Evidence map›Paper›PMID 26332583›Full record

ArticlePloS one2015

Altered FGF Signaling Pathways Impair Cell Proliferation and Elevation of Palate Shelves.

Weijie Wu, Shuping Gu, Cheng Sun, Wei He, Xiaohua Xie, Xihai Li, Wenduo Ye, Chunlin Qin, Yiping Chen, Jing Xiao and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Frontiers in cell and developmental biology · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Frontiers in cell and developmental biology · 2021
    Article
  9. Frontiers in physiology · 2021
    Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Frontiers in physiology · 2017
    Article
  16. Article
  17. Article
  18. 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

11 authors at 4 institutions in 2 countries.

Weijie WuDepartment of Stomatology, Shanghai Zhongshan Hospital, Shanghai, China; Department of Cell & Molecular Biology, Sciences and Engineering School, Tulane University, New Orleans, Louisiana, United States of America.
Shuping GuDepartment of Cell & Molecular Biology, Sciences and Engineering School, Tulane University, New Orleans, Louisiana, United States of America.
Cheng SunDepartment of Cell & Molecular Biology, Sciences and Engineering School, Tulane University, New Orleans, Louisiana, United States of America.
Wei HeDepartment of Cell & Molecular Biology, Sciences and Engineering School, Tulane University, New Orleans, Louisiana, United States of America; Department of Oral and Maxillofacial Surgery, Affiliated Stomatological Hospital, Zunyi Medical University, Zunyi, China.
Xiaohua XieDepartment of Biomedical Sciences, Baylor College of Dentistry, Texas A&M Health Sciences Center, Dallas, Texas, United States of America; Department of Endodontics, Institute of Hard Tissue Development and Regeneration, the 2nd Affiliated Hospital of Harbin Medical University, Harbin, China.
Xihai LiDepartment of Cell & Molecular Biology, Sciences and Engineering School, Tulane University, New Orleans, Louisiana, United States of America; Academy of Integrative Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou, China.
Wenduo YeDepartment of Cell & Molecular Biology, Sciences and Engineering School, Tulane University, New Orleans, Louisiana, United States of America.
Chunlin QinDepartment of Biomedical Sciences, Baylor College of Dentistry, Texas A&M Health Sciences Center, Dallas, Texas, United States of America.
Yiping ChenDepartment of Cell & Molecular Biology, Sciences and Engineering School, Tulane University, New Orleans, Louisiana, United States of America.
Jing XiaoDepartment of Oral Biology, College of Stomatology, Dalian Medical University, Dalian, China.
Chao LiuDepartment of Cell & Molecular Biology, Sciences and Engineering School, Tulane University, New Orleans, Louisiana, United States of America; Department of Biomedical Sciences, Baylor College of Dentistry, Texas A&M Health Sciences Center, Dallas, Texas, United States of America; Department of Oral Biology, College of Stomatology, Dalian Medical University, Dalian, China.
Tulane University · USDalian Medical University · CNHarbin Medical University · CNZunyi Medical University · CN

Funding

Growth Factor Signaling in Mouse PalatogensisR01DE014044 · NIDCR · TULANE UNIVERSITY OF LOUISIANA · PI CHEN, YIPING · 2002 to 2013
$3.4M
The Roles of FAM20C (DMP4) in Odontogenesis and OsteogenesisR01DE022549 · NIDCR · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI QIN, CHUNLIN · 2013 to 2017
$1.8M
NIDCR NIH HHS R01 DE014044NIDCR NIH HHS R01 DE022549NIDCR NIH HHS R01 DE14044
6 · The paper itself

Abstract

In palatogenesis, palatal shelves are patterned along the mediolateral axis as well as the anteroposterior axis before the onset of palatal fusion. Fgf10 specifically expressed in lateral mesenchyme of palate maintains Shh transcription in lateral epithelium, while Fgf7 activated in medial mesenchyme by Dlx5, suppressed the expansion of Shh expression to medial epithelium. How FGF signaling pathways regulate the cell behaviors of developing palate remains elusive. In our study, we found that when Fgf8 is ectopically expressed in the embryonic palatal mesenchyme, the elevation of palatal shelves is impaired and the posterior palatal shelves are enlarged, especially in the medial side. The palatal deformity results from the drastic increase of cell proliferation in posterior mesenchyme and decrease of cell proliferation in epithelium. The expression of mesenchymal Fgf10 and epithelial Shh in the lateral palate, as well as the Dlx5 and Fgf7 transcription in the medial mesenchyme are all interrupted, indicating that the epithelial-mesenchymal interactions during palatogenesis are disrupted by the ectopic activation of mesenchymal Fgf8. Besides the altered Fgf7, Fgf10, Dlx5 and Shh expression pattern, the reduced Osr2 expression domain in the lateral mesenchyme also suggests an impaired mediolateral patterning of posterior palate. Moreover, the ectopic Fgf8 expression up-regulates pJak1 throughout the palatal mesenchyme and pErk in the medial mesenchyme, but down-regulates pJak2 in the epithelium, suggesting that during normal palatogenesis, the medial mesenchymal cell proliferation is stimulated by FGF/Erk pathway, while the epithelial cell proliferation is maintained through FGF/Jak2 pathway.

Indexed as

Cell ProliferationGene Expression Regulation, DevelopmentalAnimalsCleft PalateFibroblast Growth Factor 8Hedgehog ProteinsMicePalateRNA, UntranslatedSignal TransductionTranscription FactorsUp-RegulationFgf8 protein, mouseFibroblast Growth Factor 8Gt(ROSA)26Sor non-coding RNA, mouseHedgehog ProteinsOsr2 protein, mouseRNA, UntranslatedShh protein, mouseTranscription Factors

Identifiers

PMID26332583
PMCPMC4558018
OpenAlexW1851483244

What OpenQuestion holds

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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.