Evidence map›Paper›PMID 41743400›Full record

ArticleTargets (Basel)2025

Pathology and Therapeutic Significance of Fibroblast Growth Factors.

Oshadi Edirisinghe, Gaëtane Ternier, Thallapuranam Krishnaswamy Suresh Kumar

Abstract read
In one paragraph

Article in Targets (Basel), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Decoding the Function ofAnimals : an open access journal from MDPI · 2025
    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

3 authors.

Oshadi EdirisingheCell and Molecular Biology Program, University of Arkansas, Fayetteville, AR 72701, USA.
Gaëtane TernierDepartment of Chemistry and Biochemistry, University of Arkansas, Fayetteville, AR 72701, USA.
Thallapuranam Krishnaswamy Suresh KumarCell and Molecular Biology Program, University of Arkansas, Fayetteville, AR 72701, USA.

Funding

Unraveling Gene-Environment Interactions Shaping Metabolism: A Multi-Omics Analysis in DrosophilaP20GM139768 · NIGMS · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI Joanna Fiddler · 2021 to 2026
$17.0M
Hyperstable FGF1-FGF2 based therapeutic formulation for wound careR15GM154267 · NIGMS · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI THALLAPURANAM, SURESH KUMAR KRISHNASWAMY · 2024 to 2024
$435k
NIGMS NIH HHS P20 GM139768NIGMS NIH HHS R15 GM154267
6 · The paper itself

Abstract

The fibroblast growth factor (FGF) family includes 22 proteins in humans. Based on their mode of action, there are three families of FGFs: paracrine FGFs (FGF 1-10, 16, 17, 18, 20, and 22), intracrine FGFs (FGF 11-14), and endocrine FGFs (FGF 19, 21, and 23). FGF signaling plays critical roles in embryonic development, tissue repair, regeneration, angiogenesis, and metabolic regulation. They exert their cellular functions by binding, dimerization, and activation of transmembrane FGF receptors (FGFRs). Aberrant FGF signaling is associated with various human diseases. Thus, understanding the unique properties of FGF signaling will help to explore new therapeutic interventions against FGF-mediated pathological conditions. This review will discuss the differential expression and regulation of each FGF under normal human physiological and pathological conditions. Moreover, we will outline current therapeutics and treatment strategies that have been developed against FGF-related pathology.

Indexed as

FGFFGFRFGF signalingfibroblast growth factor receptorsfibroblast growth factors

Identifiers

PMID41743400
PMCPMC12931840

What OpenQuestion holds

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LicenceCC BY
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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.