Evidence map›Paper›PMID 32046982›Full record

ArticleCancer research2020

ETV4 Is Necessary for Estrogen Signaling and Growth in Endometrial Cancer Cells.

Adriana C Rodriguez, Jeffery M Vahrenkamp, Kristofer C Berrett, Kathleen A Clark, Katrin P Guillen, Sandra D Scherer, Chieh-Hsiang Yang, Bryan E Welm, Margit M Janát-Amsbury, Barbara J Graves and 1 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

47 citing papers in PubMed, 68 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Ferroptosis, Metabolic Rewiring, and Endometrial Cancer.International journal of molecular sciences · 2023
    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

11 authors at 2 institutions in 1 country.

Adriana C RodriguezDepartment of Oncological Sciences, University of Utah, Salt Lake City, Utah.
Jeffery M VahrenkampDepartment of Oncological Sciences, University of Utah, Salt Lake City, Utah.
Kristofer C BerrettDepartment of Oncological Sciences, University of Utah, Salt Lake City, Utah.
Kathleen A ClarkDepartment of Oncological Sciences, University of Utah, Salt Lake City, Utah.
Katrin P GuillenDepartment of Oncological Sciences, University of Utah, Salt Lake City, Utah.
Sandra D SchererDepartment of Oncological Sciences, University of Utah, Salt Lake City, Utah.
Chieh-Hsiang YangHuntsman Cancer Institute, University of Utah, Salt Lake City, Utah.
Bryan E WelmDepartment of Oncological Sciences, University of Utah, Salt Lake City, Utah.
Margit M Janát-AmsburyDivision of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Utah, Salt Lake City, Utah.
Barbara J GravesDepartment of Oncological Sciences, University of Utah, Salt Lake City, Utah.ORCID 0000-0003-0807-5982
Jason GertzDepartment of Oncological Sciences, University of Utah, Salt Lake City, Utah. jay.gertz@hci.utah.edu.
University of Utah · USHoward Hughes Medical Institute · US

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Jared P Rutter · 1986 to 2026
$72.6M
In situ evaluation of combinatorial gene regulation in the human genomeR01HG008974 · NHGRI · UNIVERSITY OF UTAH · PI GERTZ, JASON · 2017 to 2021
$3.2M
Impact of enhancer sequence and interacting factors on estrogen receptor-mediatedR00HG006922 · NHGRI · UNIVERSITY OF UTAH · PI GERTZ, JASON · 2014 to 2016
$811k
NCRR Confocal ProposalS10RR024761 · NCRR · UNIVERSITY OF UTAH · PI RODESCH, CHRISTOPHER K · 2008 to 2008
$475k
Epigenetic Mechanisms of Memories Associated with Cocaine RewardK99DA024761 · NIDA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MILLER, COURTNEY A · 2009 to 2009
$106k
NCI NIH HHS P30 CA042014NCRR NIH HHS S10 RR024761NHGRI NIH HHS R00 HG006922NHGRI NIH HHS R01 HG008974NIDA NIH HHS K99 DA024761
6 · The paper itself

Abstract

Estrogen signaling through estrogen receptor alpha (ER) plays a major role in endometrial cancer risk and progression, however, the molecular mechanisms underlying ER's regulatory role in endometrial cancer are poorly understood. In breast cancer cells, ER genomic binding is enabled by FOXA1 and GATA3, but the transcription factors that control ER genomic binding in endometrial cancer cells remain unknown. We previously identified ETV4 as a candidate factor controlling ER genomic binding in endometrial cancer cells, and here we explore the functional importance of ETV4. Homozygous deletion of ETV4, using CRISPR/Cas9, led to greatly reduced ER binding at the majority of loci normally bound by ER. Consistent with the dramatic loss of ER binding, the gene expression response to estradiol was dampened for most genes. ETV4 contributes to estrogen signaling in two distinct ways. ETV4 loss affects chromatin accessibility at some ER bound loci and impairs ER nuclear translocation. The diminished estrogen signaling upon ETV4 deletion led to decreased growth, particularly in 3D culture, where hollow organoids were formed and

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCell Line, TumorCell NucleusChromatinChromatin Immunoprecipitation SequencingCytoplasmEndometrial NeoplasmsEstradiolEstrogen Receptor alphaFemaleGene Knockout TechniquesHumansMiceProto-Oncogene Proteins c-etsRNA-SeqChromatinESR1 protein, humanEstradiolEstrogen Receptor alphaETV4 protein, humanProto-Oncogene Proteins c-ets

Identifiers

PMID32046982
PMCPMC7073291
OpenAlexW3006318294

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.