Evidence map›Paper›PMID 21575865›Full record

ArticleCancer cell2011

Mechanistic rationale for inhibition of poly(ADP-ribose) polymerase in ETS gene fusion-positive prostate cancer.

J Chad Brenner, Bushra Ateeq, Yong Li, Anastasia K Yocum, Qi Cao, Irfan A Asangani, Sonam Patel, Xiaoju Wang, Hallie Liang, Jindan Yu and 18 more

Erratum issuedOpen access · bronzeAbstract readComment
In one paragraph

Article in Cancer cell, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 248 papers.

0numbers the graph read from it
0cells of the map it votes in
248citing papers in PubMed
23.0field-weighted citation impact, top 1% 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

248 citing papers in PubMed, 420 citations in OpenAlex.

  1. Trial
  2. Targeting Androgen Receptor and DNA Repair in Metastatic Castration-Resistant Prostate Cancer: Results From NCI 9012.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2018
    Trial
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  4. Article
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  7. Article
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  11. Article
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  13. Exploring therapeutic applications ofFrontiers in oncology · 2025
    Review
  14. Review
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  16. Review
  17. Article
  18. Article
  19. Review
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188 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors at 4 institutions in 1 country.

J Chad BrennerMichigan Center for Translational Pathology, University of Michigan, 1400 E. Medical Center Drive, 5316 CCGC, Ann Arbor, MI 48109, USA.
Bushra Ateeq
Yong Li
Anastasia K Yocum
Qi Cao
Irfan A Asangani
Sonam Patel
Xiaoju Wang
Hallie Liang
Jindan Yu
Nallasivam Palanisamy
Javed Siddiqui
Wei Yan
Xuhong Cao
Rohit Mehra
Aaron Sabolch
Venkatesha Basrur
Robert J Lonigro
Jun Yang
Scott A Tomlins
Christopher A Maher
Kojo S J Elenitoba-Johnson
Maha Hussain
Nora M Navone
Kenneth J Pienta
Sooryanarayana Varambally
Felix Y Feng
Arul M Chinnaiyan
University of Michigan–Ann Arbor · USMichigan Center for Translational Pathology · USThe University of Texas MD Anderson Cancer Center · USHoward Hughes Medical Institute · US

Funding

VACCINIA PSA FOR ANDROGEN-MODULATED POST-SURGICAL RECURRENCE OF PROSTATE CANCERP50CA069568 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COONEY, KATHLEEN A · 1995 to 2013
$31.3M
Prostate Cancer Biomarker and Imaging Validation Alliance: Emory University, University of Alabama Birmingham, and University of Texas SouthwesternU01CA113913 · NCI · EMORY UNIVERSITY · PI Martin G. Sanda · 2005 to 2026
$16.4M
Epitomic Biomarkers of Prostate CancerU01CA111275 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHINNAIYAN, ARUL M, RUBIN, MARK A. · 2004 to 2015
$6.8M
Molecuar Sub-typing of Prostate Cancer Based on Recurrent Gene FusionsR01CA132874 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHINNAIYAN, ARUL M · 2009 to 2013
$1.2M
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 P50 CA069568NCI NIH HHS P50CA69568NCI NIH HHS R00 CA129565NCI NIH HHS R01 CA132874NCI NIH HHS R01CA132874NCI NIH HHS U01 CA111275NCI NIH HHS U01 CA113913NCI NIH HHS UO1 CA113913
6 · The paper itself

Abstract

Recurrent fusions of ETS genes are considered driving mutations in a diverse array of cancers, including Ewing's sarcoma, acute myeloid leukemia, and prostate cancer. We investigate the mechanisms by which ETS fusions mediate their effects, and find that the product of the predominant ETS gene fusion, TMPRSS2:ERG, interacts in a DNA-independent manner with the enzyme poly (ADP-ribose) polymerase 1 (PARP1) and the catalytic subunit of DNA protein kinase (DNA-PKcs). ETS gene-mediated transcription and cell invasion require PARP1 and DNA-PKcs expression and activity. Importantly, pharmacological inhibition of PARP1 inhibits ETS-positive, but not ETS-negative, prostate cancer xenograft growth. Finally, overexpression of the TMPRSS2:ERG fusion induces DNA damage, which is potentiated by PARP1 inhibition in a manner similar to that of BRCA1/2 deficiency.

Indexed as

Gene FusionPoly(ADP-ribose) Polymerase InhibitorsAnimalsAntineoplastic AgentsCatalytic DomainCell Line, TumorCell MovementChick EmbryoChromatin ImmunoprecipitationDNA-Activated Protein KinaseDNA DamageEnzyme InhibitorsGene Expression Regulation, NeoplasticGenes, ReporterHEK293 CellsHumansAntineoplastic AgentsDNA-Activated Protein KinaseEnzyme InhibitorsolaparibOncogene Proteins, FusionPARP1 protein, humanPhthalazinesPiperazinesPoly (ADP-Ribose) Polymerase-1Poly(ADP-ribose) Polymerase InhibitorsPoly(ADP-ribose) PolymerasesRecombinant Fusion ProteinsTMPRSS2-ERG fusion protein, human

Identifiers

PMID21575865
PMCPMC3113473
OpenAlexW2151499633

What OpenQuestion holds

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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.