Evidence map›Paper›PMID 29228930›Full record

ArticleBMC pulmonary medicine2017

Gene expression analysis in asthma using a targeted multiplex array.

Christopher D Pascoe, Ma'en Obeidat, Bryna A Arsenault, Yunlong Nie, Stephanie Warner, Dorota Stefanowicz, Samuel J Wadsworth, Jeremy A Hirota, S Jasemine Yang, Delbert R Dorscheid and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMC pulmonary medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 32 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

14 authors at 4 institutions in 1 country.

Christopher D PascoeUBC Institute for Heart Lung Health, St. Paul's Hospital, 1081 Burrard St, Vancouver, BC, Canada. cpascoe@chrim.ca.
Ma'en ObeidatUBC Institute for Heart Lung Health, St. Paul's Hospital, 1081 Burrard St, Vancouver, BC, Canada.
Bryna A ArsenaultUBC Institute for Heart Lung Health, St. Paul's Hospital, 1081 Burrard St, Vancouver, BC, Canada.
Yunlong NieUBC Institute for Heart Lung Health, St. Paul's Hospital, 1081 Burrard St, Vancouver, BC, Canada.
Stephanie WarnerUBC Institute for Heart Lung Health, St. Paul's Hospital, 1081 Burrard St, Vancouver, BC, Canada.
Dorota StefanowiczUBC Institute for Heart Lung Health, St. Paul's Hospital, 1081 Burrard St, Vancouver, BC, Canada.
Samuel J WadsworthUBC Institute for Heart Lung Health, St. Paul's Hospital, 1081 Burrard St, Vancouver, BC, Canada.
Jeremy A HirotaDivision of Respirology, Department of Medicine, McMaster University, Hamilton, ON, Canada.
S Jasemine YangUBC Institute for Heart Lung Health, St. Paul's Hospital, 1081 Burrard St, Vancouver, BC, Canada.
Delbert R DorscheidUBC Institute for Heart Lung Health, St. Paul's Hospital, 1081 Burrard St, Vancouver, BC, Canada.
Chris CarlstenUBC Institute for Heart Lung Health, St. Paul's Hospital, 1081 Burrard St, Vancouver, BC, Canada.
Tillie L HackettUBC Institute for Heart Lung Health, St. Paul's Hospital, 1081 Burrard St, Vancouver, BC, Canada.
Chun Y SeowUBC Institute for Heart Lung Health, St. Paul's Hospital, 1081 Burrard St, Vancouver, BC, Canada.
Peter D ParéUBC Institute for Heart Lung Health, St. Paul's Hospital, 1081 Burrard St, Vancouver, BC, Canada.
St. Paul's Hospital · CASt. Paul's Hospital · CAUniversity of British Columbia · CAMcMaster University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGene expression changes in the structural cells of the airways are thought to play a role in the development of asthma and airway hyperresponsiveness. This includes changes to smooth muscle contractile machinery and epithelial barrier integrity genes. We used a targeted gene expression arrays to identify changes in the expression and co-expression of genes important in asthma pathology.

methodsRNA was isolated from the airways of donor lungs from 12 patients with asthma (8 fatal) and 12 non-asthmatics controls and analyzed using a multiplexed, hypothesis-directed platform to detect differences in gene expression. Genes were grouped according to their role in airway dysfunction: airway smooth muscle contraction, cytoskeleton structure and regulation, epithelial barrier function, innate and adaptive immunity, fibrosis and remodeling, and epigenetics.

resultsDifferential gene expression and gene co-expression analyses were used to identify disease associated changes in the airways of asthmatics. There was significantly decreased abundance of integrin beta 6 and Ras-Related C3 Botulinum Toxin Substrate 1 (RAC1) in the airways of asthmatics, genes which are known to play an important role in barrier function. Significantly elevated levels of Collagen Type 1 Alpha 1 (COL1A1) and COL3A1 which have been shown to modulate cell proliferation and inflammation, were found in asthmatic airways. Additionally, we identified patterns of differentially co-expressed genes related to pathways involved in virus recognition and regulation of interferon production. 7 of 8 pairs of differentially co-expressed genes were found to contain CCCTC-binding factor (CTCF) motifs in their upstream promoters.

conclusionsChanges in the abundance of genes involved in cell-cell and cell-matrix interactions could play an important role in regulating inflammation and remodeling in asthma. Additionally, our results suggest that alterations to the binding site of the transcriptional regulator CTCF could drive changes in gene expression in asthmatic airways. Several asthma susceptibility loci are known to contain CTCF motifs and so understanding the role of this transcription factor may expand our understanding of asthma pathophysiology and therapeutic options.

Indexed as

AsthmaRespiratory HypersensitivityAirway RemodelingCanadaExtracellular MatrixGene Expression ProfilingGene Expression RegulationGenome-Wide Association StudyHumansAsthmaCo-expressionCTCFEpitheliumExtracellular matrixNanostringRemodelingSmooth muscleTargeted expression

Identifiers

PMID29228930
PMCPMC5725935
OpenAlexW2774633803

What OpenQuestion holds

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LicenceCC BY
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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.