Evidence map›Paper›PMID 32793478›Full record

ReviewFrontiers in oncology2020

Intrinsic and Extrinsic Modulators of the Epithelial to Mesenchymal Transition: Driving the Fate of Tumor Microenvironment.

Edoardo D'Angelo, Rafael Soares Lindoso, Francesca Sensi, Salvatore Pucciarelli, Benedetta Bussolati, Marco Agostini, Federica Collino

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  5. Optogenetic control of YAP can enhance the rate of wound healing.Cellular & molecular biology letters · 2023
    Article
  6. International journal of molecular sciences · 2023
    Article
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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

7 authors at 5 institutions in 3 countries.

Edoardo D'AngeloFirst Surgical Clinic, Department of Surgery, Oncology and Gastroenterology, University of Padova, Padua, Italy.
Rafael Soares LindosoInstitute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Francesca SensiInstitute of Pediatric Research, Fondazione Citta della Speranza, Padua, Italy.
Salvatore PucciarelliFirst Surgical Clinic, Department of Surgery, Oncology and Gastroenterology, University of Padova, Padua, Italy.
Benedetta BussolatiDepartment of Medical Sciences, Molecular Biotechnology Center, University of Torino, Turin, Italy.
Marco AgostiniFirst Surgical Clinic, Department of Surgery, Oncology and Gastroenterology, University of Padova, Padua, Italy.
Federica CollinoInstitute of Biophysics Carlos Chagas Filho, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
University of Padua · ITCa' Foscari University of Venice · ITConsorzio per la Ricerca Sanitaria · ITFundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro · BRUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The epithelial to mesenchymal transition (EMT) is an evolutionarily conserved process. In cancer, EMT can activate biochemical changes in tumor cells that enable the destruction of the cellular polarity, leading to the acquisition of invasive capabilities. EMT regulation can be triggered by intrinsic and extrinsic signaling, allowing the tumor to adapt to the microenvironment demand in the different stages of tumor progression. In concomitance, tumor cells undergoing EMT actively interact with the surrounding tumor microenvironment (TME) constituted by cell components and extracellular matrix as well as cell secretome elements. As a result, the TME is in turn modulated by the EMT process toward an aggressive behavior. The current review presents the intrinsic and extrinsic modulators of EMT and their relationship with the TME, focusing on the non-cell-derived components, such as secreted metabolites, extracellular matrix, as well as extracellular vesicles. Moreover, we explore how these modulators can be suitable targets for anticancer therapy and personalized medicine.

Indexed as

epithelial to mesenchymal transitionextracellular matrixextracellular vesiclespersonalized medicinetumor microenvironment

Identifiers

PMID32793478
PMCPMC7393251
OpenAlexW3044042323

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.