Evidence map›Paper›PMID 30927049›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2019

Fructose 1,6-bisphosphate inhibits osteoclastogenesis by attenuating RANKL-induced NF-κB/NFATc-1.

L Wilches-Buitrago, P R Viacava, F Q Cunha, J C Alves-Filho, S Y Fukada

Abstract read
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In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Glucose metabolism in osteoporosis: A potential therapeutic target (Review).International journal of molecular medicine · 2026
    Review
  2. Review
  3. Review
  4. ARRDC4-mediated glycolysis enhances innate immunity to influenza A virus through fructose-1,6-bisphosphate.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Review
  6. Novel Insights into Osteoclast Energy Metabolism.Current osteoporosis reports · 2023
    Review
  7. The role of lactate in cardiovascular diseases.Cell communication and signaling : CCS · 2023
    Review
  8. Article
  9. Article
  10. Article
  11. [Simvastatin promotes murine osteoclasts apoptosisNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2019
    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

5 authors at 2 institutions in 1 country.

L Wilches-BuitragoRibeirao Preto Medical School, Department of Pharmacology, University of Sao Paulo, Ribeirao Preto, Brazil.
P R ViacavaRibeirao Preto Medical School, Department of Pharmacology, University of Sao Paulo, Ribeirao Preto, Brazil.
F Q CunhaRibeirao Preto Medical School, Department of Pharmacology, University of Sao Paulo, Ribeirao Preto, Brazil.
J C Alves-FilhoRibeirao Preto Medical School, Department of Pharmacology, University of Sao Paulo, Ribeirao Preto, Brazil.
S Y FukadaSchool of Pharmaceutical Sciences of Ribeirao Preto, Department of Physics and Chemistry, University of Sao Paulo, Ribeirao Preto, Brazil. sfukada@usp.br.ORCID http://orcid.org/0000-0002-6589-4784
Universidade de São Paulo · BRUniversidade de Ribeirão Preto · BR

Funding

CNPq 130230/2016-2FAPESP 2013/08216-2FAPESP 2015/09034-0
6 · The paper itself

Abstract

backgroundAlthough some glycolytic intermediates have been shown to modulate several cell type formation and activation, the functional role of fructose 1,6-bisphosphate (FBP) on osteoclastogenesis is still unknown.

methodsOsteoclastogenesis was evaluated on bone marrow preosteoclasts cultured with M-CSF - 30 ng/ml, RANKL - 10 ng/ml, and two concentrations of FBP (100 and 300 µM). TRAP-positive stained cells were counted, and osteoclastogenic marker genes expression were evaluated by qPCR. Osteoclasts resorption capacity was evaluated by the expression of specific enzymes and capacity to resorb a mineralized matrix. The NF-κB activation was detected using RAW 264.7, stably expressing luciferase on the NF-κB responsive promoter.

resultsWe show that FBP, the product of the first stage of glycolysis, inhibited RANKL-induced osteoclasts differentiation and TRAP activity. The treatment of preosteoclasts with FBP attenuated osteoclast fusion and formation, without affecting cell viability. Moreover, the inhibition of several osteoclastogenic marker genes expression (TRAP, OSCAR, DC-STAMP, Integrin αv, NFATc1) by FBP correlates with a reduction of mineralized matrix resorption capacity. The mechanism underlying FBP-inhibition of osteoclastogenesis involves NF-κB/NFATc1 signaling pathway inhibition.

conclusionAltogether these data show a protective role of a natural glycolytic intermediate in bone homeostasis that may have therapeutic benefit for osteolytic diseases.

Indexed as

AnimalsBone Marrow CellsCell DifferentiationCells, CulturedFemurFructosediphosphatesMaleMice, Inbred C57BLNFATC Transcription FactorsNF-kappa BOsteoclastsOsteogenesisRANK LigandTibiafructose-1,6-diphosphateFructosediphosphatesNfatc1 protein, mouseNFATC Transcription FactorsNF-kappa BRANK LigandBone remodelingFructose 1,6-bisphosphateNFATc1Osteoclasts

Identifiers

PMID30927049
OpenAlexW2926189780

What OpenQuestion holds

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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.