Evidence map›Paper›PMID 19597533›Full record

ArticleProstate cancer and prostatic diseases2010

Quantitative expression of TMPRSS2 transcript in prostate tumor cells reflects TMPRSS2-ERG fusion status.

K Mwamukonda, Y Chen, L Ravindranath, B Furusato, Y Hu, J Sterbis, D Osborn, I Rosner, I A Sesterhenn, D G McLeod and 2 more

Abstract read
In one paragraph

Article in Prostate cancer and prostatic diseases, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.4field-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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Serine Protease Inhibitors to Treat Lung Inflammatory Diseases.Advances in experimental medicine and biology · 2021
    Review
  5. Article
  6. Article
  7. Article
  8. Biomarkers in prostate cancer: new era and prospective.Medical oncology (Northwood, London, England) · 2014
    Review
  9. Article
  10. Article
  11. Article
  12. Article
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  14. Article
  15. 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

12 authors at 3 institutions in 2 countries.

K MwamukondaUrology Service, Department of Surgery, Walter Reed Army Medical Center, Washington, DC, USA.
Y Chen
L Ravindranath
B Furusato
Y Hu
J Sterbis
D Osborn
I Rosner
I A Sesterhenn
D G McLeod
S Srivastava
G Petrovics
Uniformed Services University of the Health Sciences · USWalter Reed Army Institute of Research · USArmed Forces Institute of Pathology · PK

Funding

Cell Specific Expression Signatures in Prostate CancerR01DK065977 · NIDDK · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI SRIVASTAVA, SHIV · 2004 to 2007
$688k
NIDDK NIH HHS 5R01 DK065977NIDDK NIH HHS R01 DK065977
6 · The paper itself

Abstract

TMPRSS2-ERG fusion is the most common oncogenic rearrangement in prostate cancer (CaP). Owing to this chromosomal rearrangement one TMPRSS2 allele loses its promoter, and one of the ETS-related gene (ERG) alleles gains that promoter leading to its overexpression in these tumor cells. Some studies suggest that TMPRSS2, an androgen-regulated type II transmembrane serine protease, may have an effect on CaP progression. We hypothesized that a difference in TMPRSS2 expression may be present in vivo between CaP cells with and without TMPRSS2-ERG fusion, or a compensatory mechanism for the allelic loss of TMPRSS2 may balance that expression difference. Therefore, TMPRSS2 mRNA expression was evaluated in microdissected CaP cells with and without TMPRSS2-ERG fusion in 132 CaP patients and analyzed for its correlation with other androgen receptor (AR)-regulated genes and clinicopathological features. In vivo TMPRSS2 expression correlated with that of other AR-regulated genes, including PSA/KLK3 and PMEPA1, offering potential as AR surrogates. A significantly reduced expression of TMPRSS2 was evident in malignant cells harboring TMPRSS2-ERG fusion, but not in CaP cells without TMPRSS2-ERG fusion, further defining these two genetically distinct types of CaP.

Indexed as

Gene Expression Regulation, NeoplasticHumansMaleOncogene Proteins, FusionProstateProstatic NeoplasmsRNA, MessengerSerine EndopeptidasesOncogene Proteins, FusionRNA, MessengerSerine EndopeptidasesTMPRSS2-ERG fusion protein, humanTMPRSS2 protein, human

Identifiers

PMID19597533
PMCPMC2820150
OpenAlexW2049198834

What OpenQuestion holds

Textmetadata
LicenceTDM
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.