Evidence map›Paper›PMID 23979135›Full record

ArticleThe Journal of biological chemistry2013

Fibroblast growth factor signaling is essential for self-renewal of dental epithelial stem cells.

Julia Yu Fong Chang, Cong Wang, Junchen Liu, Yanqing Huang, Chengliu Jin, Chaofeng Yang, Bo Hai, Fei Liu, Rena N D'Souza, Wallace L McKeehan and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. LGR4 is required for sequential molar development.Biochemistry and biophysics reports · 2016
    Article
  12. Article
  13. 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 2 institutions in 2 countries.

Julia Yu Fong ChangFrom the Center for Cancer and Stem Cell Biology, Institute of Biosciences and Technology, Texas A&M University, Houston, Texas 77030-3303.
Cong Wang
Junchen Liu
Yanqing Huang
Chengliu Jin
Chaofeng Yang
Bo Hai
Fei Liu
Rena N D'Souza
Wallace L McKeehan
Fen Wang
Texas A&M University · USBaylor University · US

Funding

Targeting Tumor Microenvironment-Induced Therapy Resistance in Prostate Cancer Bone MetastasisP50CA140388 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LIN, SUE-HWA · 2009 to 2022
$23.4M
Receptor-specific signaling of FGFR in the prostateR01CA096824 · NCI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI WANG, FEN · 2003 to 2013
$2.5M
Baylor's Scientific Training Program for Dental Academic Researchers: B-STARST32DE018380 · NIDCR · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI SVOBODA, KATHY KAY · 2008 to 2012
$1.7M
Fibroblast Growth Factor signaling in odontogenic epithelial stem/progenitor cellK08DE020883 · NIDCR · UNIVERSITY OF WASHINGTON · PI CHANG, JULIA YU FONG · 2010 to 2014
$417k
FRS2-mediated Signals in Prostatic Tumorigenesis and DevelopmentR56CA096824 · NCI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI WANG, FEN · 2008 to 2008
$302k
Fibroblast Growth Factor Signaling in Odontogenic Epithelial Stem CellsR56DE023106 · NIDCR · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI WANG, FEN · 2013 to 2013
$285k
NCI NIH HHS CA096824NCI NIH HHS CA140388NCI NIH HHS P50 CA140388NCI NIH HHS R01 CA096824NCI NIH HHS R56 CA096824NIDCR NIH HHS K08 DE020883NIDCR NIH HHS K08DE020883NIDCR NIH HHS R56 DE023106NIDCR NIH HHS T32 DE018380NIDCR NIH HHS T32DE018380
6 · The paper itself

Abstract

A constant supply of epithelial cells from dental epithelial stem cell (DESC) niches in the cervical loop (CL) enables mouse incisors to grow continuously throughout life. Elucidation of the cellular and molecular mechanisms underlying this unlimited growth potential is of broad interest for tooth regenerative therapies. Fibroblast growth factor (FGF) signaling is essential for the development of mouse incisors and for maintenance of the CL during prenatal development. However, how FGF signaling in DESCs controls the self-renewal and differentiation of the cells is not well understood. Herein, we report that FGF signaling is essential for self-renewal and the prevention of cell differentiation of DESCs in the CL as well as in DESC spheres. Inhibiting the FGF signaling pathway decreased proliferation and increased apoptosis of the cells in DESC spheres. Suppressing FGFR or its downstream signal transduction pathways diminished Lgr5-expressing cells in the CL and promoted cell differentiation both in DESC spheres and the CL. Furthermore, disruption of the FGF pathway abrogated Wnt signaling to promote Lgr5 expression in DESCs both in vitro and in vivo. This study sheds new light on understanding the mechanism by which the homeostasis, expansion, and differentiation of DESCs are regulated.

Indexed as

Signal TransductionAnimalsCell CycleCell DifferentiationCell ProliferationEpithelial CellsFibroblast Growth FactorsMAP Kinase Signaling SystemMicePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptors, Fibroblast Growth FactorReceptors, G-Protein-CoupledSpheroids, CellularStem CellsToothFibroblast Growth FactorsLgr5 protein, mousePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptors, Fibroblast Growth FactorReceptors, G-Protein-CoupledWnt ProteinsDevelopmentFibroblast Growth Factor (FGF)Fibroblast Growth Factor Receptor (FGFR)Stem CellsToothWnt Signaling

Identifiers

PMID23979135
PMCPMC3789993
OpenAlexW2050828394

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.