Evidence map›Paper›PMID 30443492›Full record

ArticleFrontiers in oncology2018

Long Pentraxin 3-Mediated Fibroblast Growth Factor Trapping Impairs Fibrosarcoma Growth.

Priscila Fabiana Rodrigues, Sara Matarazzo, Federica Maccarinelli, Eleonora Foglio, Arianna Giacomini, João Paulo Silva Nunes, Marco Presta, Adriana Abalen Martins Dias, Roberto Ronca

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Role of long pentraxin PTX3 in cancer.Clinical and experimental medicine · 2023
    Review
  3. Article
  4. Review
  5. Insights into the Relationship between Pentraxin-3 and Cancer.International journal of molecular sciences · 2022
    Review
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  7. Article
  8. Article
  9. Review
  10. 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

9 authors at 2 institutions in 2 countries.

Priscila Fabiana RodriguesLaboratory of Inflammation and Cancer, Department of General Biology - ICB, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Sara MatarazzoDepartment of Molecular and Translational Medicine, School of Medicine, University of Brescia, Brescia, Italy.
Federica MaccarinelliDepartment of Molecular and Translational Medicine, School of Medicine, University of Brescia, Brescia, Italy.
Eleonora FoglioDepartment of Molecular and Translational Medicine, School of Medicine, University of Brescia, Brescia, Italy.
Arianna GiacominiDepartment of Molecular and Translational Medicine, School of Medicine, University of Brescia, Brescia, Italy.
João Paulo Silva NunesLaboratory of Inflammation and Cancer, Department of General Biology - ICB, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Marco PrestaDepartment of Molecular and Translational Medicine, School of Medicine, University of Brescia, Brescia, Italy.
Adriana Abalen Martins DiasLaboratory of Inflammation and Cancer, Department of General Biology - ICB, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Roberto RoncaDepartment of Molecular and Translational Medicine, School of Medicine, University of Brescia, Brescia, Italy.
University of Brescia · ITUniversidade Federal de Minas Gerais · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibrosarcomas are soft tissue mesenchymal tumors originating from transformed fibroblasts. Fibroblast growth factor-2 (FGF2) and its tyrosine-kinase receptors (FGFRs) play pivotal roles in fibrosarcoma onset and progression, FGF2 being actively produced by fibroblasts in all stages along their malignant transformation to the fibrosarcoma stage. The soluble pattern recognition receptor long pentraxin-3 (PTX3) is an extrinsic oncosuppressor whose expression is reduced in different tumor types, including soft tissue sarcomas, via hypermethylation of its gene promoter. PTX3 interacts with FGF2 and other FGF family members, thus acting as a multi-FGF antagonist able to inhibit FGF-dependent neovascularization and tumor growth. Here, PTX3 overexpression significantly reduced the proliferative and tumorigenic potential of fibrosarcoma cells

Indexed as

FGFFGFRFGF-trapfibrosarcomalong pentraxin-3

Identifiers

PMID30443492
PMCPMC6221954
OpenAlexW2899209527

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.