. |
collection | PubMed |
description | Emerging technologies have enabled the isolation and characterization of rare circulating tumor cells (CTCs) from the blood of metastatic cancer patients. CTCs represent a non-invasive opportunity to gain information regarding the primary tumor and recent reports suggest CTCs have value as an indicator of disease status. CTCs are fragile and difficult to expand in vitro, so typically molecular characterization must be performed immediately following isolation. To ease experimental timelines and enable biobanking, cryopreservation methods are needed. However, extensive cellular heterogeneity and the rarity of CTCs complicates the optimization of cryopreservation methods based upon cell type, necessitating a standardized protocol. Here, we optimized a previously reported vitrification protocol to preserve patient-derived CTC cell lines using highly conductive silica microcapillaries to achieve ultra-fast cooling rates with low cryoprotectant concentrations. Using this vitrification protocol, five CTC cell lines were cooled to cryogenic temperatures. Thawed CTCs exhibited high cell viability and expanded under in vitro cell culture conditions. EpCAM biomarker expression was maintained for each CTC cell line. One CTC cell line was selected for molecular characterization, revealing that RNA integrity was maintained after storage. A qPCR panel showed no significant difference in thawed CTCs compared to fresh controls. The data presented here suggests vitrification may enable the standardization of cryopreservation methods for CTCs. |
format | Online Article Text |
id | pubmed-5825040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58250402018-03-19 Ultra-fast vitrification of patient-derived circulating tumor cell lines Sandlin, Rebecca D. Wong, Keith H. K. Tessier, Shannon N. Swei, Anisa Bookstaver, Lauren D. Ahearn, Bennett E. Maheswaran, Shyamala Haber, Daniel A. Stott, Shannon L. Toner, Mehmet PLoS One Research Article Emerging technologies have enabled the isolation and characterization of rare circulating tumor cells (CTCs) from the blood of metastatic cancer patients. CTCs represent a non-invasive opportunity to gain information regarding the primary tumor and recent reports suggest CTCs have value as an indicator of disease status. CTCs are fragile and difficult to expand in vitro, so typically molecular characterization must be performed immediately following isolation. To ease experimental timelines and enable biobanking, cryopreservation methods are needed. However, extensive cellular heterogeneity and the rarity of CTCs complicates the optimization of cryopreservation methods based upon cell type, necessitating a standardized protocol. Here, we optimized a previously reported vitrification protocol to preserve patient-derived CTC cell lines using highly conductive silica microcapillaries to achieve ultra-fast cooling rates with low cryoprotectant concentrations. Using this vitrification protocol, five CTC cell lines were cooled to cryogenic temperatures. Thawed CTCs exhibited high cell viability and expanded under in vitro cell culture conditions. EpCAM biomarker expression was maintained for each CTC cell line. One CTC cell line was selected for molecular characterization, revealing that RNA integrity was maintained after storage. A qPCR panel showed no significant difference in thawed CTCs compared to fresh controls. The data presented here suggests vitrification may enable the standardization of cryopreservation methods for CTCs. Public Library of Science 2018-02-23 /pmc/articles/PMC5825040/ /pubmed/29474365 http://dx.doi.org/10.1371/journal.pone.0192734 Text en © 2018 Sandlin et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Sandlin, Rebecca D. Wong, Keith H. K. Tessier, Shannon N. Swei, Anisa Bookstaver, Lauren D. Ahearn, Bennett E. Maheswaran, Shyamala Haber, Daniel A. Stott, Shannon L. Toner, Mehmet Ultra-fast vitrification of patient-derived circulating tumor cell lines |
title | Ultra-fast vitrification of patient-derived circulating tumor cell lines |
title_full | Ultra-fast vitrification of patient-derived circulating tumor cell lines |
title_fullStr | Ultra-fast vitrification of patient-derived circulating tumor cell lines |
title_full_unstemmed | Ultra-fast vitrification of patient-derived circulating tumor cell lines |
title_short | Ultra-fast vitrification of patient-derived circulating tumor cell lines |
title_sort | ultra-fast vitrification of patient-derived circulating tumor cell lines |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5825040/ https://www.ncbi.nlm.nih.gov/pubmed/29474365 http://dx.doi.org/10.1371/journal.pone.0192734 |
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