Evidence map›Paper›PMID 22081448›Full record

ArticleThe Journal of pathology2012

β-Catenin determines upper airway progenitor cell fate and preinvasive squamous lung cancer progression by modulating epithelial-mesenchymal transition.

Adam Giangreco, Liwen Lu, Charles Vickers, Vitor Hugo Teixeira, Karen R Groot, Colin R Butler, Ekaterina V Ilieva, P Jeremy George, Andrew G Nicholson, Elizabeth K Sage and 2 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in The Journal of pathology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

39 citing papers in PubMed, 73 citations in OpenAlex.

  1. Article
  2. Review
  3. Cell-cell interactions and communication dynamics in lung fibrosis.Chinese medical journal pulmonary and critical care medicine · 2024
    Review
  4. Article
  5. Human Airway Basal Cells Undergo Reversible Squamous Differentiation and Reshape Innate Immunity.American journal of respiratory cell and molecular biology · 2023
    Article
  6. Basic Science Perspective on Engineering and Modeling the Large Airways.Advances in experimental medicine and biology · 2023
    Article
  7. Review
  8. Article
  9. SARS-CoV-2 Infection and Lung Regeneration.Clinical microbiology reviews · 2022
    Review
  10. Extracellular vesicle-mediated cellular crosstalk in lung repair, remodelling and regeneration.European respiratory review : an official journal of the European Respiratory Society · 2022
    Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. WNT Signalling in Lung Physiology and Pathology.Handbook of experimental pharmacology · 2021
    Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 1 country.

Adam GiangrecoCentre for Respiratory Research, University College London, UK.
Liwen Lu
Charles Vickers
Vitor Hugo Teixeira
Karen R Groot
Colin R Butler
Ekaterina V Ilieva
P Jeremy George
Andrew G Nicholson
Elizabeth K Sage
Fiona M Watt
Sam M Janes
University College London · GBCancer Research UK · GBRoyal Brompton Hospital · GBUniversity College Hospital · GB

Funding

European Research Council 260290Medical Research Council G0800784Medical Research Council G1000355Medical Research Council G1000847Medical Research Council G108/596Wellcome Trust 079249Wellcome Trust 091730
6 · The paper itself

Abstract

Human lung cancers, including squamous cell carcinoma (SCC) are a leading cause of death and, whilst evidence suggests that basal stem cells drive SCC initiation and progression, the mechanisms regulating these processes remain unknown. In this study we show that β-catenin signalling regulates basal progenitor cell fate and subsequent SCC progression. In a cohort of preinvasive SCCs we established that elevated basal cell β-catenin signalling is positively associated with increased disease severity, epithelial proliferation and reduced intercellular adhesiveness. We demonstrate that transgene-mediated β-catenin inhibition within keratin 14-expressing basal cells delayed normal airway repair while basal cell-specific β-catenin activation increased cell proliferation, directed differentiation and promoted elements of early epithelial-mesenchymal transition (EMT), including increased Snail transcription and reduced E-cadherin expression. These observations are recapitulated in normal human bronchial epithelial cells in vitro following both pharmacological β-catenin activation and E-cadherin inhibition, and mirrored our findings in preinvasive SCCs. Overall, the data show that airway basal cell β-catenin determines cell fate and its mis-expression is associated with the development of human lung cancer.

Indexed as

Epithelial-Mesenchymal TransitionAdult Stem CellsAnimalsbeta CateninBiomarkers, TumorCadherinsCarcinoma, Squamous CellCell LineageCell Line, TransformedCell ProliferationCohort StudiesDisease ProgressionFemaleHumansKeratin-14Lung Neoplasmsbeta CateninBiomarkers, TumorCadherinsCTNNB1 protein, humanKeratin-14Krt14 protein, mouseSnail Family Transcription FactorsTranscription Factors

Identifiers

PMID22081448
PMCPMC3434372
OpenAlexW2024166942

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.