Evidence map›Paper›PMID 27456153›Full record

ArticleGut2017

Circulating tumour cells from patients with colorectal cancer have cancer stem cell hallmarks in

Fanny Grillet, Elsa Bayet, Olivia Villeronce, Luke Zappia, Ebba Louise Lagerqvist, Sebastian Lunke, Emmanuelle Charafe-Jauffret, Kym Pham, Christina Molck, Nathalie Rolland and 11 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Gut, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01577511 (Invasiveness and Chemoresistance of Cancer Stem Cells in Colon Cancer), which is not on this map. Cited by 132 papers.

0numbers the graph read from it
0cells of the map it votes in
132citing papers in PubMed
9.5field-weighted citation impact, top 1% 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.

NCT01577511 completednot on this map

Invasiveness and Chemoresistance of Cancer Stem Cells in Colon Cancer: Molecular Characterization and Implications for Therapeutic Strategies

TypeobservationalSponsorCentre Hospitalier Universitaire de NīmesRan2012 to 2016Enrolled60ConditionsColorectal NeoplasmsArmsSamples and follow up
3 · Its place in the literature

Who cites it

132 citing papers in PubMed, 203 citations in OpenAlex.

  1. Review
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  5. Article
  6. Article
  7. Review
  8. Review
  9. The Need for a Systems Biology Approach in Cancer Explained.International journal of molecular sciences · 2025
    Review
  10. Review
  11. Progastrin Promotes Colorectal Cancer Stem Cell-Like Properties via the Receptor PZR.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  12. EMT and cancer: what clinicians should know.Nature reviews. Clinical oncology · 2025
    Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Precision Oncology Framework Using Circulating Tumor Cells.International journal of molecular sciences · 2025
    Review
  18. Article
  19. Review
  20. Review

72 more citing papers are in PubMed but not listed here.

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

21 authors at 9 institutions in 5 countries.

Fanny GrilletCentre National de la Recherche Scientifique, UMR5203, Institut de Génomique Fonctionnelle, Montpellier, France.
Elsa BayetCentre National de la Recherche Scientifique, UMR5203, Institut de Génomique Fonctionnelle, Montpellier, France.
Olivia VilleronceCentre National de la Recherche Scientifique, UMR5203, Institut de Génomique Fonctionnelle, Montpellier, France.
Luke ZappiaDepartment of Pathology, University of Melbourne, Parkville, Victoria, Australia.
Ebba Louise LagerqvistCentre National de la Recherche Scientifique, UMR5203, Institut de Génomique Fonctionnelle, Montpellier, France.
Sebastian LunkeDepartment of Pathology, University of Melbourne, Parkville, Victoria, Australia.
Emmanuelle Charafe-JauffretCentre de Recherche en Cancérologie de Marseille, U1068 Inserm, Marseille, France.
Kym PhamDepartment of Pathology, University of Melbourne, Parkville, Victoria, Australia.
Christina MolckDepartment of Pathology, University of Melbourne, Parkville, Victoria, Australia.
Nathalie RollandService d'anatomopathologie, CHU Carémeau, Nîmes, France.
Jean François BourgauxService d'Hépato-Gastroentérologie, CHU Carémeau, Nîmes, France.
Michel PrudhommeService de Chirurgie Digestive, CHU Carémeau, Nîmes, France.
Claire PhilippeService de Chirurgie Digestive, CHU Carémeau, Nîmes, France.
Sophie BravoLaboratoire de Biochimie, CHU Carémeau, Nîmes, France.
Jean Christophe BoyerLaboratoire de Biochimie, CHU Carémeau, Nîmes, France.
Lucile Canterel-ThouennonPlateforme MPCC-SIRIC Montpellier Cancer, IRCM, Montpellier, France.
Graham Roy TaylorDepartment of Pathology, University of Melbourne, Parkville, Victoria, Australia.
Arthur HsuDepartment of Pathology, University of Melbourne, Parkville, Victoria, Australia.
Jean Marc PascussiCentre National de la Recherche Scientifique, UMR5203, Institut de Génomique Fonctionnelle, Montpellier, France.
Frédéric HollandeCentre National de la Recherche Scientifique, UMR5203, Institut de Génomique Fonctionnelle, Montpellier, France.
Julie PannequinCentre National de la Recherche Scientifique, UMR5203, Institut de Génomique Fonctionnelle, Montpellier, France.
University of Melbourne · AUCentre Hospitalier Universitaire de Nîmes · FRUniversité de Montpellier · FRCentre National pour la Recherche Scientifique et Technique (CNRST) · MACentre de Recherche en Cancérologie de Marseille · FRDigestive Care (United States) · USInserm · FRInstitut de Génomique Fonctionnelle · FRInstitut de Recherche en Cancérologie de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAlthough counting of circulating tumour cells (CTC) has attracted a broad interest as potential markers of tumour progression and treatment response, the lack of functional characterisation of these cells had become a bottleneck in taking these observations to the clinic. Our objective was to culture these cells in order to understand them and exploit their therapeutic potential to the full.

designHere, hypothesising that some CTC potentially have cancer stem cell (CSC) phenotype, we generated several CTC lines from the blood of patients with advanced metastatic colorectal cancer (CRC) based on their self-renewal abilities. Multiple standard tests were then employed to characterise these cells.

resultsOur CTC lines self-renew, express CSC markers and have multilineage differentiation ability, both

conclusionsTaken together, our results directly demonstrate the existence of patient-derived colorectal CTCs that bear all the functional attributes of CSCs. The CTC culture model described here is simple and takes <1 month from blood collection to drug testing, therefore, routine clinical application could facilitate access to personalised medicine. CLINICAL

trial registrationClinicalTrial.gov NCT01577511.

Indexed as

Aldehyde DehydrogenaseAldehyde Dehydrogenase 1 FamilyAnimalsAntineoplastic AgentsCell DifferentiationCell Self RenewalColorectal NeoplasmsDipeptidyl Peptidase 4Drug Resistance, NeoplasmHumansHyaluronan ReceptorsInactivation, MetabolicLiver NeoplasmsMiceNeoplasm TransplantationNeoplastic Cells, CirculatingAldehyde DehydrogenaseAldehyde Dehydrogenase 1 FamilyALDH1A1 protein, humanAntineoplastic AgentsCD44v6 antigenDipeptidyl Peptidase 4Hyaluronan ReceptorsRetinal DehydrogenaseRNA, NeoplasmCOLORECTAL CANCERDRUG TOXICITYLIVER METASTASES

Identifiers

PMID27456153
PMCPMC5595103
OpenAlexW2491418081

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.