Evidence map›Paper›PMID 19095649›Full record

ArticleThe Journal of biological chemistry2009

Sonic hedgehog-responsive genes in the fetal prostate.

Min Yu, Jerry Gipp, Joon Won Yoon, Phillip Iannaccone, David Walterhouse, Wade Bushman

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

37 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Potential roles of FGF5 as a candidate therapeutic target in prostate cancer.American journal of clinical and experimental urology · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Primary Cilia and Mammalian Hedgehog Signaling.Cold Spring Harbor perspectives in biology · 2017
    Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  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

6 authors at 2 institutions in 1 country.

Min YuUniversity of Wisconsin Medical School, Molecular and Environmental Toxicology Center, Madison, Wisconsin 53705, USA.
Jerry Gipp
Joon Won Yoon
Phillip Iannaccone
David Walterhouse
Wade Bushman
Northwestern University · USUniversity of Wisconsin–Madison · US

Funding

The Role of JunD in Androgen-Induced Changes in Prostate Gland Redox StateP50DK065303 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI BUSHMAN, WADE A. · 2003 to 2007
$4.0M
THE SHH-GLI PATHWAY REGULATES PROSTATE GROWTHR01DK056238 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI BUSHMAN, WADE A · 1999 to 2010
$2.0M
NIDDK NIH HHS P50 DK065303NIDDK NIH HHS R01 DK056238
6 · The paper itself

Abstract

The Hedgehog (Hh) signaling pathway plays an important role in prostate development and appears to play an equally important role in promoting growth of advanced prostate cancer. During prostate development, epithelial cells in the urogenital sinus (UGS) express Sonic Hedgehog (Shh) and secrete Shh peptide. The secreted Hh peptide acts on adjacent mesenchymal cells to activate the Hh signal transduction pathway and elicit paracrine effects on epithelial proliferation and differentiation. To identify mesenchymal targets of Shh signaling, we performed microarray analysis on a Shh-responsive, immortalized urogential sinus mesenchymal cell line. We found 68 genes that were up-regulated by Shh and 21 genes that were down-regulated. Eighteen of those were selected for further study with Ptc1 and Gli1 serving as reference controls. We found 10 of 18 were also Hh-regulated in primary UGS mesenchymal cells and 13 of 18 in the cultured UGS. Seven of 18 exhibited Shh-regulated expression in both assays (Igfbp-6, Igfbp-3, Fbn2, Ntrk3, Agpt4, Dmp1, and Mmp13). Three of the 18 genes contained putative Gli binding motifs that bound Gli1 peptide in electrophoretic mobility shift assays. With the exception of Tiam1, target gene expression generally showed no differences in the concentration dependence of ligand-induced expression, but we observed strikingly different responses to direct pathway activation by transfection with activated Smo, Gli1, and Gli2.

Indexed as

Signal TransductionAnimalsAnimals, NewbornColforsinElectrophoretic Mobility Shift AssayFetusFluorescent Antibody TechniqueGene Expression ProfilingGene Expression Regulation, DevelopmentalHedgehog ProteinsIn Situ HybridizationKruppel-Like Transcription FactorsMaleMesodermMiceOligonucleotide Array Sequence AnalysisColforsinGli1 protein, mouseGli2 protein, mouseHedgehog ProteinsKruppel-Like Transcription FactorsReceptors, G-Protein-CoupledRNA, MessengerSmoothened ReceptorSmo protein, mouseZinc Finger Protein GLI1Zinc Finger Protein Gli2

Identifiers

PMID19095649
PMCPMC2645820
OpenAlexW1963754847

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.