Evidence map›Paper›PMID 18976705›Full record

ArticleBiochimica et biophysica acta2009

GALNT3, a gene associated with hyperphosphatemic familial tumoral calcinosis, is transcriptionally regulated by extracellular phosphate and modulates matrix metalloproteinase activity.

Ilana Chefetz, Kimitoshi Kohno, Hiroto Izumi, Jouni Uitto, Gabriele Richard, Eli Sprecher

Open access · greenAbstract read
In one paragraph

Article in Biochimica et biophysica acta, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

28 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. The vitamin DAmerican journal of physiology. Cell physiology · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Effects of ferric citrate and intravenous iron sucrose on markers of mineral, bone, and iron homeostasis in a rat model of CKD-MBD.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Upstream Regulators of Fibroblast Growth Factor 23.Frontiers in endocrinology · 2021
    Review
  12. Mechanisms of phosphate transport.Nature reviews. Nephrology · 2019
    Review
  13. Hyperphosphatemic familial tumoral calcinosis secondary to fibroblast growth factor 23 (FGF23) mutation: a report of two affected families and review of the literature.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2018
    Review
  14. Effect of rosuvastatin on the expression of candidate geneExperimental and therapeutic medicine · 2018
    Article
  15. Article
  16. Article
  17. Skin manifestations in CDG.Journal of inherited metabolic disease · 2014
    Review
  18. Dynamic regulation of FGF23 by Fam20C phosphorylation, GalNAc-T3 glycosylation, and furin proteolysis.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  19. Review
  20. 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

6 authors at 3 institutions in 3 countries.

Ilana ChefetzLaboratory of Molecular Dermatology and Department of Dermatology, Rambam Health Care Campus, Haifa, Israel.
Kimitoshi Kohno
Hiroto Izumi
Jouni Uitto
Gabriele Richard
Eli Sprecher
Technion – Israel Institute of Technology · ILThomas Jefferson University · USUniversity of Occupational and Environmental Health Japan · JP

Funding

Molecular Genetics of Familial Tumoral CalcinosisR01AR052627 · NIAMS · THOMAS JEFFERSON UNIVERSITY · PI UITTO, JOUNI · 2005 to 2009
$1.6M
NIAMS NIH HHS AR05262NIAMS NIH HHS R01 AR052627
6 · The paper itself

Abstract

GALNT3 encodes UDP-N-acetyl-alpha-d-galactosamine: polypeptide N-acetylgalactosaminyl-transferarase 3 (ppGalNacT3), a glycosyltransferase which has been suggested to prevent proteolysis of FGF23, a potent phosphaturic protein. Accordingly, loss-of-function mutations in GALNT3 cause hyperphosphatemic familial tumoral calcinosis (HFTC), a rare autosomal recessive disorder manifesting with increased kidney reabsorption of phosphate, resulting in severe hyperphosphatemia and widespread ectopic calcifications. Although these findings definitely attribute a role to ppGalNacT3 in the regulation of phosphate homeostasis, little is currently known about the factors regulating GALNT3 expression. In addition, the effect of decreased GALNT3 expression in peripheral tissues has not been explored so far. In the present study, we demonstrate that GALNT3 expression is under the regulation of a number of factors known to be associated with phosphate homeostasis, including inorganic phosphate itself, calcium and 1,25-dihydroxyvitamin D(3). In addition, we show that decreased GALNT3 expression in human skin fibroblasts leads to increased expression of FGF7 and of matrix metalloproteinases, which have been previously implicated in the pathogenesis of ectopic calcification. Thus, the present data suggest that ppGalNacT3 may play a role in peripheral tissues of potential relevance to the pathogenesis of disorders of phosphate metabolism.

Indexed as

Base SequenceCalcinosisCells, CulturedDNA PrimersDown-RegulationExtracellular FluidFibroblast Growth Factor-23Fibroblast Growth Factor 7FibroblastsGene Expression Regulation, EnzymologicHumansHyperphosphatemiaMatrix MetalloproteinasesMutationN-AcetylgalactosaminyltransferasesPhosphatesDNA PrimersFGF23 protein, humanFGF7 protein, humanFibroblast Growth Factor-23Fibroblast Growth Factor 7Matrix MetalloproteinasesN-AcetylgalactosaminyltransferasesPhosphatesPolypeptide N-acetylgalactosaminyltransferaseRNA, Small Interfering

Identifiers

PMID18976705
PMCPMC3169302
OpenAlexW2143866090

What OpenQuestion holds

Textmetadata
LicenceTDM
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.