Evidence map›Paper›PMID 24334408›Full record

ArticleJournal of dental research2014

Vitamin D represses dentin matrix protein 1 in cementoblasts and osteocytes.

F H Nociti, B L Foster, A B Tran, D Dunn, R B Presland, L Wang, N Bhattacharyya, M T Collins, M J Somerman

Abstract read
In one paragraph

Article in Journal of dental research, 2014. 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
2.1field-weighted citation impact, top 14% 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, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Biology of Fibroblast Growth Factor 23: From Physiology to Pathology.Cold Spring Harbor perspectives in medicine · 2018
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. PTH and Vitamin D Repress DMP1 in Cementoblasts.Journal of dental research · 2015
    Article
  14. Article
  15. Article
  16. Mathematical model for bone mineralization.Frontiers in cell and developmental biology · 2015
    Article
  17. Article
  18. Evaluation of Relationship between Body Mass Index withInternational journal of fertility & sterility
    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

9 authors at 4 institutions in 2 countries.

F H NocitiNational Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, USA.
B L Foster
A B Tran
D Dunn
R B Presland
L Wang
N Bhattacharyya
M T Collins
M J Somerman
National Institutes of Health · USNational Institute of Arthritis and Musculoskeletal and Skin Diseases · USUniversity of Washington · USNational Institute of Dental and Craniofacial Research · US

Funding

Skeletal Disorders and Mineral Homeostasis SectionZIADE000649 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI COLLINS, MICHAEL · 2009 to 2025
$32.8M
Laboratory of Oral Connective Tissue BiologyZIAAR041196 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI SOMERMAN, MARTHA · 2013 to 2021
$8.9M
Intramural NIH HHS
6 · The paper itself

Abstract

Calcium and phosphorus homeostasis is achieved by interplay among hormones, including 1,25(OH)2D3 (1,25D), parathyroid hormone, and fibroblast growth factor 23 (FGF23), and their interactions with other proteins. For example, mutations in dentin matrix protein 1 (DMP-1) result in increased FGF23 and hypophosphatemic rickets. 1,25D is reported to modulate FGF23; thus, we hypothesized that 1,25D may be involved in modulating DMP-1 in an intermediary step. Murine cementoblasts (OCCM-30) and osteocyte-like cells (MLO-Y4 and MLO-A5), known to express DMP-1, were used to analyze effects of 1,25D on DMP-1 expression in vitro. DMP-1 mRNA levels decreased by 50% (p < .05) in the presence of 1,25D in all cell types, while use of a vitamin D receptor (VDR) agonist (EB1089) and antagonist (23S,25S)-DLAM-2P confirmed that VDR pathway activation was required for this response. Further analysis showed that histone deacetylase recruitment was necessary, but neither protein kinase A nor C pathways were required. In conclusion, our results support the hypothesis that 1,25D regulates DMP-1 expression through a VDR-dependent mechanism, possibly contributing to local changes in bone/tooth mineral homeostasis.

Indexed as

AnimalsCalcitriolCalcium-Calmodulin-Dependent Protein KinasesCell LineDental CementumDose-Response Relationship, DrugDown-RegulationEstrenesExtracellular Matrix ProteinsFibroblast Growth Factor-23Fibroblast Growth FactorsFlavonoidsHistone Deacetylase InhibitorsHistone DeacetylasesHydroxamic AcidsIndoles1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-onebisindolylmaleimide ICalcitriolCalcium-Calmodulin-Dependent Protein KinasesDmp1 protein, mouseEstrenesExtracellular Matrix ProteinsFgf23 protein, mouseFibroblast Growth Factor-23Fibroblast Growth FactorsFlavonoidsHistone Deacetylase InhibitorsHistone DeacetylasesHydroxamic AcidsIndolesMaleimidesProtein Kinase CPyrrolidinonesReceptors, CalcitriolseocalcitolType C PhospholipasesVitaminsVorinostatfibroblast growth factor 23osteogenesisphosphate homeostasisphosphate regulating endopeptidase homologSIBLING familyVitamin D receptor

Identifiers

PMID24334408
PMCPMC6728571
OpenAlexW2053797304

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.