Evidence map›Paper›PMID 40300201›Full record

ArticleAnnals of medicine2025

Identification and validation of programmed cell death related biomarkers for the treatment and prevention COVID-19.

Jie Yang, YaoXi Tan, Xing Liu

Abstract readValidation Study
In one paragraph

Article in Annals of medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Jie YangDepartment of Infectious Diseases, Affiliated hospital of Jiangnan University, Wuxi, Jiangsu, China.
YaoXi TanDepartment of Infectious Diseases, Affiliated hospital of Jiangnan University, Wuxi, Jiangsu, China.
Xing LiuDepartment of Emergency, Affiliated Wuxi Fifth Hospital of Jiangnan University, Wuxi, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeProgrammed cell death (PCD) plays a key role in the progression of coronavirus disease 2019 (COVID-19). However, PCD-relevant biomarkers have not been fully discovered. The aim of this study was to explore the PCD-relevant biomarkers for the treatment and prevention of COVID-19.

methodsBioinformatic analyses were performed to explore the clinical relevant PCD genes with differential expression (DE) in COVID-19 compared with matched controls. PPI network was used for hub genes screening and machine learning methods were employed for filtering feature genes. The biomarker genes were screened by Venn diagram. The correlations between biomarkers with clinical features and immune microenvironment were further explored. Biomarker validation was performed in clinical samples by real-time reverse transcriptase-polymerase chain reaction (RT-qPCR).

resultsIn total, 118 clinically relevant and PCD associated differential expressed genes (DEGs) were screened, which were mainly related with apoptosis related pathways, among which six biomarkers (Cyclin B1 (CCNB1), cyclin-dependent kinase 1 (CDK1), interferon regulatory factor 4 (IRF4), lipoteichoic acid (LTA), matrix metallopeptidase 9 (MMP9) and Oncostatin M (OSM)) were identified. The excellent or good diagnostic performance of biomarkers was determined by receiver operating characteristic (ROC) curve analysis. The biomarkers showed diverse correlations with clinical indicators, such as age, sex and Intensive Care Unit (ICU) admission. Total 14 types of immune cells exerted differential infiltration between COVID-19 and controls. Biomarkers were correlated with immune cells at varying levels. COVID-19 was classified in three clusters, which showed differential expression of biomarker genes and significant associations with clinical information, such as sex, age and ICU admission. The DEGs of biomarkers were determined in COVID-19 patients relative to controls.

conclusionThe six biomarkers (CCNB1, CDK1, IRF4, LTA, MMP9 and OSM) can be served as the biomarkers for the treatment and prevention of COVID-19.

Indexed as

ApoptosisCOVID-19AdultAgedBiomarkersComputational BiologyFemaleGene Expression ProfilingHumansInterferon Regulatory FactorsMaleMatrix Metalloproteinase 9Middle AgedSARS-CoV-2BiomarkersInterferon Regulatory FactorsMatrix Metalloproteinase 9clinical featuresCoronavirus disease 2019immune microenvironmentprogrammed cell deathsubtypes classification

Identifiers

PMID40300201
PMCPMC12042234

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