Evidence map›Paper›PMID 31557946›Full record

ReviewCells2019

CTC-Derived Models: A Window into the Seeding Capacity of Circulating Tumor Cells (CTCs).

Tala Tayoun, Vincent Faugeroux, Marianne Oulhen, Agathe Aberlenc, Patrycja Pawlikowska, Françoise Farace

Abstract readReview
In one paragraph

Review in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
–field-weighted citation impact
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

83 citing papers in PubMed.

  1. Trial
  2. Article
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  4. Review
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  7. Circulating Tumor Cells: Emerging Frontiers in Cancer Technology.Expert reviews in molecular medicine · 2026
    Review
  8. Article
  9. Article
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  11. Review
  12. Review
  13. Article
  14. Minimal Residual Disease in Metastatic Soft Tissue Sarcoma.Current treatment options in oncology · 2025
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review

23 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

6 authors.

Tala Tayoun"Circulating Tumor Cells" Translational Platform, CNRS UMS3655 - INSERM US23AMMICA, Gustave Roussy, Université Paris-Saclay, F-94805 Villejuif, France. tala.tayoun@gustaveroussy.fr.
Vincent Faugeroux"Circulating Tumor Cells" Translational Platform, CNRS UMS3655 - INSERM US23AMMICA, Gustave Roussy, Université Paris-Saclay, F-94805 Villejuif, France. vincent.faugeroux@laposte.net.
Marianne Oulhen"Circulating Tumor Cells" Translational Platform, CNRS UMS3655 - INSERM US23AMMICA, Gustave Roussy, Université Paris-Saclay, F-94805 Villejuif, France. marianne.oulhen@gustaveroussy.fr.
Agathe Aberlenc"Circulating Tumor Cells" Translational Platform, CNRS UMS3655 - INSERM US23AMMICA, Gustave Roussy, Université Paris-Saclay, F-94805 Villejuif, France. agathe.aberlenc@gustaveroussy.fr.
Patrycja PawlikowskaINSERM, U981 "Identification of Molecular Predictors and new Targets for Cancer Treatment", F-94805 Villejuif, France. patrycjamarta.pawlikowska@gustaveroussy.fr.
Françoise Farace"Circulating Tumor Cells" Translational Platform, CNRS UMS3655 - INSERM US23AMMICA, Gustave Roussy, Université Paris-Saclay, F-94805 Villejuif, France. francoise.farace@gustaveroussy.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastasis is the main cause of cancer-related death owing to the blood-borne dissemination of circulating tumor cells (CTCs) early in the process. A rare fraction of CTCs harboring a stem cell profile and tumor initiation capacities is thought to possess the clonogenic potential to seed new lesions. The highest plasticity has been generally attributed to CTCs with a partial epithelial-to-mesenchymal transition (EMT) phenotype, demonstrating a large heterogeneity among these cells. Therefore, detection and functional characterization of these subclones may offer insight into mechanisms underlying CTC tumorigenicity and inform on the complex biology behind metastatic spread. Although an in-depth mechanistic investigation is limited by the extremely low CTC count in circulation, significant progress has been made over the past few years to establish relevant systems from patient CTCs. CTC-derived xenograft (CDX) models and CTC-derived ex vivo cultures have emerged as tractable systems to explore tumor-initiating cells (TICs) and uncover new therapeutic targets. Here, we introduce basic knowledge of CTC biology, including CTC clusters and evidence for EMT/cancer stem cell (CSC) hybrid phenotypes. We report and evaluate the CTC-derived models generated to date in different types of cancer and shed a light on challenges and key findings associated with these novel assays.

Indexed as

Models, BiologicalAnimalsCarcinogenesisCell Culture TechniquesEpithelial-Mesenchymal TransitionHumansNeoplastic Cells, CirculatingNeoplastic Stem CellsTumor Stem Cell Assaycirculating tumor cells (CTCs)CTC-derived ex vivo modelsCTC-derived xenograftsmetastasistumor-initiating cells (TICs)

Identifiers

PMID31557946
PMCPMC6829286

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.