Evidence map›Paper›PMID 31056474›Full record

ArticleEBioMedicine2019

Stemness underpinning all steps of human colorectal cancer defines the core of effective therapeutic strategies.

Alberto Visioli, Fabrizio Giani, Nadia Trivieri, Riccardo Pracella, Elide Miccinilli, Maria Grazia Cariglia, Orazio Palumbo, Andrea Arleo, Fabio Dezi, Massimiliano Copetti and 13 more

Abstract read
In one paragraph

Article in EBioMedicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–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

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Circulating Tumor Cells: Emerging Frontiers in Cancer Technology.Expert reviews in molecular medicine · 2026
    Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Growth factor independence underpins a paroxysmal, aggressive Wnt5aJournal of experimental & clinical cancer research : CR · 2022
    Article
  11. Article
  12. Review
  13. BRAFJournal of experimental & clinical cancer research : CR · 2020
    Article
  14. Article
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

23 authors.

Alberto VisioliStemGen SpA, Milan, Italy.
Fabrizio GianiStemGen SpA, Milan, Italy.
Nadia TrivieriFondazione IRCCS Casa Sollievo della Sofferenza, Cancer Stem Cells Unit, ISBReMIT, Foggia, Italy.
Riccardo PracellaFondazione IRCCS Casa Sollievo della Sofferenza, Cancer Stem Cells Unit, ISBReMIT, Foggia, Italy.
Elide MiccinilliFondazione IRCCS Casa Sollievo della Sofferenza, Cancer Stem Cells Unit, ISBReMIT, Foggia, Italy.
Maria Grazia CarigliaFondazione IRCCS Casa Sollievo della Sofferenza, Cancer Stem Cells Unit, ISBReMIT, Foggia, Italy.
Orazio PalumboFondazione IRCCS Casa Sollievo della Sofferenza, Medical Genetics Unit, Foggia, Italy.
Andrea ArleoFondazione IRCCS Casa Sollievo della Sofferenza, Cancer Stem Cells Unit, ISBReMIT, Foggia, Italy.
Fabio DeziFondazione IRCCS Casa Sollievo della Sofferenza, Cancer Stem Cells Unit, ISBReMIT, Foggia, Italy.
Massimiliano CopettiFondazione IRCCS Casa Sollievo della Sofferenza, Biostatistic Unit, Foggia, Italy.
Laura CajolaStemGen SpA, Milan, Italy.
Silvia RestelliStemGen SpA, Milan, Italy.
Valerio PapaDigestive Surgery Unit, IRCCS "A. Gemelli", Catholic University of the Sacred Heart, Rome, Italy.
Antonio SciutoIRCCS Casa Sollievo della Sofferenza, Abdominal Surgery Unit, Foggia, Italy.
Tiziana Pia LatianoIRCCS Casa Sollievo della Sofferenza, Unit of Oncology, Fogga, Italy.
Massimo CarellaFondazione IRCCS Casa Sollievo della Sofferenza, Medical Genetics Unit, Foggia, Italy.
Dino AmadoriIstituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS Meldola, Italy.
Giulia GalleraniIstituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST) IRCCS Meldola, Biosciences Laboratory, Italy.
Riccardo RicciDepartment of Pathology, IRCCS "A. Gemelli", Catholic University of the Sacred Heart, Rome, Italy.
Sergio AlfieriDepartment of Pathology, IRCCS "A. Gemelli", Catholic University of the Sacred Heart, Rome, Italy.
Graziano PesoleIstituto di Biomembrane, Bioenergetica e Biotecnologie Molecolari del Consiglio Nazionale delle Ricerche, Bari, Italy; Dipartimento di Bioscienze, Biotecnologie e Biofarmaceutica dell'Università di Bari "A. Moro". Bari, Italy.
Angelo L VescoviFondazione IRCCS Casa Sollievo della Sofferenza, Cancer Stem Cells Unit, ISBReMIT, Foggia, Italy; Hyperstem SA, Lugano, Switzerland. Electronic address: vescovia@gmail.com.
Elena BindaFondazione IRCCS Casa Sollievo della Sofferenza, Cancer Stem Cells Unit, ISBReMIT, Foggia, Italy. Electronic address: e.binda@css-mendel.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite their lethality and ensuing clinical and therapeutic relevance, circulating tumor cells (CTCs) from colorectal carcinoma (CRC) remain elusive, poorly characterized biological entities. METHODS AND

findingsWe perfected a cell system of stable, primary lines from human CRC showing that they possess the full complement of ex- and in-vivo, in xenogeneic models, characteristics of CRC stem cells (CCSCs). Here we show how tumor-initiating, CCSCs cells can establish faithful orthotopic phenocopies of the original disease, which contain cells that spread into the circulatory system. While in the vascular bed, these cells retain stemness, thus qualifying as circulating CCSCs (cCCSCs). This is followed by the establishment of lesions in distant organs, which also contain resident metastatic CCSCs (mCCSCs).

interpretationOur results support the concept that throughout all the stages of CRC, stemness is retained as a continuous property by some of their tumor cells. Importantly, we describe a useful standardized model that can enable isolation and stable perpetuation of human CRC's CCSCs, cCCSCs and mCCSCs, providing a useful platform for studies of CRC initiation and progression that is suitable for the discovery of reliable stage-specific biomarkers and the refinement of new patient-tailored therapies. FUND: This work was financially supported by grants from "Ministero della Salute Italiano"(GR-2011-02351534, RC1703IC36 and RC1803IC35) to Elena Binda and from "Associazione Italiana Cancro" (IG-14368) Angelo L. Vescovi. None of the above funders have any role in study design, data collection, data analysis, interpretation, writing the project.

Indexed as

Cell Self RenewalAnimalsBiomarkersCell Transformation, NeoplasticColorectal NeoplasmsDisease Models, AnimalDNA Copy Number VariationsEpithelial-Mesenchymal TransitionFluorescent Antibody TechniqueHeterograftsHumansImmunohistochemistryLoss of HeterozygosityMiceNeoplasm GradingNeoplasm StagingBiomarkersAnti-CRC SCs strategiesCRC biology and biomarkersCRC circulating stem cellsCRC metastatic stem cellsCRC stem cellsHuman colorectal carcinoma (CRC)Stemness

Identifiers

PMID31056474
PMCPMC6603803

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LicenceCC BY-NC-ND
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Registered trials

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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.