Evidence map›Paper›PMID 27554624›Full record

ArticleScientific reports2016

Dicer ablation in osteoblasts by Runx2 driven cre-loxP recombination affects bone integrity, but not glucocorticoid-induced suppression of bone formation.

Peng Liu, Mario Baumgart, Marco Groth, Jürgen Wittmann, Hans-Martin Jäck, Matthias Platzer, Jan P Tuckermann, Ulrike Baschant

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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 20% 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, 26 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. Article
  6. Review
  7. Regulation and Role of Transcription Factors in Osteogenesis.International journal of molecular sciences · 2021
    Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. The role of microRNAs in glucocorticoid action.The Journal of biological chemistry · 2018
    Review
  16. Regulation of Bone Metabolism by microRNAs.Current osteoporosis reports · 2018
    Review
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

8 authors at 3 institutions in 1 country.

Peng LiuInstitute of Comparative Molecular Endocrinology (CME), Ulm University, Ulm, Germany.
Mario BaumgartLeibniz Institute on Aging- Fritz-Lipmann Institute, Jena, Germany.
Marco GrothLeibniz Institute on Aging- Fritz-Lipmann Institute, Jena, Germany.
Jürgen WittmannDivision of Molecular Immunology, Department of Internal Medicine III, Nikolaus-Fiebiger-Center, University of Erlangen-Nuremberg, Erlangen, Germany.
Hans-Martin JäckDivision of Molecular Immunology, Department of Internal Medicine III, Nikolaus-Fiebiger-Center, University of Erlangen-Nuremberg, Erlangen, Germany.
Matthias PlatzerLeibniz Institute on Aging- Fritz-Lipmann Institute, Jena, Germany.
Jan P TuckermannInstitute of Comparative Molecular Endocrinology (CME), Ulm University, Ulm, Germany.
Ulrike BaschantInstitute of Comparative Molecular Endocrinology (CME), Ulm University, Ulm, Germany.
Leibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEUniversität Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glucocorticoid-induced osteoporosis (GIO) is one of the major side effects of long-term glucocorticoid (GC) therapy mediated mainly via the suppression of bone formation and osteoblast differentiation independently of GC receptor (GR) dimerization. Since microRNAs play a critical role in osteoblast differentiation processes, we investigated the role of Dicer dependent microRNAs in the GC-induced suppression of osteoblast differentiation. MicroRNA sequencing of dexamethasone-treated wild-type and GR dimer-deficient mesenchymal stromal cells revealed GC-controlled miRNA expression in a GR dimer-dependent and GR dimer-independent manner. To determine the functional relevance of mature miRNAs in GC-induced osteoblast suppression, mice with an osteoblast-specific deletion of Dicer (Dicer(Runx2Cre)) were exposed to glucocorticoids. In vitro generated Dicer-deficient osteoblasts were treated with dexamethasone and analyzed for proliferation, differentiation and mineralization capacity. In vivo, abrogation of Dicer-dependent miRNA biogenesis in osteoblasts led to growth retardation and impaired bone formation. However, subjecting these mice to GIO showed that bone formation was similar reduced in Dicer(Runx2Cre) mice and littermate control mice upon GC treatment. In line, differentiation of Dicer deficient osteoblasts was suppressed to the same extent as wild type cells by GC treatment. Therefore, Dicer-dependent small RNA biogenesis in osteoblasts plays only a minor role in the pathogenesis of GC-induced inhibition of bone formation.

Indexed as

AnimalsCell DifferentiationCell ProliferationCore Binding Factor Alpha 1 SubunitDEAD-box RNA HelicasesDexamethasoneFemurGlucocorticoidsIntegrasesMesenchymal Stem CellsMice, KnockoutMice, TransgenicMicroRNAsOsteoblastsOsteogenesisOsteoporosisCore Binding Factor Alpha 1 SubunitCre recombinaseDEAD-box RNA HelicasesDexamethasoneDicer1 protein, mouseGlucocorticoidsIntegrasesMicroRNAsReceptors, GlucocorticoidRibonuclease IIIRunx2 protein, mouse

Identifiers

PMID27554624
PMCPMC4995469
OpenAlexW2516189691

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Registered trials

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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.