Evidence map›Paper›PMID 21170267›Full record

ArticleNeoplasia (New York, N.Y.)2010

ERG cooperates with androgen receptor in regulating trefoil factor 3 in prostate cancer disease progression.

David S Rickman, Ying-Bei Chen, Samprit Banerjee, Yihang Pan, Jindan Yu, Terry Vuong, Sven Perner, Christopher J Lafargue, Kirsten D Mertz, Sunita R Setlur and 5 more

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
6.7field-weighted citation impact, top 3% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Genome-Based Classification and Therapy of Prostate Cancer.Diagnostics (Basel, Switzerland) · 2018
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. ERG/AKR1C3/AR Constitutes a Feed-Forward Loop for AR Signaling in Prostate Cancer Cells.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    Article
  16. Article
  17. Article
  18. Article
  19. 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

15 authors at 6 institutions in 3 countries.

David S RickmanDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY 10065, USA.
Ying-Bei Chen
Samprit Banerjee
Yihang Pan
Jindan Yu
Terry Vuong
Sven Perner
Christopher J Lafargue
Kirsten D Mertz
Sunita R Setlur
Kanishka Sircar
Arul M Chinnaiyan
Tarek A Bismar
Mark A Rubin
Francesca Demichelis
Cornell University · USHarvard University Press · USUniversity of Michigan–Ann Arbor · USThe University of Texas MD Anderson Cancer Center · USUniversity Hospital of Zurich · CHUniversity of Calgary · CA

Funding

Towards Understanding Prostate Cancer HeterogeneityR01CA125612 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI RUBIN, MARK A. · 2007 to 2017
$3.4M
Mechanistic Insights Underlying ERG-induced Taxane Resistance in Castration-ResisR01CA179100 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI GIANNAKAKOU, PARASKEVI, RICKMAN, DAVID S. · 2014 to 2018
$2.1M
The Role of beta-adrenergic Signaling in Prostate CancerR00CA129565 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI YU, JINDAN · 2010 to 2012
$732k
The Role of beta-adrenergic Signaling in Prostate CancerK99CA129565 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI YU, JINDAN · 2008 to 2009
$310k
NCI NIH HHS K99 CA129565NCI NIH HHS R00 CA129565NCI NIH HHS R01 CA125612NCI NIH HHS R01 CA125612-01NCI NIH HHS R01 CA179100
6 · The paper itself

Abstract

To elucidate the role of ETS gene fusions in castration-resistant prostate cancer (CRPC), we characterized the transcriptome of 54 CRPC tumor samples from men with locally advanced or metastatic disease. Trefoil factor 3 (TFF3) emerged as the most highly differentially regulated gene with respect to ERG rearrangement status and resistance to hormone ablation therapy. Conventional chromatin immunoprecipitation (ChIP)-polymerase chain reaction and ChIP followed by DNA sequencing (ChIP-seq) revealed direct binding of ERG to ETS binding sites in the TFF3 promoter in ERG-rearranged prostate cancer cell lines. These results were confirmed in ERG-rearranged hormone-naive prostate cancer (HNPC) and CRPC tissue samples. Functional studies demonstrated that ERG has an inhibitory effect on TFF3 expression in hormone-naive cancer but not in the castration-resistant state. In addition, we provide evidence suggesting an effect of androgen receptor signaling on ERG-regulated TFF3 expression. Furthermore, TFF3 overexpression enhances ERG-mediated cell invasion in CRPC prostate cancer cells. Taken together, our findings reveal a novel mechanism for enhanced tumor cell aggressiveness resulting from ERG rearrangement in the castration-resistant setting through TFF3 gene expression.

Indexed as

Chromatin ImmunoprecipitationDisease ProgressionGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMaleNeoplasm InvasivenessNeoplasms, Hormone-DependentPeptidesPolymerase Chain ReactionProstatic NeoplasmsReceptors, AndrogenSequence Analysis, DNASignal TransductionTrans-ActivatorsTranscriptional Regulator ERGERG protein, humanPeptidesReceptors, AndrogenTFF3 protein, humanTrans-ActivatorsTranscriptional Regulator ERGTranscription FactorsTrefoil Factor-3

Identifiers

PMID21170267
PMCPMC3003138
OpenAlexW1850931324

What OpenQuestion holds

Textmetadata
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.