Evidence map›Paper›PMID 26674421›Full record

ReviewInternational journal of oral science2015

Histone methyltransferases and demethylases: regulators in balancing osteogenic and adipogenic differentiation of mesenchymal stem cells.

Peng Deng, Qian-Ming Chen, Christine Hong, Cun-Yu Wang

Open access · goldAbstract readReview
In one paragraph

Review in International journal of oral science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 91 citations in OpenAlex.

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  17. The NCell death & disease · 2021
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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

4 authors at 3 institutions in 2 countries.

Peng DengDivision of Oral Biology and Medicine, School of Dentistry, University of California at Los Angeles, Los Angeles, USA.
Qian-Ming ChenState Key Laboratory of Oral Disease, West China School of Stomatology, Sichuan University, Chengdu, China.
Christine HongSection of Orthodontics, School of Dentistry, University of California at Los Angeles, Los Angeles, USA.
Cun-Yu WangDivision of Oral Biology and Medicine, School of Dentistry, University of California at Los Angeles, Los Angeles, USA.
University of California, Los Angeles · USSamueli Institute · USSichuan University · CN

Funding

Molecular Regulation of Human Dental Stem Cell PropertyR01DE016513 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WANG, CUN-YU · 2005 to 2019
$6.0M
Wnt-4 inhibits peridontitis by attenuating NF-kBR01DE019412 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WANG, CUN-YU · 2008 to 2021
$5.7M
Molecular Control of MSC differentiation and Bone Formation by KDM4BR01AR063089 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WANG, CUN-YU · 2013 to 2017
$1.6M
Promoting DMSC-mediated craniofacial regeneration by estrogenK08DE024603 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HONG, CHRISTINE · 2014 to 2018
$666k
NIAMS NIH HHS R01 AR063089NIDCR NIH HHS DE01651NIDCR NIH HHS DE019412NIDCR NIH HHS K08 DE024603NIDCR NIH HHS K08DE024603-02NIDCR NIH HHS R01 DE016513NIDCR NIH HHS R01 DE019412
6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) are characterized by their self-renewing capacity and differentiation potential into multiple tissues. Thus, management of the differentiation capacities of MSCs is important for MSC-based regenerative medicine, such as craniofacial bone regeneration, and in new treatments for metabolic bone diseases, such as osteoporosis. In recent years, histone modification has been a growing topic in the field of MSC lineage specification, in which the Su(var)3-9, enhancer-of-zeste, trithorax (SET) domain-containing family and the Jumonji C (JmjC) domain-containing family represent the major histone lysine methyltransferases (KMTs) and histone lysine demethylases (KDMs), respectively. In this review, we summarize the current understanding of the epigenetic mechanisms by which SET domain-containing KMTs and JmjC domain-containing KDMs balance the osteogenic and adipogenic differentiation of MSCs.

Indexed as

AdipogenesisCell DifferentiationCell LineageEpigenesis, GeneticF-Box ProteinsHistone DemethylasesHistone-Lysine N-MethyltransferaseHistone MethyltransferasesHumansJumonji Domain-Containing Histone DemethylasesMesenchymal Stem CellsMethyltransferasesOsteogenesisF-Box ProteinsHistone DemethylasesHistone-Lysine N-MethyltransferaseHistone MethyltransferasesJumonji Domain-Containing Histone DemethylasesKDM2A protein, humanMethyltransferasesSU(VAR)3-9

Identifiers

PMID26674421
PMCPMC5153596
OpenAlexW2213096776

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.