Evidence map›Paper›PMID 18601749›Full record

ArticleBMC developmental biology2008

CFTR and Wnt/beta-catenin signaling in lung development.

J Craig Cohen, Janet E Larson, Erin Killeen, Damon Love, Ken-Ichi Takemaru

Open access · hybridAbstract read
In one paragraph

Article in BMC developmental biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

23 citing papers in PubMed, 36 citations in OpenAlex.

  1. Disrupting the TGF-β-Wnt Balance to Control the Polarity of the Cystic Fibrosis Airway Epithelium.American journal of respiratory cell and molecular biology · 2024
    Article
  2. Review
  3. ACS pharmacology & translational science · 2023
    Review
  4. Pathological remodeling of distal lung matrix in end-stage cystic fibrosis patients.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2022
    Article
  5. Review
  6. Article
  7. Review
  8. It's about time: clocks in the developing lung.The Journal of clinical investigation · 2020
    Review
  9. Lack of cystic fibrosis transmembrane conductance regulator disrupts fetal airway development in pigs.Laboratory investigation; a journal of technical methods and pathology · 2018
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Colonoscopic screening shows increased early incidence and progression of adenomas in cystic fibrosis.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2016
    Article
  16. Article
  17. Article
  18. Article
  19. Lung organogenesis.Current topics in developmental biology · 2010
    Review
  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

5 authors at 2 institutions in 1 country.

J Craig CohenThe Brady Laboratory, Section of Neonatology, Department of Pediatrics, Stony Brook University, School of Medicine, Stony Brook, New York, USA. jcraig.cohen@stonybrook.edu
Janet E Larson
Erin Killeen
Damon Love
Ken-Ichi Takemaru
Stony Brook School · USStony Brook University · US

Funding

Role of Beta-Catenin Antagonist Chibby in AdipogenesisR01DK073191 · NIDDK · STATE UNIVERSITY NEW YORK STONY BROOK · PI TAKEMARU, KEN-ICHI · 2006 to 2010
$1.5M
NIDDK NIH HHS R01 DK073191
6 · The paper itself

Abstract

backgroundCystic fibrosis transmembrane conductance regulator (CFTR) was shown previously to modify stretch induced differentiation in the lung. The mechanism for CFTR modulation of lung development was examined by in utero gene transfer of either a sense or antisense construct to alter CFTR expression levels. The BAT-gal transgenic reporter mouse line, expressing beta-galactosidase under a canonical Wnt/beta-catenin-responsive promoter, was used to assess the relative roles of CFTR, Wnt, and parathyroid hormone-related peptide (PTHrP) in lung organogenesis. Adenoviruses containing full-length CFTR, a short anti-sense CFTR gene fragment, or a reporter gene as control were used in an intra-amniotic gene therapy procedure to transiently modify CFTR expression in the fetal lung.

resultsA direct correlation between CFTR expression levels and PTHrP levels was found. An inverse correlation between CFTR and Wnt signaling activities was demonstrated.

conclusionThese data are consistent with CFTR participating in the mechanicosensory process essential to regulate Wnt/beta-Catenin signaling required for lung organogenesis.

Indexed as

Signal TransductionAnimalsbeta CateninCystic Fibrosis Transmembrane Conductance RegulatorEmbryo, MammalianGene Expression RegulationLungMiceOrganogenesisParathyroid Hormone-Related ProteinTransfectionWnt Proteinsbeta CateninCystic Fibrosis Transmembrane Conductance RegulatorParathyroid Hormone-Related ProteinWnt Proteins

Identifiers

PMID18601749
PMCPMC2464600
OpenAlexW2122301601

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.