Evidence map›Paper›PMID 22451267›Full record

ArticleMolecular medicine (Cambridge, Mass.)2012

Inhibition of α-SMA by the ectodomain of FGFR2c attenuates lung fibrosis.

Wang Ju, Yu Zhihong, Zhou Zhiyou, Huang Qin, Wang Dingding, Sun Li, Zhu Baowei, Wei Xing, He Ying, Hong An

Open access · goldAbstract read
In one paragraph

Article in Molecular medicine (Cambridge, Mass.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

23 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. The Inhibitory Effects of Naringin in a Rat Model of Postoperative Intraperitoneal Adhesion Formation.Evidence-based complementary and alternative medicine : eCAM · 2022
    Article
  5. Review
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  7. Cooperative signaling between integrins and growth factor receptors in fibrosis.Journal of molecular medicine (Berlin, Germany) · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. The effect of human amniotic epithelial cells on urethral stricture fibroblasts.Journal of clinical and translational research · 2019
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Thymic Stromal Lymphopoietin Promotes Fibrosis and Activates Mitogen-Activated Protein Kinases in MRC-5 Cells.Medical science monitor : international medical journal of experimental and clinical research · 2016
    Article
  18. Article
  19. Attenuating endogenous Fgfr2b ligands during bleomycin-induced lung fibrosis does not compromise murine lung repair.American journal of physiology. Lung cellular and molecular physiology · 2015
    Article
  20. Review
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 at 2 institutions in 1 country.

Wang JuGuangdong Provincial Key Laboratory of Bioengineering Medicine (National Engineering Research Centre of Genetic Medicine), Guangzhou, Guangdong China. wang_ju1688@yahoo.cn
Yu Zhihong
Zhou Zhiyou
Huang Qin
Wang Dingding
Sun Li
Zhu Baowei
Wei Xing
He Ying
Hong An
Key Laboratory of Guangdong Province · CNGuangdong Pharmaceutical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The soluble ectodomain of fibroblast growth factor receptor-IIIc (sFGFR2c) is able to bind to fibroblast growth factor (FGF) ligands and block the activation of the FGF-signaling pathway. In this study, sFGFR2c inhibited lung fibrosis dramatically in vitro and in vivo. The upregulation of α-smooth muscle actin (α-SMA) in fibroblasts by transforming growth factor-β1 (TGF-β1) is an important step in the process of lung fibrosis, in which FGF-2, released by TGF-β1, is involved. sFGFR2c inhibited α-SMA induction by TGF-β1 via both the extracellular signal-regulated kinase 1/2 (ERK1/2) and Smad3 pathways in primary mouse lung fibroblasts and the proliferation of mouse lung fibroblasts. In a mouse model of bleomycin (BLM)-induced lung fibrosis, mice were treated with sFGFR2c from d 3 or d 10 to 31 after BLM administration. Then we used hematoxylin and eosin staining, Masson staining and immunohistochemical staining to evaluate the inhibitory effects of sFGFR2c on lung fibrosis. The treatment with sFGFR2c resulted in significant attenuation of the lung fibrosis score and collagen deposition. The expression levels of α-SMA, p-FGFRs, p-ERK1/2 and p-Smad3 in the lungs of sFGFR2c-treated mice were markedly lower. sFGFR2c may have potential for the treatment of lung fibrosis as an FGF-2 antagonist.

Indexed as

ActinsAnimalsBleomycinCell ProliferationCells, CulturedDisease Models, AnimalEnzyme ActivationFibroblast Growth Factor 2FibroblastsGene Expression RegulationHumansMaleMAP Kinase Signaling SystemMiceMice, Inbred C57BLPneumoniaActinsalpha-smooth muscle actin, mouseBleomycinFibroblast Growth Factor 2Protein IsoformsReceptor, Fibroblast Growth Factor, Type 2Smad ProteinsTransforming Growth Factor beta1

Identifiers

PMID22451267
PMCPMC3459475
OpenAlexW1870635976

What OpenQuestion holds

Textmetadata
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.