Evidence map›Paper›PMID 27274087›Full record

ArticleThe Biochemical journal2016

Zinc transporter ZIP10 forms a heteromer with ZIP6 which regulates embryonic development and cell migration.

Kathryn M Taylor, Issa A Muraina, Dylan Brethour, Gerold Schmitt-Ulms, Thirayost Nimmanon, Silvia Ziliotto, Peter Kille, Christer Hogstrand

Open access · hybridAbstract read
In one paragraph

Article in The Biochemical journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
9.4field-weighted citation impact, top 1% 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

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 119 citations in OpenAlex.

  1. Pooled it
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  8. Reduction in the hepatocellular carcinoma antioncogeneWorld journal of gastrointestinal surgery · 2025
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4 more citing papers are in PubMed but not listed here.

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 4 institutions in 3 countries.

Kathryn M TaylorBreast Cancer Molecular Pharmacology Unit, School of Pharmacy and Pharmaceutical Sciences, Redwood Building, Cardiff University, King Edward VII Avenue, Cardiff CF10 3NB, U.K. TaylorKM@cardiff.ac.uk christer.hogstrand@kcl.ac.uk.
Issa A MurainaKing's College London, Faculty of Life Sciences and Medicine, Diabetes and Nutritional Sciences, Metal Metabolism Group, 150 Stamford St., London SE1 NH9, U.K. National Veterinary Research Institute, PMB 01 Vom, Nigeria.
Dylan BrethourTanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Ontario, Canada M5T 3S8 Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada M5S 3H2.
Gerold Schmitt-UlmsTanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Ontario, Canada M5T 3S8 Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada M5S 3H2.
Thirayost NimmanonBreast Cancer Molecular Pharmacology Unit, School of Pharmacy and Pharmaceutical Sciences, Redwood Building, Cardiff University, King Edward VII Avenue, Cardiff CF10 3NB, U.K. Department of Pathology, Phramongkutklao College of Medicine, 315 Ratchawithi Road, Thung Phayathai, Ratchathewi, Bangkok 10400, Thailand.
Silvia ZiliottoBreast Cancer Molecular Pharmacology Unit, School of Pharmacy and Pharmaceutical Sciences, Redwood Building, Cardiff University, King Edward VII Avenue, Cardiff CF10 3NB, U.K.
Peter KilleSchool of Biosciences, Cardiff University, Sir Martin Evans Building, Museum Avenue, Cardiff CF10 3AT, U.K.
Christer HogstrandKing's College London, Faculty of Life Sciences and Medicine, Diabetes and Nutritional Sciences, Metal Metabolism Group, 150 Stamford St., London SE1 NH9, U.K. TaylorKM@cardiff.ac.uk christer.hogstrand@kcl.ac.uk.
National Veterinary Research Institute · NGOccupational Cancer Research Centre · CAPhramongkutklao College of MedicineUniversity of Toronto · CA

Funding

CIHR 324987Wellcome Trust 091991/Z/10/Z
6 · The paper itself

Abstract

There is growing evidence that zinc and its transporters are involved in cell migration during development and in cancer. In the present study, we show that zinc transporter ZIP10 (SLC39A10) stimulates cell motility and proliferation, both in mammalian cells and in the zebrafish embryo. This is associated with inactivation of GSK (glycogen synthase kinase)-3α and -3β and down-regulation of E-cadherin (CDH1). Morpholino-mediated knockdown of zip10 causes delayed epiboly and deformities of the head, eye, heart and tail. Furthermore, zip10 deficiency results in overexpression of cdh1, zip6 and stat3, the latter gene product driving transcription of both zip6 and zip10 The non-redundant requirement of Zip6 and Zip10 for epithelial to mesenchymal transition (EMT) is consistent with our finding that they exist as a heteromer. We postulate that a subset of ZIPs carrying prion protein (PrP)-like ectodomains, including ZIP6 and ZIP10, are integral to cellular pathways and plasticity programmes, such as EMT.

Indexed as

Cell MovementEmbryonic DevelopmentAnimalsCation Transport ProteinsCell AdhesionCell ProliferationCHO CellsClustered Regularly Interspaced Short Palindromic RepeatsCricetulusEpithelial-Mesenchymal TransitionFemaleHumansMaleMCF-7 CellsPhylogenyZebrafishCation Transport ProteinsZinccancerhumanmouseSLC39A10SLC39A6zebrafish

Identifiers

PMID27274087
PMCPMC4980808
OpenAlexW2412540739

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.