Evidence map›Paper›PMID 30781350›Full record

ReviewNutrients2019

Targeting the Zinc Transporter ZIP7 in the Treatment of Insulin Resistance and Type 2 Diabetes.

John Adulcikas, Sabrina Sonda, Shaghayegh Norouzi, Sukhwinder Singh Sohal, Stephen Myers

Open access · goldAbstract readReview
In one paragraph

Review in Nutrients, 2019. 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
3.0field-weighted citation impact, top 10% 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, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. British journal of biomedical science · 2023
    Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Zinc.Advances in food and nutrition research · 2021
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. 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

5 authors at 1 institution in 1 country.

John AdulcikasCollege of Health and Medicine, School of Health Sciences, University of Tasmania, TAS 7005, Australia. johna6@utas.edu.au.
Sabrina SondaCollege of Health and Medicine, School of Health Sciences, University of Tasmania, TAS 7005, Australia. sabrina.sonda@utas.edu.au.
Shaghayegh NorouziCollege of Health and Medicine, School of Health Sciences, University of Tasmania, TAS 7005, Australia. shaghayeg.norouzi@utas.edu.au.
Sukhwinder Singh SohalCollege of Health and Medicine, School of Health Sciences, University of Tasmania, TAS 7005, Australia. sukhwinder.sohal@utas.edu.au.
Stephen MyersCollege of Health and Medicine, School of Health Sciences, University of Tasmania, TAS 7005, Australia. Stephen.myers@utas.edu.au.ORCID 0000-0003-4793-3820
University of Tasmania · AU

Funding

Clifford Graig Medical Research Trust Grant 172
6 · The paper itself

Abstract

Type 2 diabetes mellitus (T2DM) is a disease associated with dysfunctional metabolic processes that lead to abnormally high levels of blood glucose. Preceding the development of T2DM is insulin resistance (IR), a disorder associated with suppressed or delayed responses to insulin. The effects of this response are predominately mediated through aberrant cell signalling processes and compromised glucose uptake into peripheral tissue including adipose, liver and skeletal muscle. Moreover, a major factor considered to be the cause of IR is endoplasmic reticulum (ER) stress. This subcellular organelle plays a pivotal role in protein folding and processes that increase ER stress, leads to maladaptive responses that result in cell death. Recently, zinc and the proteins that transport this metal ion have been implicated in the ER stress response. Specifically, the ER-specific zinc transporter ZIP7, coined the "gate-keeper" of zinc release from the ER into the cytosol, was shown to be essential for maintaining ER homeostasis in intestinal epithelium and myeloid leukaemia cells. Moreover, ZIP7 controls essential cell signalling pathways similar to insulin and activates glucose uptake in skeletal muscle. Accordingly, ZIP7 may be essential for the control of ER localized zinc and mechanisms that disrupt this process may lead to ER-stress and contribute to IR. Accordingly, understanding the mechanisms of ZIP7 action in the context of IR may provide opportunities to develop novel therapeutic options to target this transporter in the treatment of IR and subsequent T2DM.

Indexed as

Cation Transport ProteinsDiabetes Mellitus, Type 2Endoplasmic Reticulum StressHumansInsulin ResistanceSignal TransductionZincCation Transport ProteinsSLC39A7 protein, humanZincendoplasmic reticulum stressinsulin resistancetype 2 diabeteszinczinc transportersZIP7

Identifiers

PMID30781350
PMCPMC6412268
OpenAlexW2914092144

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.