Evidence map›Paper›PMID 23857777›Full record

ArticleEMBO molecular medicine2013

A novel epigenetic CREB-miR-373 axis mediates ZIP4-induced pancreatic cancer growth.

Yuqing Zhang, Jingxuan Yang, Xiaobo Cui, Yong Chen, Vivian F Zhu, John P Hagan, Huamin Wang, Xianjun Yu, Sally E Hodges, Jing Fang and 8 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

72 citing papers in PubMed, 102 citations in OpenAlex.

  1. Review
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  11. Multi-faceted regulation of CREB family transcription factors.Frontiers in molecular neuroscience · 2024
    Review
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12 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

18 authors at 7 institutions in 2 countries.

Yuqing ZhangMichael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX, USA.
Jingxuan Yang
Xiaobo Cui
Yong Chen
Vivian F Zhu
John P Hagan
Huamin Wang
Xianjun Yu
Sally E Hodges
Jing Fang
Paul J Chiao
Craig D Logsdon
William E Fisher
F Charles Brunicardi
Changyi Chen
Qizhi Yao
Martin E Fernandez-Zapico
Min Li
Baylor College of Medicine · USThe University of Texas MD Anderson Cancer Center · USChinese Academy of Sciences · CNFudan University Shanghai Cancer Center · CNMayo Clinic · USThe University of Texas Health Science Center at Houston · USUniversity of California, Los Angeles · US

Funding

Tissue CoreP50CA102701 · NCI · MAYO CLINIC ROCHESTER · PI PETERSEN, GLORIA M. · 2004 to 2018
$32.7M
PILOT AND FEASIBILTY PROGRAMP30DK084567 · NIDDK · MAYO CLINIC ROCHESTER · PI GREGORY J. GORES · 2009 to 2026
$22.2M
Role of Dietary Zinc Transporter ZIP4 in Pancreatic CancerR01CA138701 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI LI, MIN · 2010 to 2015
$1.5M
Roles of Zinc Transporter ZIP4 (SLC39A4) in Pancreatic Cancer PathogenesisR21CA133604 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI LI, MIN · 2009 to 2010
$367k
NCI NIH HHS P50 CA102701NCI NIH HHS R01 CA138701NCI NIH HHS R01CA138701NCI NIH HHS R21 CA133604NCI NIH HHS R21CA133604NIDDK NIH HHS P30 DK084567NIDDK NIH HHS P30 DK84567
6 · The paper itself

Abstract

Changes in the intracellular levels of the essential micronutrient zinc have been implicated in multiple diseases including pancreatic cancer; however, the molecular mechanism is poorly understood. Here, we report a novel mechanism where increased zinc mediated by the zinc importer ZIP4 transcriptionally induces miR-373 in pancreatic cancer to promote tumour growth. Reporter, expression and chromatin immunoprecipitation assays demonstrate that ZIP4 activates the zinc-dependent transcription factor CREB and requires this transcription factor to increase miR-373 expression through the regulation of its promoter. miR-373 induction is necessary for efficient ZIP4-dependent enhancement of cell proliferation, invasion, and tumour growth. Further analysis of miR-373 in vivo oncogenic function reveals that it is mediated through its negative regulation of TP53INP1, LATS2 and CD44. These results define a novel ZIP4-CREB-miR-373 signalling axis promoting pancreatic cancer growth, providing mechanistic insights explaining in part how a zinc transporter functions in cancer cells and may have broader implications as inappropriate regulation of intracellular zinc levels plays an important role in many other diseases.

Indexed as

Epigenesis, GeneticAnimalsCation Transport ProteinsCell MovementCell ProliferationCells, CulturedChromatin ImmunoprecipitationCyclic AMP Response Element-Binding ProteinDisease Models, AnimalGene Expression RegulationGenes, ReporterHeterograftsHumansMiceMicroRNAsPancreatic NeoplasmsCation Transport ProteinsCREB1 protein, humanCyclic AMP Response Element-Binding ProteinMicroRNAsMIRN373 microRNA, humanSLC39A4 protein, humanZincmicroRNA-373pancreatic cancerzincZIP4

Identifiers

PMID23857777
PMCPMC3799489
OpenAlexW2131104906

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.