Evidence map›Paper›PMID 38988879›Full record

ReviewF1000Research2024

Essential growth factor receptors for fibroblast homeostasis and activation: Fibroblast Growth Factor Receptor (FGFR), Platelet Derived Growth Factor Receptor (PDGFR), and Transforming Growth Factor β Receptor (TGFβR).

Maye F Cheng, Faizah S Abdullah, Matthew B Buechler

Abstract readReview
In one paragraph

Review in F1000Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. 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.

Maye F Cheng *Immunology, University of Toronto, Toronto, ON, M5S 1A8, Canada.ORCID https://orcid.org/0000-0003-1902-622X
Faizah S Abdullah *Immunology, University of Toronto, Toronto, ON, M5S 1A8, Canada.ORCID https://orcid.org/0009-0008-9775-4015
Matthew B BuechlerImmunology, University of Toronto, Toronto, ON, M5S 1A8, Canada.ORCID https://orcid.org/0000-0003-1902-622X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibroblasts are cells of mesenchymal origin that are found throughout the body. While these cells have several functions, their integral roles include maintaining tissue architecture through the production of key extracellular matrix components, and participation in wound healing after injury. Fibroblasts are also key mediators in disease progression during fibrosis, cancer, and other inflammatory diseases. Under these perturbed states, fibroblasts can activate into inflammatory fibroblasts or contractile myofibroblasts. Fibroblasts require various growth factors and mitogenic molecules for survival, proliferation, and differentiation. While the activity of mitogenic growth factors on fibroblasts

Indexed as

FibroblastsHomeostasisReceptors, Fibroblast Growth FactorReceptors, Platelet-Derived Growth FactorAnimalsHumansReceptors, Transforming Growth Factor betaReceptors, Fibroblast Growth FactorReceptors, Platelet-Derived Growth FactorReceptors, Transforming Growth Factor betaFGFRFibroblastsgrowth factor receptorsgrowth factorsPDGFRTGF-b

Identifiers

PMID38988879
PMCPMC11234085

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.