Evidence map›Paper›PMID 38586100›Full record

ArticleAmerican journal of translational research2024

Screening of potential biomarkers in propofol-induced neurotoxicity via bioinformatics prediction and experimental verification.

Tianping He, Jianfeng Huang, Bo Peng, Mianhui Wang, Qiuhao Shui, Liang Cai

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Article in American journal of translational research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Tianping HeDepartment of Anesthesiology, Luxian People's Hospital Luzhou 646100, Sichuan, China.
Jianfeng HuangDepartment of Anesthesiology, Luxian People's Hospital Luzhou 646100, Sichuan, China.
Bo PengDepartment of Anesthesiology, Luxian People's Hospital Luzhou 646100, Sichuan, China.
Mianhui WangDepartment of Anesthesiology, Luxian People's Hospital Luzhou 646100, Sichuan, China.
Qiuhao ShuiDepartment of Anesthesiology, Luxian People's Hospital Luzhou 646100, Sichuan, China.
Liang CaiDepartment of Anesthesiology, The People's Hospital of Leshan Leshan 614013, Sichuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo identify hub genes and biological processes of propofol-induced neurotoxicity and promote the development of pediatric anesthesiology.

methodsWe downloaded the GSE106799 dataset from the Gene Expression Omnibus database. Differentially expressed genes (DEGs) were screened, then Kyoto Encyclopedia of Genes and Genomes, Gene Ontology and Gene Set Enrichment analyses were performed on all DEGs. We identified potential ferroptosis genes in the pathogenesis of propofol-induced neurotoxicity. A key module was obtained after performing weighted gene co-expression network analysis (WGCNA) on the GSE106799 dataset. Hub genes were identified after the least absolute shrinkage and selection operator (LASSO) regression analysis of the intersection of DEGs and genes from the key module. We established a competing endogenous RNA network and predicted potential drugs according to the hub genes. Total RNA and proteins were extracted for real-time quantitative polymerase chain reaction and Western blotting, respectively.

resultsA total of 112 DEGs, including 76 upregulated and 36 downregulated ones were screened out. Propofol-induced neurotoxicity involved processes such as nervous system development, activation of JAK/STAT and MAPK signaling pathways, vascular regeneration, and oxidative stress. The results of WGCNA suggested that the tan module was the most strongly associated with propofol-induced neurotoxicity. We identified 4 hub genes (

conclusionsPrevious studies have demonstrated that

Indexed as

neurotoxicitypotential biomarkersPropofol

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PMID38586100
PMCPMC10994811

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