Evidence map›Paper›PMID 23867472›Full record

ArticleCancer research2013

Rapid induction of lung adenocarcinoma by fibroblast growth factor 9 signaling through FGF receptor 3.

Yongjun Yin, Tomoko Betsuyaku, Joel R Garbow, Jinbai Miao, Ramaswamy Govindan, David M Ornitz

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 56 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Aberrant Expression of FGFRL1 in Esophageal Cancer and Its Regulation by miR-107.Asian Pacific journal of cancer prevention : APJCP · 2023
    Article
  8. Article
  9. Review
  10. Article
  11. FGFR3Cell death & disease · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. FGF receptors control alveolar elastogenesis.Development (Cambridge, England) · 2017
    Article
  18. Article
  19. Article
  20. Drug-sensitive FGFR3 mutations in lung adenocarcinoma.Annals of oncology : official journal of the European Society for Medical Oncology · 2017
    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

6 authors at 2 institutions in 2 countries.

Yongjun YinAuthors' Affiliations: Departments of Developmental Biology, Radiology, and Medicine, Washington University School of Medicine, Saint Louis, Missouri; Division of Pulmonary Medicine, Department of Medicine, Keio University School of Medicine, Tokyo, Japan; and Department of Thoracic Surgery, Beijing Chaoyang Hospital, China Capital Medical University, Beijing, China.
Tomoko Betsuyaku
Joel R Garbow
Jinbai Miao
Ramaswamy Govindan
David M Ornitz
Capital Medical University · CNKeio University · JP

Funding

Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Nicholas O. Davidson · 2000 to 2026
$30.8M
REGULATION OF LUNG DEVELOPMENT BY FGF9 SIGNALING PATHWAYSR01HL111190 · NHLBI · WASHINGTON UNIVERSITY · PI ORNITZ, DAVID M · 2012 to 2020
$3.9M
NHLBI NIH HHS R01 HL111190NIDDK NIH HHS P30 DK052574
6 · The paper itself

Abstract

Fibroblast growth factors (FGF) are expressed in many non-small cell lung carcinoma (NSCLC) primary tumors and derived cell lines, and mutations in FGF receptor 3 (FGFR3) have been identified in human lung adenocarcinoma. FGF9 has been implicated in the pathogenesis of NSCLC by synergizing with EGFR pathways or by providing an escape pathway mediating resistance to EGFR inhibition. To model pathogenic mechanisms mediated by FGF signals, we have established a mouse model in which FGF9 expression can be induced in adult lung epithelium. Here, we show that induced expression of FGF9 in adult lung leads to the rapid proliferation of distal airway epithelial cells that express the stem cell marker, Sca-1, and the proximal and distal epithelial markers, Sftpc and CC10, the rapid formation of Sftpc-positive adenocarcinomas, and eventual metastasis in some mice. Furthermore, we have identified FGFR3 as the obligate receptor mediating the FGF9 oncogenic signal. These results identify an FGF9-FGFR3 signal as a primary oncogenic pathway for lung adenocarcinoma and suggest that this pathway could be exploited for customized therapeutic applications for both primary tumors and those that have acquired resistance to inhibition of other signaling pathways.

Indexed as

Cell ProliferationAdenocarcinomaAnimalsAntigens, LyApoptosisBlotting, WesternCarcinoma, Non-Small-Cell LungDisease Models, AnimalFibroblast Growth Factor 9HumansImmunoenzyme TechniquesIn Situ HybridizationIntercellular Signaling Peptides and ProteinsLung NeoplasmsMagnetic Resonance ImagingMembrane ProteinsAntigens, LyFgf9 protein, mouseFgfr3 protein, mouseFibroblast Growth Factor 9Intercellular Signaling Peptides and ProteinsLy6a protein, mouseMembrane ProteinsPeptidesPulmonary Surfactant-Associated Protein CReceptor, Fibroblast Growth Factor, Type 3RNA, MessengerScgb1a1 protein, mouseSftpc protein, mouseUteroglobin

Identifiers

PMID23867472
PMCPMC3778117
OpenAlexW2155185375

What OpenQuestion holds

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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.