Evidence map›Paper›PMID 40574839›Full record

ArticleFrontiers in immunology2025

Integrated bioinformatics analysis identifies hub genes and immune regulatory networks in HIV infection.

Xiaoxia Pang, Xinghong Chen, Yuxin Jing, Feng Shi, Xiaoying Chen, Huatuo Huang, Chunhong Liu

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Identification and Validation of Hub Genes in Hidradenitis Suppurativa.Clinical, cosmetic and investigational dermatology · 2025
    Article
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.

Xiaoxia Pang *Center for Medical Laboratory Science, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Xinghong Chen *Department of Medical Reproduction Center, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Yuxin Jing *Center for Medical Laboratory Science, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Feng ShiKey Laboratory of Research on Clinical Molecular Diagnosis for High Incidence Diseases in Western Guangxi of Guangxi Higher Education Institutions, Baise, China.
Xiaoying ChenCenter for Medical Laboratory Science, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Huatuo HuangCenter for Medical Laboratory Science, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Chunhong LiuCenter for Medical Laboratory Science, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Acquired Immune Deficiency Syndrome (AIDS) is a chronic and life-threatening condition caused by the human immunodeficiency virus (HIV), which severely weakens the immune system. Despite advances in treatment, AIDS remains incurable. Understanding the molecular mechanisms underlying AIDS progression is crucial for developing effective therapeutic strategies. Therefore, this study aims to identify hub genes associated with AIDS susceptibility and progression, as well as to elucidate potential molecular mechanisms involved. Methods: We used the Gene Expression Omnibus (GEO) dataset GSE76246 for this study. Differentially expressed genes (DEGs) were screened, and Weighted Gene Co-expression Network Analysis (WGCNA) was employed to construct gene modules associated with HIV infection. Hub genes were identified using the CytoHubba plugin, and their expression profiles were assessed using box plots. The diagnostic potential of these genes was evaluated using receiver operating characteristic (ROC) analysis. Functional enrichment and Gene Set Enrichment Analysis (GSEA) were conducted to identify key biological pathways. Additionally, we analyzed immune cell infiltration and constructed drug-gene interaction, miRNA and transcription factor (TF) regulatory networks. Results: 101 intersection genes were identified by combining DEGs, Oxidative stress genes and module genes from WGCNA. Functional enrichment analysis highlighted key pathways, including oxidative stress response and apoptotic signaling. A protein-protein interaction (PPI) network analysis identified 10 hub genes (TP53, AKT1, JUN, CTNNB1, PXDN, MAPK3, FOS, MMP9, FOXO1, STAT1), which showed strong diagnostic potential, as evidenced by ROC curve analysis. Immune infiltration analysis revealed significant associations between hub genes and various immune cell populations. Furthermore, drug-gene interaction analysis predicted several potential therapeutic compounds. Additionally, miRNA and TF regulatory networks were constructed, identifying critical regulatory elements influencing the expression of hub genes. Conclusion: This study identified ten hub genes (TP53, AKT1, JUN, CTNNB1, PXDN, MAPK3, FOS, MMP9, FOXO1, STAT1) that play crucial roles in HIV infection and progression. These genes serve as potential biomarkers for HIV diagnosis and therapeutic targets.

Indexed as

Computational BiologyGene Regulatory NetworksHIV InfectionsDatabases, GeneticGene Expression ProfilingGene Expression RegulationHumansMicroRNAsProtein Interaction MapsTranscriptomeMicroRNAsbioinformatics analysisHIV infectionhub genesimmuneregulatory networks

Identifiers

PMID40574839
PMCPMC12197935

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.