Evidence map›Paper›PMID 21826097›Full record

ArticleProstate cancer and prostatic diseases2011

Transcriptional and post-transcriptional regulation of Sprouty1, a receptor tyrosine kinase inhibitor in prostate cancer.

M Darimipourain, S Wang, M Ittmann, B Kwabi-Addo

Abstract read
PubMed Publisher
In one paragraph

Article in Prostate cancer and prostatic diseases, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. MiR-21: an environmental driver of malignant melanoma?Journal of translational medicine · 2015
    Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Sprouty genes function in suppression of prostate tumorigenesis.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  11. 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

4 authors at 2 institutions in 1 country.

M DarimipourainHoward University Cancer Center, Washington, DC 20060, USA.
S Wang
M Ittmann
B Kwabi-Addo
Howard University · USBaylor College of Medicine · US

Funding

STEROID RECEPTORS SUPERFAMILY MEMBERS--THEIR ROLE IN PROSTATE CANCERP50CA058204 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ITTMANN, MICHAEL M. · 1992 to 2007
$21.3M
Baylor College of Medicine Cancer CenterP20CA103698 · NCI · BAYLOR COLLEGE OF MEDICINE · PI OSBORNE, C KENT · 2003 to 2005
$1.2M
NCI NIH HHS P20 CA103698NCI NIH HHS P50CA058204
6 · The paper itself

Abstract

Sprouty1 (Spry1) is a negative regulator of fibroblast growth factor signaling with a potential tumor suppressor function in prostate cancer (PCa). Spry1 is downregulated in human PCa, and Spry1 expression can markedly inhibit PCa proliferation in vitro. We have reported DNA methylation as a mechanism for controlling Spry1 expression. However, promoter methylation does not seem to explain gene silencing in all PCa cases studied to suggest other mechanisms of gene inactivation, such as alterations in trans-acting factors and/or post-transcriptional activity may be responsible for the decreased expression in those cases. Binding sites for Wilm's tumor (WT1) transcription factors EGR1, EGR3 and WTE are highly conserved between the mouse and human Spry1 promoter regions, suggesting an evolutionary conserved mechanism(s) involving WT1 and EGR in Spry1 regulation. Spry1 mRNA contains multiple microRNA (miRNA) binding sites in its 3'UTR region suggesting post-transcriptional control. We demonstrate that Spry1 is a target for miR-21-mediated gene silencing. miRNA-based therapeutic approaches to treat cancer are emerging. Spry1 is highly regulated by miRNAs and could potentially be an excellent candidate for such approaches.

Indexed as

Gene Expression Regulation, NeoplasticGene SilencingTranscription, GeneticBase SequenceBinding SitesCell Line, TumorDNA-Binding ProteinsHumansMaleMembrane ProteinsMicroRNAsMolecular Sequence DataPhosphoproteinsPromoter Regions, GeneticProstatic NeoplasmsRNA, MessengerDNA-Binding ProteinsMembrane ProteinsMicroRNAsMIRN21 microRNA, humanPhosphoproteinsRNA, MessengerSPRY1 protein, humanTranscription Factors

Identifiers

PMID21826097
OpenAlexW2058176500

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.