Evidence map›Paper›PMID 24457910›Full record

ArticleScientific reports2014

Epigenetic silencing of ARRDC3 expression in basal-like breast cancer cells.

Young Hwa Soung, Kevin Pruitt, Jun Chung

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

37 citing papers in PubMed, 55 citations in OpenAlex.

  1. A Phase II Study of the Efficacy and Safety of Oral Selinexor in Recurrent Glioblastoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Trial
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  6. Landscape of NcRNAs involved in drug resistance of breast cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  7. Article
  8. Review
  9. Thioredoxin-Interacting Protein in Cancer and Diabetes.Antioxidants & redox signaling · 2022
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  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

3 authors at 1 institution in 1 country.

Young Hwa SoungDepartment of Physiology and Stephenson cancer center, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104.
Kevin PruittDepartment of Molecular and Cellular Physiology Louisiana State University Health Science Center Shreveport, Louisiana 71130.
Jun ChungDepartment of Physiology and Stephenson cancer center, The University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104.
Louisiana State University Health Sciences Center Shreveport · US

Funding

ARRDC3-Integrin beta4 pathway as a therapeutic target of basal-like breast cancerR01CA163657 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI CHUNG, JUN · 2013 to 2017
$1.6M
Mechanisms of Epigenetic Gene SilencingR01CA155223 · NCI · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI PRUITT, KEVIN · 2011 to 2015
$1.4M
NCI NIH HHS 5 R01 CA155223-02NCI NIH HHS R01 CA155223NCI NIH HHS R01 CA163657NCI NIH HHS R01CA163657-01A1
6 · The paper itself

Abstract

Arrestin domain-containing 3 (ARRDC3) is a tumor suppressor whose expression is either lost or suppressed in basal-like breast cancer (BLBC). However, the mechanism by which BLBC suppresses ARRDC3 expression is not established. Here, we show that expression of ARRDC3 in BLBC cells is suppressed at the transcriptional level. Suppression of ARRDC3 expression in BLBC cells involves epigenetic silencing as inhibitors of class III histone deacetylases (HDACs) significantly restores ARRDC3 levels in BLBC cells. SIRT2, among class III HDACs, plays a major role in epigenetic silencing of ARRDC3 in MDA-MB-231 cells. Acetylation levels of the ARRDC3 promoter in BLBC cells is significantly lower than that of other sub-types of BC cells. Chromatin immunopreciptitation analysis established SIRT2 binding at ARRDC3 promoter in BLBC cells. Our studies indicate that SIRT2 dependent epigenetic silencing of ARRDC3 is one of the important events that may contribute to the aggressive nature of BLBC cells.

Indexed as

Epigenesis, GeneticAcetylationApoptosisArrestinsBasal Cell CarcinomaBlotting, WesternBreast NeoplasmsCell MovementCell ProliferationChromatin ImmunoprecipitationFemaleGene Expression Regulation, NeoplasticHistone Deacetylase InhibitorsHistone DeacetylasesHumansPromoter Regions, GeneticARRDC3 protein, humanArrestinsHistone Deacetylase InhibitorsHistone DeacetylasesRNA, Messenger

Identifiers

PMID24457910
PMCPMC3900932
OpenAlexW1982600891

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.