Evidence map›Paper›PMID 38152085›Full record

ArticleERJ open research2023

Epithelial-mesenchymal transition changes in nonsmall cell lung cancer patients with early COPD.

Wenying Lu, Mathew Suji Eapen, Ashutosh Hardikar, Collin Chia, Iain Robertson, Gurpreet Kaur Singhera, Tillie L Hackett, Sukhwinder Singh Sohal

Open access · goldAbstract read
In one paragraph

Article in ERJ open research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Wenying LuRespiratory Translational Research Group, School of Health Sciences, University of Tasmania, Newnham, TAS, Australia.ORCID https://orcid.org/0000-0003-1550-2276
Mathew Suji EapenRespiratory Translational Research Group, School of Health Sciences, University of Tasmania, Newnham, TAS, Australia.ORCID https://orcid.org/0000-0003-0570-7059
Ashutosh HardikarDepartment of Cardiothoracic Surgery, Royal Hobart Hospital, Hobart, TAS, Australia.ORCID https://orcid.org/0000-0003-3558-6454
Collin ChiaRespiratory Translational Research Group, School of Health Sciences, University of Tasmania, Newnham, TAS, Australia.
Iain RobertsonRespiratory Translational Research Group, School of Health Sciences, University of Tasmania, Newnham, TAS, Australia.
Gurpreet Kaur SingheraDepartment of Anesthesiology, Pharmacology and Therapeutics, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.
Tillie L HackettDepartment of Anesthesiology, Pharmacology and Therapeutics, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.
Sukhwinder Singh SohalRespiratory Translational Research Group, School of Health Sciences, University of Tasmania, Newnham, TAS, Australia.
University of Tasmania · AUUniversity of British Columbia · CARoyal Hobart Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Epithelial-mesenchymal transition (EMT) might be central to lung cancer development in smokers and COPD. We illustrate EMT changes in a broader demographic of patient groups who were diagnosed with nonsmall cell lung cancer (adenocarcinoma and squamous cell carcinoma). These included COPD current and ex-smokers, patients with small airway disease and normal lung function smokers compared to normal controls. Methods: We had access to surgically resected small airway tissue from 46 subjects and assessed for airway wall thickness and immunohistochemically for the EMT biomarkers E-cadherin, N-cadherin, S100A4, vimentin and epidermal growth factor receptor (EGFR). All tissue analysis was done with a computer and microscope-assisted Image-Pro Plus 7.0 software. Results: Airway wall thickness significantly increased across all pathological groups (p<0.05) compared to normal controls. Small airway epithelial E-cadherin expression markedly decreased (p<0.01), and increases in N-cadherin, vimentin, S100A4 and EGFR expression were observed in all pathological groups compared to normal controls (p<0.01). Vimentin-positive cells in the reticular basement membrane, lamina propria and adventitia showed a similar trend to epithelium across all pathological groups (p<0.05); however, such changes were only observed in reticular basement membrane for S100A4 (p<0.05). Vimentin was higher in adenocarcinoma Conclusion: EMT is an active process in the small airway of smokers and COPD diagnosed with nonsmall cell lung cancer, contributing to small airway remodelling and cancer development as seen in these patients.

Identifiers

PMID38152085
PMCPMC10752287
OpenAlexW4388220276

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.