Evidence map›Paper›PMID 35525910›Full record

ArticleInternational journal of oral science2022

Loss of KDM4B impairs osteogenic differentiation of OMSCs and promotes oral bone aging.

Peng Deng, Insoon Chang, Jiongke Wang, Amr A Badreldin, Xiyao Li, Bo Yu, Cun-Yu Wang

Open access · goldAbstract read
In one paragraph

Article in International journal of oral science, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  9. Emerging role of liver-bone axis in osteoporosis.Journal of orthopaedic translation · 2024
    Review
  10. Article
  11. Article
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  16. Gene signature of mScientific reports · 2022
    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

7 authors at 2 institutions in 1 country.

Peng Deng *Laboratory of Molecular Signaling, Division of Oral and Systemic Health Sciences, School of Dentistry, UCLA, Los Angeles, CA, USA.
Insoon Chang *Laboratory of Molecular Signaling, Division of Oral and Systemic Health Sciences, School of Dentistry, UCLA, Los Angeles, CA, USA.
Jiongke WangDivision of Preventive and Restorative Sciences, School of Dentistry, UCLA, Los Angeles, CA, USA.
Amr A BadreldinLaboratory of Molecular Signaling, Division of Oral and Systemic Health Sciences, School of Dentistry, UCLA, Los Angeles, CA, USA.
Xiyao LiLaboratory of Molecular Signaling, Division of Oral and Systemic Health Sciences, School of Dentistry, UCLA, Los Angeles, CA, USA.
Bo YuDivision of Preventive and Restorative Sciences, School of Dentistry, UCLA, Los Angeles, CA, USA.
Cun-Yu WangLaboratory of Molecular Signaling, Division of Oral and Systemic Health Sciences, School of Dentistry, UCLA, Los Angeles, CA, USA. cwang@dentistry.ucla.edu.ORCID 0000-0002-3885-5149
University of California, Los Angeles · USUCLA Health · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Wnt-4 inhibits peridontitis by attenuating NF-kBR01DE019412 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WANG, CUN-YU · 2008 to 2021
$5.7M
Epigenetic Regulation of Orofacial Bone Homeostasis and Aging by KDM4BR01DE028260 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WANG, CUN-YU · 2018 to 2022
$1.8M
NCI NIH HHS P30 CA016042NIDCR NIH HHS R01 DE019412NIDCR NIH HHS R01 DE028260
6 · The paper itself

Abstract

Aging of craniofacial skeleton significantly impairs the repair and regeneration of trauma-induced bony defects, and complicates dental treatment outcomes. Age-related alveolar bone loss could be attributed to decreased progenitor pool through senescence, imbalance in bone metabolism and bone-fat ratio. Mesenchymal stem cells isolated from oral bones (OMSCs) have distinct lineage propensities and characteristics compared to MSCs from long bones, and are more suited for craniofacial regeneration. However, the effect of epigenetic modifications regulating OMSC differentiation and senescence in aging has not yet been investigated. In this study, we found that the histone demethylase KDM4B plays an essential role in regulating the osteogenesis of OMSCs and oral bone aging. Loss of KDM4B in OMSCs leads to inhibition of osteogenesis. Moreover, KDM4B loss promoted adipogenesis and OMSC senescence which further impairs bone-fat balance in the mandible. Together, our data suggest that KDM4B may underpin the molecular mechanisms of OMSC fate determination and alveolar bone homeostasis in skeletal aging, and present as a promising therapeutic target for addressing craniofacial skeletal defects associated with age-related deteriorations.

Indexed as

AgingFacial BonesJumonji Domain-Containing Histone DemethylasesMesenchymal Stem CellsOsteogenesisOsteoporosisCell DifferentiationHumansJumonji Domain-Containing Histone DemethylasesKDM4B protein, human

Identifiers

PMID35525910
PMCPMC9079076
OpenAlexW4228999779

What OpenQuestion holds

Textmetadata
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.