Evidence map›Paper›PMID 22826436›Full record

ArticleMolecular and cellular biology2012

Foxm1 mediates cross talk between Kras/mitogen-activated protein kinase and canonical Wnt pathways during development of respiratory epithelium.

I-Ching Wang, Jonathan Snyder, Yufang Zhang, Julie Lander, Yuto Nakafuku, James Lin, Gang Chen, Tanya V Kalin, Jeffrey A Whitsett, Vladimir V Kalinichenko

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

48 citing papers in PubMed, 65 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. CRISPR-Cas9 Genome Editing Allows Generation of the Mouse Lung in a Rat.American journal of respiratory and critical care medicine · 2024
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  11. Nanoparticle Delivery Systems with Cell-Specific Targeting for Pulmonary Diseases.American journal of respiratory cell and molecular biology · 2021
    Review
  12. American journal of respiratory and critical care medicine · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Postnatal Alveologenesis Depends on FOXF1 Signaling in c-KITAmerican journal of respiratory and critical care medicine · 2019
    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

10 authors at 1 institution in 1 country.

I-Ching WangDivisions of Pulmonary Biology, Perinatal Institute of the Cincinnati Children’s Hospital Research Foundation, Cincinnati, OH, USA. I-Ching.Wang@cchmc.org
Jonathan Snyder
Yufang Zhang
Julie Lander
Yuto Nakafuku
James Lin
Gang Chen
Tanya V Kalin
Jeffrey A Whitsett
Vladimir V Kalinichenko
Cincinnati Children's Hospital Medical Center · US

Funding

Fox Transcription Factors in Development of Pulmonary CapillariesR01HL084151 · NHLBI · UNIVERSITY OF CHICAGO · PI KALINICHENKO, VLADIMIR · 2006 to 2018
$4.9M
Role of Foxm1 in Lung Cancer MicroenvironmentR01CA142724 · NCI · CINCINNATI CHILDRENS HOSP MED CTR · PI KALIN, TANYA · 2010 to 2014
$1.5M
NCI NIH HHS R01 CA142724NHLBI NIH HHS R01 HL084151NHLBI NIH HHS R01 HL84151
6 · The paper itself

Abstract

While Kras/mitogen-activated protein kinase (MAPK) and canonical Wnt/β-catenin are critical for lung morphogenesis, mechanisms integrating these important signaling pathways during lung development are unknown. Herein, we demonstrate that the Foxm1 transcription factor is a key downstream target of activated Kras(G12D). Deletion of Foxm1 from respiratory epithelial cells during lung formation prevented structural abnormalities caused by activated Kras(G12D). Kras/Foxm1 signaling inhibited the activity of canonical Wnt signaling in the developing lung in vivo. Foxm1 decreased T-cell factor (TCF) transcriptional activity induced by activated β-catenin in vitro. Depletion of Foxm1 by short interfering RNA (siRNA) increased nuclear localization of β-catenin, increased expression of β-catenin target genes, and decreased mRNA and protein levels of the β-catenin inhibitor Axin2. Axin2 mRNA was reduced in distal lung epithelium of Foxm1-deficient mice. Foxm1 directly bound to and increased transcriptional activity of the Axin2 promoter region. Foxm1 is required for Kras signaling in distal lung epithelium and provides a mechanism integrating Kras and canonical Wnt/β-catenin signaling during lung development.

Indexed as

Wnt Signaling PathwayAnimalsAxin Proteinbeta CateninForkhead Box Protein M1Forkhead Transcription FactorsGene DeletionGene Expression Regulation, DevelopmentalLungMAP Kinase Signaling SystemMiceMitogen-Activated Protein KinasesProto-Oncogene Proteins p21(ras)Respiratory MucosaTranscriptional ActivationWnt ProteinsAxin2 protein, mouseAxin Proteinbeta CateninForkhead Box Protein M1Forkhead Transcription FactorsFoxm1 protein, mouseHras protein, mouseMitogen-Activated Protein KinasesProto-Oncogene Proteins p21(ras)Wnt Proteins

Identifiers

PMID22826436
PMCPMC3457538
OpenAlexW2020684359

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.