Evidence map›Paper›PMID 22844580›Full record

ArticleScientific reports2012

Altered death receptor signaling promotes epithelial-to-mesenchymal transition and acquired chemoresistance.

James W Antoon, Rongye Lai, Amanda P Struckhoff, Ashley M Nitschke, Steven Elliott, Elizabeth C Martin, Lyndsay V Rhodes, Nam Seung Yoon, Virgilio A Salvo, Bin Shan and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. PET Imaging of Hepatocellular Carcinoma Using ZD2-(Journal of hepatocellular carcinoma · 2023
    Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. EMT signaling: potential contribution of CRISPR/Cas gene editing.Cellular and molecular life sciences : CMLS · 2020
    Review
  16. Review
  17. Article
  18. Review
  19. The role of TNF-α in chordoma progression and inflammatory pathways.Cellular oncology (Dordrecht, Netherlands) · 2019
    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

13 authors at 3 institutions in 1 country.

James W AntoonDepartments of Pharmacology, Tulane University School of Medicine, Tulane Avenue, New Orleans, LA, USA.
Rongye Lai
Amanda P Struckhoff
Ashley M Nitschke
Steven Elliott
Elizabeth C Martin
Lyndsay V Rhodes
Nam Seung Yoon
Virgilio A Salvo
Bin Shan
Barbara S Beckman
Kenneth P Nephew
Matthew E Burow
Tulane University · USIndiana University School of MedicineIndiana University Bloomington · US

Funding

Predicting Drug Resistance in Cancer Genomes by DMA Methylation ProfilingU54CA113001 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HUANG, TIM H.-M. · 2004 to 2014
$16.1M
MEK5-Erk5 in breast cancer resistanceR01CA125806 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI BUROW, MATTHEW E. · 2010 to 2014
$1.5M
NCI NIH HHS CA125806NCI NIH HHS R01 CA125806NCI NIH HHS U54 CA113001
6 · The paper itself

Abstract

Altered death receptor signaling and resistance to subsequent apoptosis is an important clinical resistance mechanism. Here, we investigated the role of death receptor resistance in breast cancer progression. Resistance of the estrogen receptor alpha (ER)-positive, chemosensitive MCF7 breast cancer cell line to tumor necrosis factor (TNF) was associated with loss of ER expression and a multi-drug resistant phenotype. Changes in three major pathways were involved in this transition to a multidrug resistance phenotype: ER, Death Receptor and epithelial to mesenchymal transition (EMT). Resistant cells exhibited altered ER signaling, resulting in decreased ER target gene expression. The death receptor pathway was significantly altered, blocking extrinsic apoptosis and increasing NF-kappaB survival signaling. TNF resistance promoted EMT changes, resulting in a more aggressive phenotype. This first report identifying specific mechanisms underlying acquired resistance to TNF could lead to a better understanding of the progression of breast cancer in response to chemotherapy treatment.

Indexed as

Drug Resistance, NeoplasmSignal TransductionAnimalsApoptosisBreast NeoplasmsCell Line, TumorCell SurvivalCell Transformation, NeoplasticCluster AnalysisDisease Models, AnimalEpithelial-Mesenchymal TransitionEstrogen Receptor alphaFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansEstrogen Receptor alphaNF-kappa BReceptors, Death DomainReceptors, Tumor Necrosis FactorTumor Necrosis Factor-alpha

Identifiers

PMID22844580
PMCPMC3406343
OpenAlexW2044972398

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.