Evidence map›Paper›PMID 32047813›Full record

ArticleBioMed research international2020

Identification of Key Modules, Hub Genes, and Noncoding RNAs in Chronic Rhinosinusitis with Nasal Polyps by Weighted Gene Coexpression Network Analysis.

Xuanchen Zhou, Xiaoyue Zhen, Yiqing Liu, Zhaoyang Cui, Zhiyong Yue, Anting Xu, Jie Han

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 16 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

7 authors at 2 institutions in 1 country.

Xuanchen ZhouDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, China.ORCID https://orcid.org/0000-0002-2098-7266
Xiaoyue ZhenMinimally Invasive Urology Center, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, China.
Yiqing LiuDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, China.
Zhaoyang CuiDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, China.
Zhiyong YueDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, China.
Anting XuDepartment of Otorhinolaryngology and Head and Neck Surgery, The Second Hospital of Shandong University, Jinan 250033, China.ORCID https://orcid.org/0000-0003-3210-5731
Jie HanDepartment of Otorhinolaryngology Head and Neck Surgery, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, China.ORCID https://orcid.org/0000-0003-4868-984X
Shandong University · CNSecond Hospital of Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic rhinosinusitis with nasal polyps (CRSwNP) is a chronic inflammatory disease with relatively easy recurrence. However, the precise molecular mechanisms of this disease are poorly known. Based on gene sequencing data obtained from the Gene Expression Omnibus (GEO) database, we constructed coexpression networks by weighted gene coexpression network analysis (WGCNA). Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses were performed by the Database for Annotation, Visualization, and Integrated Discovery (DAVID). The core gene of pathogenesis, CRSwNP, was screened by protein-protein interaction data (PPI) from the HPRD database. Unsupervised clustering was applied to screen hub genes related to the phenotype of CRSwNP. Blue and turquoise modules were found to be most significantly related to the pathogenicity of CRSwNP. Functional enrichment analysis showed that cell proliferation in the blue modules, the apoptotic process in the turquoise module, and the cancer pathway in both modules were mostly significantly correlated with the development of CRSwNP. The noncoding RNAs (long noncoding RNA and microRNA) and the top 10 core genes in each module were found to be associated with the pathogenesis of CRSwNP. A total of nine hub genes were identified to be related to the CRSwNP phenotype. By qRT-PCR analysis,

Indexed as

TranscriptomeAntigens, CDAntigens, NeoplasmCadherinsClass Ia Phosphatidylinositol 3-KinaseCytokinesDNA-Binding ProteinsGene Expression ProfilingGene OntologyGene Regulatory NetworksHumansLow Density Lipoprotein Receptor-Related Protein-1Membrane Transport ProteinsMucoproteinsNasal PolypsNeoplasm ProteinsAGR2 protein, humanAKT1 protein, humanAntigens, CDAntigens, NeoplasmCadherinsCBL protein, humanCDH1 protein, humanClass Ia Phosphatidylinositol 3-KinaseCytokinesDNA-Binding ProteinsDSE protein, humanFAM3D protein, humanLow Density Lipoprotein Receptor-Related Protein-1LRP1 protein, humanMALAT1 long non-coding RNA, humanMembrane Transport ProteinsMucoproteinsNeoplasm ProteinsOncogene ProteinsPIK3R1 protein, humanPIP protein, humanProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-cblRNA, Long NoncodingRNA, UntranslatedTranscription FactorsXIST non-coding RNA

Identifiers

PMID32047813
PMCPMC7003281
OpenAlexW3001807704

What Socratic 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 Socratic graph.