Diagnostic gene biomarkers for predicting immune infiltration in endometriosis.

Objective: To determine the potential diagnostic markers and extent of immune cell infiltration in endometriosis (EMS).Methods: Two published profiles (GSE7305 and GSE25628 datasets) were downloaded, and the candidate biomarkers were identified by support vector machine recursive feature elimination...

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Publicado en:BMC Women's Health Vol. 22; no. 1; pp. 1 - 15
Autores principales: Xie, Chengmao, Lu, Chang, Liu, Yong, Liu, Zhaohui
Formato: Journal Article
Publicado: BioMed Central 5/18/2022
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 5/18/2022
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      pub: BioMed Central
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        NLM35585523
        10.1186/s12905-022-01765-3
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        atl: Diagnostic gene biomarkers for predicting immune infiltration in endometriosis.
      aug:
        au:
          Xie, Chengmao
          Lu, Chang
          Liu, Yong
          Liu, Zhaohui
        affil: Department of Gynecology, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing Maternal and Child Health Care Hospital, 100026, Beijing, China
      sug:
        subj:
          Endometriosis
          Endometriosis Diagnosis
          Female
          Endometrium Metabolism
          Female
      ab: Objective: To determine the potential diagnostic markers and extent of immune cell infiltration in endometriosis (EMS).Methods: Two published profiles (GSE7305 and GSE25628 datasets) were downloaded, and the candidate biomarkers were identified by support vector machine recursive feature elimination analysis and a Lasso regression model. The diagnostic value and expression levels of biomarkers in EMS were verified by quantitative reverse transcription polymerase chain reaction (qRT-PCR) and western blotting, then further validated in the GSE5108 dataset. CIBERSORT was used to estimate the composition pattern of immune cell components in EMS.Results: One hundred and fifty-three differential expression genes (DEGs) were identified between EMS and endometrial with 83 upregulated and 51 downregulated genes. Gene sets related to arachidonic acid metabolism, cytokine-cytokine receptor interactions, complement and coagulation cascades, chemokine signaling pathways, and systemic lupus erythematosus were differentially activated in EMS compared with endometrial samples. Aquaporin 1 (AQP1) and ZW10 binding protein (ZWINT) were identified as diagnostic markers of EMS, which were verified using qRT-PCR and western blotting and validated in the GSE5108 dataset. Immune cell infiltrate analysis showed that AQP1 and ZWINT were correlated with M2 macrophages, NK cells, activated dendritic cells, T follicular helper cells, regulatory T cells, memory B cells, activated mast cells, and plasma cells.Conclusion: AQP1 and ZWINT could be regarded as diagnostic markers of EMS and may provide a new direction for the study of EMS pathogenesis in the future.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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