Evidence map›Paper›PMID 30959867›Full record

ReviewMolecules (Basel, Switzerland)2019

Regulation of Osteoclast Differentiation and Skeletal Maintenance by Histone Deacetylases.

Bora Faulkner, Kristina Astleford, Kim C Mansky

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

27 citing papers in PubMed, 41 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Bora FaulknerDepartment of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN 55455, USA. kuyom001@umn.edu.
Kristina AstlefordDiagnostic and Biological Sciences, School of Dentistry, University of Minnesota, Minneapolis, MN 55455, USA. astl0008@umn.edu.
Kim C ManskyDepartment of Developmental and Surgical Sciences, University of Minnesota, Minneapolis, MN 55455, USA. kmansky@umn.edu.ORCID 0000-0002-2826-5030
University of Minnesota · US

Funding

Minnesota Craniofacial Research Training ProgramT90DE022732 · NIDCR · UNIVERSITY OF MINNESOTA · PI MANSKY, KIM CARPENTER · 2012 to 2023
$4.9M
Musculoskeletal Training GrantT32AR050938 · NIAMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI CLOHISY, DENIS R · 2004 to 2020
$3.0M
Role of HDAC7 in Osteoclast DifferentiationR01AR061352 · NIAMS · UNIVERSITY OF MINNESOTA · PI JENSEN, ERIC D, MANSKY, KIM CARPENTER · 2013 to 2017
$1.8M
NIAMS NIH HHS AR061352NIAMS NIH HHS T32 AR050938NIAMS NIH HHS T32AR050938NIDCR NIH HHS T90DE022732
6 · The paper itself

Abstract

Bone is a dynamic tissue that must respond to developmental, repair, and remodeling cues in a rapid manner with changes in gene expression. Carefully-coordinated cycles of bone resorption and formation are essential for healthy skeletal growth and maintenance. Osteoclasts are large, multinucleated cells that are responsible for breaking down bone by secreting acids to dissolve the bone mineral and proteolytic enzymes that degrade the bone extracellular matrix. Increased osteoclast activity has a severe impact on skeletal health, and therefore, osteoclasts represent an important therapeutic target in skeletal diseases, such as osteoporosis. Progression from multipotent progenitors into specialized, terminally-differentiated cells involves carefully-regulated patterns of gene expression to control lineage specification and emergence of the cellular phenotype. This process requires coordinated action of transcription factors with co-activators and co-repressors to bring about proper activation and inhibition of gene expression. Histone deacetylases (HDACs) are an important group of transcriptional co-repressors best known for reducing gene expression via removal of acetyl modifications from histones at HDAC target genes. This review will cover the progress that has been made recently to understand the role of HDACs and their targets in regulating osteoclast differentiation and activity and, thus, serve as potential therapeutic target.

Indexed as

Cell DifferentiationAnimalsBone and BonesBone ResorptionGene Expression RegulationHistone Deacetylase InhibitorsHistone DeacetylasesHumansOsteoclastsTranscription, GeneticHistone Deacetylase InhibitorsHistone Deacetylasesacetylationdifferentiation and resorptiongeneHDACosteoclaststranscription

Identifiers

PMID30959867
PMCPMC6479495
OpenAlexW2933489034

What OpenQuestion holds

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LicenceCC BY
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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.