Evidence map›Paper›PMID 35226175›Full record

ArticlePediatric surgery international2022

Yes-associated protein is dysregulated during nitrofen-induced hypoplastic lung development due to congenital diaphragmatic hernia.

Shana Kahnamoui, Naghmeh Khoshgoo, Daywin Patel, Richard Wagner, Richard Keijzer

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Article in Pediatric surgery international, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Mechanical compression causes lung hypoplasia in congenital diaphragmatic hernia with GATA4 genetic variants.American journal of physiology. Lung cellular and molecular physiology · 2026
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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 2 countries.

Shana KahnamouiBiology of Breathing Group, The Children's Hospital Research Institute of Manitoba, Winnipeg, MB, Canada.
Naghmeh KhoshgooBiology of Breathing Group, The Children's Hospital Research Institute of Manitoba, Winnipeg, MB, Canada.
Daywin PatelBiology of Breathing Group, The Children's Hospital Research Institute of Manitoba, Winnipeg, MB, Canada.
Richard WagnerBiology of Breathing Group, The Children's Hospital Research Institute of Manitoba, Winnipeg, MB, Canada.
Richard KeijzerBiology of Breathing Group, The Children's Hospital Research Institute of Manitoba, Winnipeg, MB, Canada. richardkeijzer@gmail.com.
University of Manitoba · CAChildren's Hospital Research Institute of Manitoba · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCongenital diaphragmatic hernia (CDH) is a birth defect associated with abnormal lung development. Yes-associated protein (YAP) is a core kinase of the Hippo pathway, which controls organ size during development. The absence of YAP protein during lung development results in hypoplastic lungs comparable to the lung phenotype in CDH (Mahoney, Dev Cell 30(2):137-150, 2014). We aimed to describe the expression of YAP during normal and nitrofen-induced abnormal lung development.

methodsIntra-gastric administration of dams with 100 mg of nitrofen was used to induce CDH and abnormal lung development in the embryos. Immunofluorescence was performed to visualize the localization of YAP and p-YAP during lung development (E15, E18, E21). Western Blotting was used to determine the abundance of YAP and p-YAP in E21 control and nitrofen-induced hypoplastic CDH lungs.

resultsImmunofluorescence demonstrated cytoplasmic localization of YAP protein in airway epithelial and mesenchymal cells of nitrofen-induced hypoplastic lungs compared to nuclear localization in control lungs. Western Blotting showed a decrease (p = 0.0188) in abundance of YAP (active form) and increase in p-YAP (inactive form) in hypoplastic lungs compared to control lungs.

conclusionOur results demonstrate that YAP protein is mostly phosphorylated, inactive, and expressed in the cytoplasm at the later stages of nitrofen-induced hypoplastic lung development indicating that the alteration in regulation of YAP can be associated with the pathogenesis of abnormal lung development in experimental CDH.

Indexed as

Hernias, Diaphragmatic, CongenitalAnimalsDisease Models, AnimalGene Expression Regulation, DevelopmentalHumansLungPhenyl EthersRatsRats, Sprague-DawleyYAP-Signaling ProteinsnitrofenPhenyl EthersYAP-Signaling ProteinsCongenital diaphragmatic herniaHippo signaling pathwayNitrofen rat modelNormal lung developmentPulmonary hypoplasiaYes-associated protein

Identifiers

PMID35226175
OpenAlexW4214524061

What OpenQuestion holds

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Registered trials

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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.