Evidence map›Paper›PMID 23741496›Full record

ArticlePloS one2013

Altered expression of ZnT10 in Alzheimer's disease brain.

Helen J Bosomworth, Paul A Adlard, Dianne Ford, Ruth A Valentine

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

29 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. The ZIP3 Zinc Transporter Is Localized to Mossy Fiber Terminals and Is Required for Kainate-Induced Degeneration of CA3 Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Transmembrane 163 (TMEM163) protein effluxes zinc.Archives of biochemistry and biophysics · 2019
    Article
  14. Zinc transporter 10 (ZnT10)-dependent extrusion of cellular MnThe Journal of biological chemistry · 2019
    Article
  15. A structural overview of the zinc transporters in the cation diffusion facilitator family.Acta crystallographica. Section D, Structural biology · 2019
    Review
  16. Review
  17. Zinc Transporter Proteins.Neurochemical research · 2018
    Review
  18. 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

4 authors at 2 institutions in 2 countries.

Helen J BosomworthHuman Nutrition Research Centre, Newcastle University, Newcastle upon Tyne, United Kingdom.
Paul A Adlard
Dianne Ford
Ruth A Valentine
Newcastle University · GBUniversity of Melbourne · AU

Funding

Biotechnology and Biological Sciences Research Council BB/D01669X/1Biotechnology and Biological Sciences Research Council BBD01669X/2Biotechnology and Biological Sciences Research Council BB/F019637/1Medical Research Council G0400074Medical Research Council G0502157Medical Research Council G0900652Medical Research Council G1100540Medical Research Council MR/L016451/1
6 · The paper itself

Abstract

There is an increasing body of evidence suggesting that metal homeostasis is dysregulated in the pathology of Alzheimer's disease (AD). Although expression levels of several transporters belonging the SLC30 family, which comprises predominantly zinc transporters, have been studied in the AD brain, SLC30A10 (ZnT10) has not been studied in this context. To determine if dysregulated expression of ZnT10, which may transport both Zn and Mn, could be a factor that contributes to AD, we investigated if there were differences in ZnT10 mRNA levels in specimens of frontal cortex from AD patients and controls and also if brain tissue from the APP/PS1 transgenic (Tg) mouse model showed abnormal levels of ZnT10 mRNA expression. Our results show that ZnT10 is significantly (P<0.01) decreased in the frontal cortex in AD. Furthermore, we observed a significant decrease in ZnT10 mRNA levels in the APP/PS1-Tg mice compared with wild-type controls (P<0.01). Our results suggest that this dysregulation in ZnT10 could further contribute to disease progression.

Indexed as

Gene Expression RegulationAlzheimer DiseaseAnimalsBrainCation Transport ProteinsDisease ProgressionFemaleFrontal LobeHumansMaleMiceMice, TransgenicRNA, MessengerZinc Transporter 8Cation Transport ProteinsRNA, MessengerSLC30A8 protein, humanZinc Transporter 8

Identifiers

PMID23741496
PMCPMC3669266
OpenAlexW2166501285

What OpenQuestion holds

Textmetadata
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.