Evidence map›Paper›PMID 27113904›Full record

ArticleScientific reports2016

MiR-142-3p is a RANKL-dependent inducer of cell death in osteoclasts.

Jezrom B Fordham, Katherine Guilfoyle, Afsar Raza Naqvi, Salvador Nares

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 18% 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

19 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Article
  3. Regulation of osteoclast-mediated bone resorption by microRNA.Cellular and molecular life sciences : CMLS · 2022
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. IL-10 Dampens an IL-17-Mediated Periodontitis-Associated Inflammatory Network.Journal of immunology (Baltimore, Md. : 1950) · 2020
    Article
  9. Roles of MicroRNAs in Bone Destruction of Rheumatoid Arthritis.Frontiers in cell and developmental biology · 2020
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
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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 2 institutions in 1 country.

Jezrom B FordhamDepartment of Periodontics, University of Illinois at Chicago, Chicago, Illinois, USA.
Katherine GuilfoyleUniversity of North Carolina at Chapel Hill, School of Dentistry, Department of Periodontics, 385 S. Columbia St., Chapel Hill, NC, 27599, USA.
Afsar Raza NaqviDepartment of Periodontics, University of Illinois at Chicago, Chicago, Illinois, USA.
Salvador NaresDepartment of Periodontics, University of Illinois at Chicago, Chicago, Illinois, USA.
University of Illinois Chicago · USUniversity of North Carolina at Chapel Hill · US

Funding

Functional Modulation of Myeloid Inflammatory Cells by miRNAR01DE021052 · NIDCR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI NARES, SALVADOR · 2011 to 2015
$1.9M
NIDCR NIH HHS R01 DE021052
6 · The paper itself

Abstract

MicroRNA are small, non-coding, single-stranded RNAs that are estimated to regulate ~60% of the human genome. MiRNA profiling of monocyte-to-osteoclast differentiation identified miR-142-3p as a miRNA that is significantly, differentially expressed throughout osteoclastogenesis. Enforced expression of miR-142-3p via transient transfection with miR-142-3p mimic inhibited cell-to-cell contact and fusion, decreased protein kinase C alpha expression, and ultimately reduced cell viability. miR-142-3p was also identified as significantly differentially expressed during monocyte-to-macrophage differentiation and overexpression of miR-142-3p prevented their conversion to osteoclasts. Furthermore, the inhibitory effect of miR-142-3p on osteoclastogenesis extended to the conversion of a third osteoclast precursor cell type- dendritic cells. These results demonstrate miR-142-3p to be a negative regulator of osteoclastogenesis from the 3 main precursor cell types: monocytes, macrophages and dendritic cells. Importantly, decreased survival was dependent upon both miR-142-3p expression and RANK-signaling, with no harmful effects detected in the absence of this combination. As such, miR-142-3p represents a novel target for the selective removal of osteoclasts by targeting of osteoclastogenic pathways.

Indexed as

Cell CommunicationCell DifferentiationCell ProliferationCells, CulturedCell SurvivalDendritic CellsDown-RegulationGene Expression ProfilingHumansMacrophagesMicroRNAsMonocytesOsteoclastsOsteogenesisProtein Kinase C-alphaRANK LigandMicroRNAsMIRN142 microRNA, humanPRKCA protein, humanProtein Kinase C-alphaRANK LigandTNFSF11 protein, human

Identifiers

PMID27113904
PMCPMC4844978
OpenAlexW2343460714

What OpenQuestion holds

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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.