Evidence map›Paper›PMID 37935955›Full record

ArticleScientific reports2023

Exploring the molecular mechanism underlying the psoriasis and T2D by using microarray data analysis.

Li Yang, Lei Zhang, Qingfang Du, Xiaoyu Gong, Jun Tian

Abstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

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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

5 authors.

Li Yang *Department of Dermatology, Shaanxi Provincial People's Hospital, Xi'an, China.
Lei Zhang *Department of Dermatology, Shaanxi Provincial People's Hospital, Xi'an, China.
Qingfang DuDepartment of Dermatology, Shaanxi Provincial People's Hospital, Xi'an, China.
Xiaoyu GongDepartment of Ophthalmology, Shaanxi Provincial People's Hospital, Xi'an, China.
Jun TianDepartment of Dermatology, Shaanxi Provincial People's Hospital, Xi'an, China. sydpg@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although a large number of evidence has identified that psoriasis is significantly correlated with type 2 diabetes (T2D), the common molecular mechanism of its occurrence remains unclear. Our study aims to further elucidate the mechanism of the occurrence of this complication. We obtained the gene expression data of psoriasis (GSE30999) and T2D (GSE28829) from the Gene Expression Omnibus (GEO) dataset. Then the common differentially expressed genes (DEGs) of T2D and psoriasis were identified. After that, we performed three types of analyses about these DEGs, including functional enrichment analysis, protein-protein interaction (PPI) network and module manufacture, hub genes identification and co-expression analysis. 132 common DEGs (14 upregulated genes and 118 downregulated genes) were identified for subsequent a series of analyses. Function enrichment analysis demonstrated that Rap1 signaling pathway, PI3K-Akt signaling pathway, and cGMP-PKG signaling pathway may play a significant role in pathogenesis of psoriasis and T2D. Finally, 3 important hub genes were selected by utilizing cytoHubba, including SNRPN, GNAS, IGF2. Our work reveals the potential common signaling pathways of psoriasis and T2D. These Hub genes and common signaling pathways provide insights for further investigation of molecular mechanism about psoriasis and T2D.

Indexed as

Diabetes Mellitus, Type 2PsoriasisComputational BiologyGene Expression ProfilingGenes, RegulatorHumansPhosphatidylinositol 3-KinasesProtein Interaction MapsPhosphatidylinositol 3-Kinases

Identifiers

PMID37935955
PMCPMC10630520

What Socratic holds

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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 Socratic graph.