Evidence map›Paper›PMID 26944061›Full record

ArticleBMC cardiovascular disorders2016

Weighted gene co-expression network analysis identifies specific modules and hub genes related to coronary artery disease.

Jing Liu, Ling Jing, Xilin Tu

Open access · goldAbstract read
In one paragraph

Article in BMC cardiovascular disorders, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
7.1field-weighted citation impact, top 3% 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

53 citing papers in PubMed, 95 citations in OpenAlex.

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  11. Identification ofFrontiers in molecular biosciences · 2024
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  12. Identification of biomarkers in laryngeal cancer by weighted gene co-expression network analysis.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2023
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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

3 authors at 2 institutions in 1 country.

Jing LiuDepartment of Cardiology, Harbin the second hospital, Harbin, Heilongjiang, 150056, China. JingLiujll@163.com.
Ling JingDepartment of Cardiology, First affiliated hospital of Harbin medical university, Harbin, Heilongjiang, 150036, China. lingjingljj@163.com.
Xilin TuEmergency Internal Medicine, First affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, 150036, China. XilinTuxlt@163.com.
First Affiliated Hospital of Harbin Medical University · CNHarbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe analysis of the potential molecule targets of coronary artery disease (CAD) is critical for understanding the molecular mechanisms of disease. However, studies of global microarray gene co-expression analysis of CAD still remain limited.

methodsMicroarray data of CAD (GSE23561) were downloaded from Gene Expression Omnibus, including peripheral blood samples from CAD patients (n = 6) and controls (n = 9). Limma package in R was used to identify the differentially expressed genes (DEGs) between CAD and control samples. Using weighted gene co-expression network analysis (WGCNA) package in R, WGCNA was performed to identify significant modules in the network. Then, functional and pathway enrichment analyses were conducted for genes in the most significant module using DAVID software. Moreover, hub genes in the module were analyzed by isubpathwayminer package in R and GenCLiP 2.0 tool to identify the significant sub-pathways.

resultsTotal 3711 DEGs and 21 modules for them were identified in CAD samples. The most significant module was associated with the pathways of hypertrophic cardiomyopathy and membrane related functions. In addition, the top 30 hub genes with high connectivity in the module were selected, and two genes (G6PD and S100A7) were taken as key molecules via sub-pathway screening and data mining.

conclusionsA module associated with hypertrophic cardiomyopathy pathway was detected in CAD samples. G6PD and S100A7 were the potential targets in CAD. Our finding might provide novel insight into the underlying molecular mechanism of CAD.

Indexed as

Gene Regulatory NetworksGenetic MarkersCardiomyopathy, HypertrophicCase-Control StudiesComputational BiologyCoronary Artery DiseaseDatabases, GeneticData MiningFemaleGene Expression ProfilingGene Expression RegulationGenetic Association StudiesGenetic Predisposition to DiseaseGlucosephosphate DehydrogenaseHumansMaleGenetic MarkersGlucosephosphate DehydrogenaseRNA, MessengerS100A7 protein, humanS100 Calcium Binding Protein A7S100 Proteins

Identifiers

PMID26944061
PMCPMC4779223
OpenAlexW2292474197

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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.