Evidence map›Paper›PMID 40332096›Full record

ArticleInternational journal of molecular sciences2025

The Clinical Relevance of Epithelial-to-Mesenchymal Transition Hallmarks: A Cut-Off-Based Approach in Healthy and Cancerous Cell Lines.

Maria Cristina Rapanotti, Elisa Cugini, Maria Giovanna Scioli, Tonia Cenci, Silvia Anzillotti, Martina Puzzuoli, Alessandro Terrinoni, Amedeo Ferlosio, Anastasia De Luca, Augusto Orlandi

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
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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.

Maria Cristina RapanottiAnatomic Pathology, Department of Integrated Care Processes, University of Rome Tor Vergata, Viale Oxford 81, 00133 Rome, Italy.
Elisa CuginiAnatomic Pathology, Department of Integrated Care Processes, University of Rome Tor Vergata, Viale Oxford 81, 00133 Rome, Italy.
Maria Giovanna ScioliAnatomic Pathology, Department of Integrated Care Processes, University of Rome Tor Vergata, Viale Oxford 81, 00133 Rome, Italy.ORCID 0000-0002-8458-4108
Tonia CenciAnatomic Pathology, Department of Integrated Care Processes, University of Rome Tor Vergata, Viale Oxford 81, 00133 Rome, Italy.ORCID 0000-0002-6272-4587
Silvia AnzillottiAnatomic Pathology, Department of Integrated Care Processes, University of Rome Tor Vergata, Viale Oxford 81, 00133 Rome, Italy.ORCID 0009-0001-0764-0495
Martina PuzzuoliAnatomic Pathology, Department of Integrated Care Processes, University of Rome Tor Vergata, Viale Oxford 81, 00133 Rome, Italy.
Alessandro TerrinoniDepartment of Laboratory Medicine, Tor Vergata University Hospital, 00133 Rome, Italy.ORCID 0000-0002-7442-2252
Amedeo FerlosioAnatomic Pathology, Department of Integrated Care Processes, University of Rome Tor Vergata, Viale Oxford 81, 00133 Rome, Italy.
Anastasia De LucaDepartment of Biology, University of Rome Tor Vergata, Via della Ricerca Scientifica 1, 00133 Rome, Italy.ORCID 0000-0002-6532-989X
Augusto OrlandiAnatomic Pathology, Department of Integrated Care Processes, University of Rome Tor Vergata, Viale Oxford 81, 00133 Rome, Italy.ORCID 0000-0001-7202-5854

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The atypical activation of the epithelial-to-mesenchymal transition represents one of the main mechanisms driving cancer cell dissemination. It enables epithelial cancer cells to detach from the primary tumor mass and gain survival advantages in the bloodstream, significantly contributing to the spread of circulating tumor cells. Notably, epithelial-to-mesenchymal transition is not a binary process but rather leads to the formation of a wide range of cell subpopulations characterized by the simultaneous expression of both epithelial and mesenchymal markers. Therefore, analyzing the modulation of EMT hallmarks during the conversion from healthy cells to metastatic cancer cells, which acquire stem mesenchymal characteristics, is of particular interest. This study investigates the expression of a panel of epithelial-to-mesenchymal transition-related genes in healthy cells, primary and metastatic cancer cells, and in mesenchymal cell lines, derived from various tissues, including the lung, colon, pancreas, skin, and neuro-ectoderm, with the aim of identifying potential cut-off values for assessing cancer aggressiveness. Interestingly, we found that the expression levels of

Indexed as

Epithelial-Mesenchymal TransitionNeoplasmsAntigens, CDBiomarkers, TumorCadherinsCell Line, TumorClinical RelevanceGene Expression Regulation, NeoplasticHumansZinc Finger E-box-Binding Homeobox 1Antigens, CDBiomarkers, TumorCadherinsCDH1 protein, humanZEB1 protein, humanZinc Finger E-box-Binding Homeobox 1cancerous cellsepithelial-to-mesenchymal transitionhealthy cellsmesenchymal cells

Identifiers

PMID40332096
PMCPMC12026647

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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.