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Ex vivo expansion of circulating tumour cells (CTCs)
Circulating tumour cells (CTCs) are a critical intermediate step in the process of cancer metastasis. The reliability of CTC isolation/purification has limited both the potential to report on metastatic progression and the development of CTCs as targets for therapeutic intervention. Here we report a...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988863/ https://www.ncbi.nlm.nih.gov/pubmed/36879003 http://dx.doi.org/10.1038/s41598-023-30733-6 |
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author | Mohamed, Bashir M. Ward, Mark P. Bates, Mark Spillane, Cathy D. Kelly, Tanya Martin, Cara Gallagher, Michael Heffernan, Sheena Norris, Lucy Kennedy, John Saadeh, Feras Abu Gleeson, Noreen Brooks, Doug A. Brooks, Robert D. Selemidis, Stavros O’Toole, Sharon O’Leary, John J. |
author_facet | Mohamed, Bashir M. Ward, Mark P. Bates, Mark Spillane, Cathy D. Kelly, Tanya Martin, Cara Gallagher, Michael Heffernan, Sheena Norris, Lucy Kennedy, John Saadeh, Feras Abu Gleeson, Noreen Brooks, Doug A. Brooks, Robert D. Selemidis, Stavros O’Toole, Sharon O’Leary, John J. |
author_sort | Mohamed, Bashir M. |
collection | PubMed |
description | Circulating tumour cells (CTCs) are a critical intermediate step in the process of cancer metastasis. The reliability of CTC isolation/purification has limited both the potential to report on metastatic progression and the development of CTCs as targets for therapeutic intervention. Here we report a new methodology, which optimises the culture conditions for CTCs using primary cancer cells as a model system. We exploited the known biology that CTCs thrive in hypoxic conditions, with their survival and proliferation being reliant on the activation of hypoxia-inducible factor 1 alpha (HIF-1α). We isolated epithelial-like and quasi-mesenchymal CTC phenotypes from the blood of a cancer patient and successfully cultured these cells for more than 8 weeks. The presence of CTC clusters was required to establish and maintain long-term cultures. This novel methodology for the long-term culture of CTCs will aid in the development of downstream applications, including CTC theranostics. |
format | Online Article Text |
id | pubmed-9988863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99888632023-03-08 Ex vivo expansion of circulating tumour cells (CTCs) Mohamed, Bashir M. Ward, Mark P. Bates, Mark Spillane, Cathy D. Kelly, Tanya Martin, Cara Gallagher, Michael Heffernan, Sheena Norris, Lucy Kennedy, John Saadeh, Feras Abu Gleeson, Noreen Brooks, Doug A. Brooks, Robert D. Selemidis, Stavros O’Toole, Sharon O’Leary, John J. Sci Rep Article Circulating tumour cells (CTCs) are a critical intermediate step in the process of cancer metastasis. The reliability of CTC isolation/purification has limited both the potential to report on metastatic progression and the development of CTCs as targets for therapeutic intervention. Here we report a new methodology, which optimises the culture conditions for CTCs using primary cancer cells as a model system. We exploited the known biology that CTCs thrive in hypoxic conditions, with their survival and proliferation being reliant on the activation of hypoxia-inducible factor 1 alpha (HIF-1α). We isolated epithelial-like and quasi-mesenchymal CTC phenotypes from the blood of a cancer patient and successfully cultured these cells for more than 8 weeks. The presence of CTC clusters was required to establish and maintain long-term cultures. This novel methodology for the long-term culture of CTCs will aid in the development of downstream applications, including CTC theranostics. Nature Publishing Group UK 2023-03-06 /pmc/articles/PMC9988863/ /pubmed/36879003 http://dx.doi.org/10.1038/s41598-023-30733-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Mohamed, Bashir M. Ward, Mark P. Bates, Mark Spillane, Cathy D. Kelly, Tanya Martin, Cara Gallagher, Michael Heffernan, Sheena Norris, Lucy Kennedy, John Saadeh, Feras Abu Gleeson, Noreen Brooks, Doug A. Brooks, Robert D. Selemidis, Stavros O’Toole, Sharon O’Leary, John J. Ex vivo expansion of circulating tumour cells (CTCs) |
title | Ex vivo expansion of circulating tumour cells (CTCs) |
title_full | Ex vivo expansion of circulating tumour cells (CTCs) |
title_fullStr | Ex vivo expansion of circulating tumour cells (CTCs) |
title_full_unstemmed | Ex vivo expansion of circulating tumour cells (CTCs) |
title_short | Ex vivo expansion of circulating tumour cells (CTCs) |
title_sort | ex vivo expansion of circulating tumour cells (ctcs) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9988863/ https://www.ncbi.nlm.nih.gov/pubmed/36879003 http://dx.doi.org/10.1038/s41598-023-30733-6 |
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