Evidence map›Paper›PMID 28665752›Full record

ReviewJournal of dental research2017

Signaling Pathways Critical for Tooth Root Formation.

J Wang, J Q Feng

Open access · greenAbstract readReview
In one paragraph

Review in Journal of dental research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.8field-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

37 citing papers in PubMed, 91 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Loss of Stat3 in Prx1Advanced biology · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Genetic Variants inInternational journal of molecular sciences · 2024
    Article
  9. Article
  10. Review
  11. Bone or Tooth dentin: The TGF-β signaling is the key.International journal of biological sciences · 2024
    Article
  12. Article
  13. Article
  14. Primary failure of tooth eruption: Etiology and management.The Japanese dental science review · 2022
    Review
  15. Review
  16. Review
  17. Article
  18. A Biphasic Feature of Gli1Journal of dental research · 2021
    Article
  19. Review
  20. USP34 regulates tooth root morphogenesis by stabilizing NFIC.International journal of oral science · 2021
    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

2 authors at 1 institution in 1 country.

J Wang1 Biomedical Sciences, Texas A&M College of Dentistry, Dallas, TX, USA.
J Q Feng1 Biomedical Sciences, Texas A&M College of Dentistry, Dallas, TX, USA.
Sichuan University · CN

Funding

Biphasic Roles of OSX-WNT-B-Catenin Signaling Pathway in Tooth Root FormationR01DE025014 · NIDCR · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI FENG, JIAN Q. · 2015 to 2019
$1.8M
Chondrocyte-derived bone cells determine the overall pattern of TMJ condyle and contribute to bone remodelingR01DE025659 · NIDCR · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI RUEST, LOUIS-BRUNO · 2017 to 2021
$1.8M
NIDCR NIH HHS R01 DE025014NIDCR NIH HHS R01 DE025659
6 · The paper itself

Abstract

Tooth is made of an enamel-covered crown and a cementum-covered root. Studies on crown dentin formation have been a major focus in tooth development for several decades. Interestingly, the population prevalence for genetic short root anomaly (SRA) with no apparent defects in crown is close to 1.3%. Furthermore, people with SRA itself are predisposed to root resorption during orthodontic treatment. The discovery of the unique role of Nfic (nuclear factor I C; a transcriptional factor) in controlling root but not crown dentin formation points to a new concept: tooth crown and root have different control mechanisms. Further genetic mechanism studies have identified more key molecules (including Osterix, β-catenin, and sonic hedgehog) that play a critical role in root formation. Extensive studies have also revealed the critical role of Hertwig's epithelial root sheath in tooth root formation. In addition, Wnt10a has recently been found to be linked to multirooted tooth furcation formation. These exciting findings not only fill the critical gaps in our understanding about tooth root formation but will aid future research regarding the identifying factors controlling tooth root size and the generation of a whole "bio-tooth" for therapeutic purposes. This review starts with human SRA and mainly focuses on recent progress on the roles of NFIC-dependent and NFIC-independent signaling pathways in tooth root formation. Finally, this review includes a list of the various Cre transgenic mouse lines used to achieve tooth root formation-related gene deletion or overexpression, as well as strengths and limitations of each line.

Indexed as

Signal TransductionAnimalsbeta CateninDental CementumDentinEnamel OrganHedgehog ProteinsHumansMiceNerve Tissue ProteinsNFI Transcription FactorsOdontogenesisSp7 Transcription FactorTooth RootTranscription FactorsWnt Proteinsbeta CateninHedgehog ProteinsNerve Tissue ProteinsNFI Transcription FactorsSP7 protein, humanSp7 protein, mouseSp7 Transcription FactorTranscription FactorsWNT10A protein, humanWnt10a protein, mouseWnt Proteinscell signalingdentinNFICodontogenesisosterixtooth regeneration

Identifiers

PMID28665752
PMCPMC5613878
OpenAlexW2724386338

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.