Evidence map›Paper›PMID 19934349›Full record

ReviewProceedings of the American Thoracic Society2009

Mechanisms of lung development: contribution to adult lung disease and relevance to chronic obstructive pulmonary disease.

Wei Shi, Felicia Chen, Wellington V Cardoso

Open access · greenAbstract readReview
In one paragraph

Review in Proceedings of the American Thoracic Society, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 4% 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

54 citing papers in PubMed, 1 synthesis or guideline pooled it, 99 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. FGF family in health and disease.Molecular biomedicine · 2026
    Review
  4. Article
  5. Article
  6. Dysanapsis Genetic Risk Predicts Lung Function Across the Lifespan.American journal of respiratory and critical care medicine · 2024
    Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Hedgehog Signaling Pathway Orchestrates Human Lung Branching Morphogenesis.International journal of molecular sciences · 2022
    Article
  12. Article
  13. Lung functional development and asthma trajectories.Seminars in immunopathology · 2020
    Review
  14. Article
  15. Effects of Retinoids on Augmentation of Club Cell Secretory Protein.American journal of respiratory and critical care medicine · 2017
    Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Notch signaling in lung diseases: focus on Notch1 and Notch3.Therapeutic advances in respiratory disease · 2016
    Review
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

3 authors at 2 institutions in 1 country.

Wei ShiPulmonary Center, Boston University School of Medicine, 72 East Concord Street, Boston, MA 02118, USA.
Felicia Chen
Wellington V Cardoso
Boston University · USPulmonary Associates · US

Funding

T1alpha in type I cell formation, regulation &functionP01HL047049 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI LU, JINING · 1992 to 2012
$27.6M
RETINOIC ACID SIGNALING IN LUNG MORPHOGENESISR01HL067129 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CARDOSO, WELLINGTON V. · 2001 to 2015
$4.6M
NHLBI NIH HHS 2 R01 HL067129-05NHLBI NIH HHS P01 HL47049
6 · The paper itself

Abstract

Chronic obstructive pulmonary disease (COPD) results in major remodeling of the distal airspaces and changes in the differentiation profile of the airway epithelium. The cellular and molecular mechanisms involved in initiation and progression of this disease are little understood. Although environmental factors, including cigarette smoke, have been directly implicated in the pathogenesis of COPD, genetic risk factors also appear to play a fundamental role in the individual's susceptibility to this disease. Lung development depends on precise coordination of signals, such as fibroblast growth factors (Fgf), Sonic Hedgehog (Shh), retinoic acid, Notch, and Tgf beta. Dramatic changes in the pattern of branching and differentiation of the lung epithelium results from disruption of these signals in genetically altered mice. Recent studies, including whole-genome expression and genome-wide association analyses, suggest that some molecular regulators originally described in developmental processes may be altered in patients with COPD. Whether disturbances in the molecular and cellular events mediated by these genes during development participate in the initiation or exacerbation of COPD, needs further investigation. The role of selected pathways, including Sonic hedgehog, Notch, retinoid, and Tgf beta in the developing lung and the potential association with COPD are discussed.

Indexed as

AnimalsCell DifferentiationHumansLungPulmonary Disease, Chronic ObstructiveSignal Transduction

Identifiers

PMID19934349
PMCPMC3266050
OpenAlexW2044016511

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.