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Autologous cell lines from circulating colon cancer cells captured from sequential liquid biopsies as model to study therapy-driven tumor changes

Circulating tumor cells (CTCs) are important clinical indicators for prognosis and treatment efficacy. However, CTC investigation is hampered by their low number, making the establishment of permanent CTC lines very challenging. We derived and characterized nine CTC lines using blood samples from a...

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Autores principales: Soler, Alexandra, Cayrefourcq, Laure, Mazard, Thibault, Babayan, Anna, Lamy, Pierre-Jean, Assou, Said, Assenat, Eric, Pantel, Klaus, Alix-Panabières, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206091/
https://www.ncbi.nlm.nih.gov/pubmed/30374140
http://dx.doi.org/10.1038/s41598-018-34365-z
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author Soler, Alexandra
Cayrefourcq, Laure
Mazard, Thibault
Babayan, Anna
Lamy, Pierre-Jean
Assou, Said
Assenat, Eric
Pantel, Klaus
Alix-Panabières, Catherine
author_facet Soler, Alexandra
Cayrefourcq, Laure
Mazard, Thibault
Babayan, Anna
Lamy, Pierre-Jean
Assou, Said
Assenat, Eric
Pantel, Klaus
Alix-Panabières, Catherine
author_sort Soler, Alexandra
collection PubMed
description Circulating tumor cells (CTCs) are important clinical indicators for prognosis and treatment efficacy. However, CTC investigation is hampered by their low number, making the establishment of permanent CTC lines very challenging. We derived and characterized nine CTC lines using blood samples from a patient with metastatic colorectal cancer collected before and after chemotherapy and targeted therapy, and during cancer progression. These cell lines displayed an intermediate epithelial/mesenchymal phenotype, stem-cell like characteristics, angiogenesis potential, an osteomimetic signature and the capacity to escape from the immune system. Moreover, they showed changes in mRNA and protein expression (e.g., DEFA6, ABCB1 and GAL), whereas analysis of chromosomal copy number aberrations revealed no significant variation over time. These data indicate that although CTC lines derived from sequential blood samples during therapy have common traits, treatment-resistant CTC clones with distinct phenotypic characteristics are selected over time.
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spelling pubmed-62060912018-11-01 Autologous cell lines from circulating colon cancer cells captured from sequential liquid biopsies as model to study therapy-driven tumor changes Soler, Alexandra Cayrefourcq, Laure Mazard, Thibault Babayan, Anna Lamy, Pierre-Jean Assou, Said Assenat, Eric Pantel, Klaus Alix-Panabières, Catherine Sci Rep Article Circulating tumor cells (CTCs) are important clinical indicators for prognosis and treatment efficacy. However, CTC investigation is hampered by their low number, making the establishment of permanent CTC lines very challenging. We derived and characterized nine CTC lines using blood samples from a patient with metastatic colorectal cancer collected before and after chemotherapy and targeted therapy, and during cancer progression. These cell lines displayed an intermediate epithelial/mesenchymal phenotype, stem-cell like characteristics, angiogenesis potential, an osteomimetic signature and the capacity to escape from the immune system. Moreover, they showed changes in mRNA and protein expression (e.g., DEFA6, ABCB1 and GAL), whereas analysis of chromosomal copy number aberrations revealed no significant variation over time. These data indicate that although CTC lines derived from sequential blood samples during therapy have common traits, treatment-resistant CTC clones with distinct phenotypic characteristics are selected over time. Nature Publishing Group UK 2018-10-29 /pmc/articles/PMC6206091/ /pubmed/30374140 http://dx.doi.org/10.1038/s41598-018-34365-z Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Soler, Alexandra
Cayrefourcq, Laure
Mazard, Thibault
Babayan, Anna
Lamy, Pierre-Jean
Assou, Said
Assenat, Eric
Pantel, Klaus
Alix-Panabières, Catherine
Autologous cell lines from circulating colon cancer cells captured from sequential liquid biopsies as model to study therapy-driven tumor changes
title Autologous cell lines from circulating colon cancer cells captured from sequential liquid biopsies as model to study therapy-driven tumor changes
title_full Autologous cell lines from circulating colon cancer cells captured from sequential liquid biopsies as model to study therapy-driven tumor changes
title_fullStr Autologous cell lines from circulating colon cancer cells captured from sequential liquid biopsies as model to study therapy-driven tumor changes
title_full_unstemmed Autologous cell lines from circulating colon cancer cells captured from sequential liquid biopsies as model to study therapy-driven tumor changes
title_short Autologous cell lines from circulating colon cancer cells captured from sequential liquid biopsies as model to study therapy-driven tumor changes
title_sort autologous cell lines from circulating colon cancer cells captured from sequential liquid biopsies as model to study therapy-driven tumor changes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6206091/
https://www.ncbi.nlm.nih.gov/pubmed/30374140
http://dx.doi.org/10.1038/s41598-018-34365-z
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