Evidence map›Paper›PMID 38555001›Full record

ReviewBiochimica et biophysica acta. Reviews on cancer2024

All eyes on Eya: A unique transcriptional co-activator and phosphatase in cancer.

Connor J Hughes, Christopher Alderman, Arthur R Wolin, Kaiah M Fields, Rui Zhao, Heide L Ford

Open access · greenAbstract readReview
In one paragraph

Review in Biochimica et biophysica acta. Reviews on cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.6field-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

8 citing papers in PubMed, 11 citations in OpenAlex.

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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 1 institution in 1 country.

Connor J HughesMedical Scientist Training Program, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, United States of America; Department of Pharmacology, University of Colorado Anschutz Medical Campus, 12800 East 19th Avenue, Aurora, CO 80045, United States of America.
Christopher AldermanMedical Scientist Training Program, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, United States of America; Molecular Biology Program, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, United States of America; Department of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, United States of America.
Arthur R WolinDepartment of Pharmacology, University of Colorado Anschutz Medical Campus, 12800 East 19th Avenue, Aurora, CO 80045, United States of America; Molecular Biology Program, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, United States of America.
Kaiah M FieldsDepartment of Pharmacology, University of Colorado Anschutz Medical Campus, 12800 East 19th Avenue, Aurora, CO 80045, United States of America; Molecular Biology Program, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, United States of America.
Rui ZhaoMedical Scientist Training Program, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, United States of America; Molecular Biology Program, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, United States of America; Department of Biochemistry and Molecular Genetics, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, United States of America. Electronic address: rui.zhao@cuanschutz.edu.
Heide L FordMedical Scientist Training Program, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, United States of America; Department of Pharmacology, University of Colorado Anschutz Medical Campus, 12800 East 19th Avenue, Aurora, CO 80045, United States of America; Molecular Biology Program, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, United States of America. Electronic address: heide.ford@cuanschutz.edu.
University of Colorado Anschutz Medical Campus · US

Funding

The molecular mechanism of pre-mRNA splicingR35GM145289 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI RUI ZHAO · 2022 to 2026
$4.3M
Training in Translational Research of Lung, Head and Neck CancerT32CA174648 · NCI · UNIVERSITY OF COLORADO DENVER · PI KARAM, SANA D · 2013 to 2022
$4.2M
Deciphering Mechanisms by which Tumor Cells Collaborate to Mediate MetastasisR01CA224867 · NCI · UNIVERSITY OF COLORADO DENVER · PI FORD, HEIDE L., LEWIS, MICHAEL T. · 2019 to 2023
$3.2M
Role of Eya3 in regulating the immune microenvironment to promote breast tumor progressionR01CA221282 · NCI · UNIVERSITY OF COLORADO DENVER · PI FORD, HEIDE L., ZHAO, RUI · 2017 to 2021
$3.2M
Reprogramming myogenic regulatory factors in RMS to promote differentiation and halt growthR01CA275187 · NCI · UNIVERSITY OF COLORADO DENVER · PI Kristin Artinger, Heide L. Ford · 2023 to 2026
$2.8M
Examining the EYA2/MYC axis in Group 3 MedulloblastomaR01NS108396 · NINDS · UNIVERSITY OF COLORADO DENVER · PI FORD, HEIDE L. · 2018 to 2021
$1.6M
Investigating the role of Eya3 in the regulation of innate immune signaling cascades in Triple Negative Breast CancerF30CA257215 · NCI · UNIVERSITY OF COLORADO DENVER · PI HUGHES, CONNOR J · 2021 to 2023
$108k
Elucidating the role of EYA2 at centrosomes in glioblastoma stem cellsF31CA275314 · NCI · UNIVERSITY OF COLORADO DENVER · PI WOLIN, ARTHUR R · 2023 to 2024
$68k
NCI NIH HHS F30 CA257215NCI NIH HHS F31 CA275314NCI NIH HHS R01 CA221282NCI NIH HHS R01 CA224867NCI NIH HHS R01 CA275187NCI NIH HHS T32 CA174648NIGMS NIH HHS R35 GM145289NINDS NIH HHS R01 NS108396
6 · The paper itself

Abstract

The Eya family of proteins (consisting of Eyas1-4 in mammals) play vital roles in embryogenesis by regulating processes such as proliferation, migration/invasion, cellular survival and pluripotency/plasticity of epithelial and mesenchymal states. Eya proteins carry out such diverse functions through a unique combination of transcriptional co-factor, Tyr phosphatase, and PP2A/B55α-mediated Ser/Thr phosphatase activities. Since their initial discovery, re-expression of Eyas has been observed in numerous tumor types, where they are known to promote tumor progression through a combination of their transcriptional and enzymatic activities. Eya proteins thus reinstate developmental processes during malignancy and represent a compelling class of therapeutic targets for inhibiting tumor progression.

Indexed as

NeoplasmsProtein Tyrosine PhosphatasesAnimalsEye ProteinsGene Expression Regulation, NeoplasticHumansIntracellular Signaling Peptides and ProteinsNuclear ProteinsEYA1 protein, humanEYA2 protein, humanEye ProteinsIntracellular Signaling Peptides and ProteinsNuclear ProteinsProtein Tyrosine PhosphatasesEya proteinsMetastasisProtein phosphatase 2ASerine/threonine phosphataseTranscriptional co-factorTyrosine phosphatase

Identifiers

PMID38555001
PMCPMC11111358
OpenAlexW4393282650

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.