Evidence map›Paper›PMID 30959764›Full record

ReviewCancers2019

Heterogeneity in Circulating Tumor Cells: The Relevance of the Stem-Cell Subset.

Chiara Agnoletto, Fabio Corrà, Linda Minotti, Federica Baldassari, Francesca Crudele, William Joseph James Cook, Gianpiero Di Leva, Adamo Pio d'Adamo, Paolo Gasparini, Stefano Volinia

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
10.2field-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.

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

92 citing papers in PubMed, 142 citations in OpenAlex.

  1. Trial
  2. Review
  3. Circulating Tumor Cells: Emerging Frontiers in Cancer Technology.Expert reviews in molecular medicine · 2026
    Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
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  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
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  19. Article
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32 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

10 authors at 3 institutions in 2 countries.

Chiara AgnolettoDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, 44121 Ferrara, Italy. gnlchr@unife.it.ORCID 0000-0002-1363-5852
Fabio CorràDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, 44121 Ferrara, Italy. crrfba@unife.it.
Linda MinottiDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, 44121 Ferrara, Italy. mntlnd@unife.it.ORCID 0000-0003-2116-8411
Federica BaldassariDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, 44121 Ferrara, Italy. bldfrc1@unife.it.
Francesca CrudeleDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, 44121 Ferrara, Italy. crdfnc@unife.it.ORCID 0000-0003-4638-9122
William Joseph James CookSchool of Environment and Life Sciences, University of Salford, Salford M5 4WT, UK. w.j.j.cook@edu.salford.ac.uk.ORCID 0000-0003-3735-6134
Gianpiero Di LevaSchool of Environment and Life Sciences, University of Salford, Salford M5 4WT, UK. G.DiLeva@salford.ac.uk.
Adamo Pio d'AdamoDepartment of Medicine, Surgery and Health Sciences, University of Trieste, 34127 Trieste, Italy. adamopio.dadamo@burlo.trieste.it.ORCID 0000-0001-9367-4909
Paolo GaspariniDepartment of Medicine, Surgery and Health Sciences, University of Trieste, 34127 Trieste, Italy. paolo.gasparini@burlo.trieste.it.
Stefano VoliniaDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, 44121 Ferrara, Italy. s.volinia@unife.it.
University of Ferrara · ITUniversity of Salford · GBUniversity of Trieste · IT

Funding

Associazione Italiana Ricerca sul Cancro AIRC IG 17063Italian PRIN MIUR 2010 2010W4J4RM
6 · The paper itself

Abstract

The release of circulating tumor cells (CTCs) into vasculature is an early event in the metastatic process. The analysis of CTCs in patients has recently received widespread attention because of its clinical implications, particularly for precision medicine. Accumulated evidence documents a large heterogeneity in CTCs across patients. Currently, the most accepted view is that tumor cells with an intermediate phenotype between epithelial and mesenchymal have the highest plasticity. Indeed, the existence of a meta-stable or partial epithelial⁻mesenchymal transition (EMT) cell state, with both epithelial and mesenchymal features, can be easily reconciled with the concept of a highly plastic stem-like state. A close connection between EMT and cancer stem cells (CSC) traits, with enhanced metastatic competence and drug resistance, has also been described. Accordingly, a subset of CTCs consisting of CSC, present a stemness profile, are able to survive chemotherapy, and generate metastases after xenotransplantation in immunodeficient mice. In the present review, we discuss the current evidence connecting CTCs, EMT, and stemness. An improved understanding of the CTC/EMT/CSC connections may uncover novel therapeutic targets, irrespective of the tumor type, since most cancers seem to harbor a pool of CSCs, and disclose important mechanisms underlying tumorigenicity.

Indexed as

CSCCTCEMTstemness

Identifiers

PMID30959764
PMCPMC6521045
OpenAlexW2926623958

What Socratic 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 Socratic graph.