Evidence map›Paper›PMID 26310325›Full record

ArticleBMC cancer2015

The transcription factor ERG increases expression of neurotransmitter receptors on prostate cancer cells.

Haydn T Kissick, Seung T On, Laura K Dunn, Martin G Sanda, John M Asara, Kathryn L Pellegrini, Jonathan K Noel, Mohamed S Arredouani

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Exploring therapeutic applications ofFrontiers in oncology · 2025
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. 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

8 authors at 3 institutions in 1 country.

Haydn T KissickDepartment of Urology, Emory University School of Medicine, Atlanta, GA, USA. haydn.kissick@emory.edu.
Seung T OnDepartment of Surgery, Urology Division, Beth Israel Deaconess Medical Center, Harvard Medical School, 3 Blackfan Circle, E/CLS-446, Boston, MA, 02215, USA. seungtae.on@my.mcphs.edu.
Laura K DunnDepartment of Surgery, Urology Division, Beth Israel Deaconess Medical Center, Harvard Medical School, 3 Blackfan Circle, E/CLS-446, Boston, MA, 02215, USA. laurdunn@gmail.com.
Martin G SandaDepartment of Urology, Emory University School of Medicine, Atlanta, GA, USA. martin.sanda@emory.edu.
John M AsaraDepartment of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA. jasara@bidmc.harvard.edu.
Kathryn L PellegriniDepartment of Urology, Emory University School of Medicine, Atlanta, GA, USA. Kathryn.pellegrini@emory.edu.
Jonathan K NoelDepartment of Surgery, Urology Division, Beth Israel Deaconess Medical Center, Harvard Medical School, 3 Blackfan Circle, E/CLS-446, Boston, MA, 02215, USA. jknoel@hotmail.com.
Mohamed S ArredouaniDepartment of Surgery, Urology Division, Beth Israel Deaconess Medical Center, Harvard Medical School, 3 Blackfan Circle, E/CLS-446, Boston, MA, 02215, USA. simo.arredouani@agenusbio.com.
Harvard University · USEmory University · USBeth Israel Deaconess Medical Center · US

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI A. Heather Eliassen · 1985 to 2026
$330.6M
Tumor and Circulating Markers as Links Between Obesity and Lethal Prostate CanceP50CA090381 · NCI · DANA-FARBER CANCER INSTITUTE · PI LODA, MASSIMO · 2002 to 2017
$36.2M
Tuberous Sclerosis-Pathway and PathogenesisP01CA120964 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI David J. Kwiatkowski · 2007 to 2026
$35.9M
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
NCI NIH HHS 2P50CA90381-06NCI NIH HHS 5P01CA120964NCI NIH HHS 5P30CA006516NCI NIH HHS P01 CA120964NCI NIH HHS P30 CA006516NCI NIH HHS P50 CA090381NCI NIH HHS U01 CA113913NCI NIH HHS UO1-CA113913
6 · The paper itself

Abstract

backgroundThe TMPRSS2-ERG gene fusion occurs in about half of prostate cancer (PCa) cases and results in overexpression of the transcription factor ERG. Overexpression of ERG has many effects on cellular function. However, how these changes enhance cell growth and promote tumor development is unclear.

methodsTo investigate the role of ERG, LNCaP and PC3 cells were transfected with ERG and gene expression and metabolic profile were analyzed.

resultsOur data show that expression of ERG induces overexpression of many nicotinicacetylcholine receptors (nAChRs). In addition, metabolic profiling by LC-MS/MS revealed elevated production of several neurotransmitters in cells expressing ERG. Consistently, treatment of ERG-expressing cells with nicotine induced elevated calcium influx, GSK3β (Ser9) phosphorylation and cell proliferation. Finally, we show that PCa patientswho are smokers have larger tumors if their tumors are TMPRSS2-ERG gene fusion positive.

conclusionCollectively, our data suggest that ERG sensitizes prostate tumor cells to neurotransmitter receptor agonists like nicotine.

Indexed as

CalciumCell Line, TumorCell ProliferationHumansMaleMetabolomeNicotineOncogene Proteins, FusionProstatic NeoplasmsReceptors, NicotinicSmokingTrans-ActivatorsTranscriptional Regulator ERGUp-RegulationCalciumERG protein, humanNicotineOncogene Proteins, FusionReceptors, NicotinicTMPRSS2-ERG fusion protein, humanTrans-ActivatorsTranscriptional Regulator ERG

Identifiers

PMID26310325
PMCPMC4549934
OpenAlexW2168238579

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.