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

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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. / Soler, Alexandra; Cayrefourcq, Laure; Mazard, Thibault; Babayan, Anna; Lamy, Pierre-Jean; Assou, Said; Assenat, Eric; Pantel, Klaus; Alix-Panabières, Catherine.

In: SCI REP-UK, Vol. 8, No. 1, 29.10.2018, p. 15931.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

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Soler, A, Cayrefourcq, L, Mazard, T, Babayan, A, Lamy, P-J, Assou, S, Assenat, E, Pantel, K & Alix-Panabières, C 2018, 'Autologous cell lines from circulating colon cancer cells captured from sequential liquid biopsies as model to study therapy-driven tumor changes', SCI REP-UK, vol. 8, no. 1, pp. 15931. https://doi.org/10.1038/s41598-018-34365-z

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Bibtex

@article{2f002f6233bd43d89fb1252d73142496,
title = "Autologous cell lines from circulating colon cancer cells captured from sequential liquid biopsies as model to study therapy-driven tumor changes",
abstract = "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.",
keywords = "Journal Article",
author = "Alexandra Soler and Laure Cayrefourcq and Thibault Mazard and Anna Babayan and Pierre-Jean Lamy and Said Assou and Eric Assenat and Klaus Pantel and Catherine Alix-Panabi{\`e}res",
year = "2018",
month = oct,
day = "29",
doi = "10.1038/s41598-018-34365-z",
language = "English",
volume = "8",
pages = "15931",
journal = "SCI REP-UK",
issn = "2045-2322",
publisher = "NATURE PUBLISHING GROUP",
number = "1",

}

RIS

TY - JOUR

T1 - Autologous cell lines from circulating colon cancer cells captured from sequential liquid biopsies as model to study therapy-driven tumor changes

AU - Soler, Alexandra

AU - Cayrefourcq, Laure

AU - Mazard, Thibault

AU - Babayan, Anna

AU - Lamy, Pierre-Jean

AU - Assou, Said

AU - Assenat, Eric

AU - Pantel, Klaus

AU - Alix-Panabières, Catherine

PY - 2018/10/29

Y1 - 2018/10/29

N2 - 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.

AB - 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.

KW - Journal Article

U2 - 10.1038/s41598-018-34365-z

DO - 10.1038/s41598-018-34365-z

M3 - SCORING: Journal article

C2 - 30374140

VL - 8

SP - 15931

JO - SCI REP-UK

JF - SCI REP-UK

SN - 2045-2322

IS - 1

ER -