Evidence map›Paper›PMID 30374140›Full record

ArticleScientific reports2018

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

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

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
3.8field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

48 citing papers in PubMed, 87 citations in OpenAlex.

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  18. Frontiers in cell and developmental biology · 2023
    Article
  19. Article
  20. Technologies for Viable Circulating Tumor Cell Isolation.International journal of molecular sciences · 2022
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 2 countries.

Alexandra SolerLaboratory of Rare Human Circulating Cells, University Medical Centre of Montpellier, EA2415, Montpellier, France.
Laure CayrefourcqLaboratory of Rare Human Circulating Cells, University Medical Centre of Montpellier, EA2415, Montpellier, France.
Thibault MazardDepartment of Medical Oncology, Cancer Institute of Montpellier, Montpellier, France.
Anna BabayanDepartment of Tumor Biology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Pierre-Jean LamyImagenome, Labosud, Montpellier, France.ORCID http://orcid.org/0000-0002-5750-159X
Said AssouIRMB, Montpellier University, INSERM U1183, University Medical Centre of Montpellier, Montpellier, France.
Eric AssenatDepartment of Medical Oncology, University Medical Centre of Montpellier, Montpellier, France.
Klaus PantelDepartment of Tumor Biology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Catherine Alix-PanabièresLaboratory of Rare Human Circulating Cells, University Medical Centre of Montpellier, EA2415, Montpellier, France. c-panabieres@chu-montpellier.fr.
Neuropsychiatrie : Recherche Epidemiologique et Clinique · FRInserm · FRUniversität Hamburg · DECentre Hospitalier Universitaire de Montpellier · FRInstitut d'Imagerie Biomédicale · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Antineoplastic AgentsChromosome AberrationsCluster AnalysisColonic NeoplasmsDNA-Binding ProteinsDNA Copy Number VariationsHumansIntercellular Signaling Peptides and ProteinsNeoplastic Cells, CirculatingProteomeTranscription FactorsTumor Cells, CulturedAntineoplastic AgentsDKK1 protein, humanDNA-Binding ProteinsIntercellular Signaling Peptides and ProteinsProteomeSMARCA1 protein, humanTranscription Factors

Identifiers

PMID30374140
PMCPMC6206091
OpenAlexW2897091357

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.