Evidence map›Paper›PMID 23308271›Full record

ArticlePloS one2013

Analysis of the Sonic Hedgehog signaling pathway in normal and abnormal bladder development.

Kristin R DeSouza, Monalee Saha, Ashley R Carpenter, Melissa Scott, Kirk M McHugh

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Urothelial generation and regeneration in development, injury, and cancer.Developmental dynamics : an official publication of the American Association of Anatomists · 2017
    Review
  10. Fgfr2 is integral for bladder mesenchyme patterning and function.American journal of physiology. Renal physiology · 2017
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Fgfr2 is integral for bladder mesenchyme patterning and function.American journal of physiology. Renal physiology · 2015
    Article
  16. 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

5 authors at 1 institution in 1 country.

Kristin R DeSouzaCenter for Molecular and Human Genetics, The Research Institute at Nationwide Children's Hospital, Columbus, Ohio, United States of America. kristin.desouza@nationwidechildrens.org
Monalee Saha
Ashley R Carpenter
Melissa Scott
Kirk M McHugh
Nationwide Children's Hospital · US

Funding

Model of Congenital Obstructive Nephropathy-Biomarker & Therapeutic DevelopmentR01DK085242 · NIDDK · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI BATES, CARLTON MATTHEW, MCHUGH, KIRK M. · 2010 to 2014
$1.6M
Characterizing the Molecular Pathways of Bladder Smooth Muscle DevelopmentF32DK089733 · NIDDK · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI DESOUZA, KRISTIN R · 2011 to 2012
$87k
NIDDK NIH HHS F32 DK089733NIDDK NIH HHS R01 DK085242
6 · The paper itself

Abstract

In this study, we examined the expression of Sonic Hedgehog, Patched, Gli1, Gli2, Gli3 and Myocardin in the developing bladders of male and female normal and megabladder (mgb-/-) mutant mice at embryonic days 12 through 16 by in situ hybridization. This analysis indicated that each member of the Sonic Hedgehog signaling pathway as well as Myocardin displayed distinct temporal and spatial patterns of expression during normal bladder development. In contrast, mgb-/- bladders showed both temporal and spatial changes in the expression of Patched, Gli1 and Gli3 as well as a complete lack of Myocardin expression. These changes occurred primarily in the outer mesenchyme of developing mgb-/- bladders consistent with the development of an amuscular bladder phenotype in these animals. These results provide the first comprehensive analysis of the Sonic Hedgehog signaling pathway during normal bladder development and provide strong evidence that this key signaling cascade is critical in establishing radial patterning in the developing bladder. In addition, the lack of detrusor smooth muscle development observed in mgb-/- mice is associated with bladder-specific temporospatial changes in Sonic Hedgehog signaling coupled with a lack of Myocardin expression that appears to result in altered patterning of the outer mesenchyme and poor initiation and differentiation of smooth muscle cells within this region of the developing bladder.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsBody PatterningCell DifferentiationEmbryo, MammalianFemaleHedgehog ProteinsKruppel-Like Transcription FactorsMaleMesodermMiceMice, KnockoutMuscle, SmoothMyocardinNerve Tissue ProteinsNuclear ProteinsGli1 protein, mouseGli2 protein, mouseGli3 protein, mouseHedgehog ProteinsKruppel-Like Transcription FactorsMyocardinNerve Tissue ProteinsNuclear ProteinsPatched ReceptorsReceptors, Cell SurfaceShh protein, mouseTrans-ActivatorsZinc Finger Protein GLI1Zinc Finger Protein Gli2Zinc Finger Protein Gli3

Identifiers

PMID23308271
PMCPMC3538723
OpenAlexW2022357825

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.