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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.
Afiliação
  • Soler A; Laboratory of Rare Human Circulating Cells, University Medical Centre of Montpellier, EA2415, Montpellier, France.
  • Cayrefourcq L; Laboratory of Rare Human Circulating Cells, University Medical Centre of Montpellier, EA2415, Montpellier, France.
  • Mazard T; Department of Medical Oncology, Cancer Institute of Montpellier, Montpellier, France.
  • Babayan A; Department of Tumor Biology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Lamy PJ; Imagenome, Labosud, Montpellier, France.
  • Assou S; IRMB, Montpellier University, INSERM U1183, University Medical Centre of Montpellier, Montpellier, France.
  • Assenat E; Department of Medical Oncology, University Medical Centre of Montpellier, Montpellier, France.
  • Pantel K; Department of Tumor Biology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
  • Alix-Panabières C; Laboratory of Rare Human Circulating Cells, University Medical Centre of Montpellier, EA2415, Montpellier, France. c-panabieres@chu-montpellier.fr.
Sci Rep ; 8(1): 15931, 2018 10 29.
Article em En | MEDLINE | ID: mdl-30374140
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article