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pmid:37398511
Identification of MiR-223 Associated with Diagnosis in Ectopic Pregnancy.
Jiahan Qiu · Jiaxun Chen · Gaopi Deng · Shuo Yuan
International journal of general medicine · 2023 doi:10.2147/IJGM.S412439
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Experiment
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Complete file
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The hub genes corresponding to the differential miRNA were then identified by using the Xiantao academic tool, GO (Gene Ontology), and KEGG (Kyoto Encyclopedia of Genes and Genomes). Afterward, we used the miEAA database to perform gene set enrichment analysis (GSEA) of differential miRNA, and used Xiantao academic tools again to conduct the ceRNA network based on the target genes. Protein-protein interaction (PPI) network construction and lncRNA of hub miRNA target genes were then predicted by the starbase database. For validation, the villus tissue from intrauterine pregnancy and tubal pregnancy was collected and assayed by qPCR.\nResults: In total 19 differentially expressed miRNAs were screened out, of which MiR-223 had a relatively clear diagnostic significance. Hub genes were enriched and analyzed by GO, KEGG, and GSEA, and the results showed that regulation of NF-κB and other signaling pathways are primarily enriched in ectopic pregnancy. We also obtained 215 key genes from PPI analysis. Our ceRNA analysis indicated that LRRC75A-AS1 and PITPNA-AS1 were associated with MiR-223, and the expression of MiR-223 in qPCR was significantly high in tubal pregnancy group.\nConclusion: We found that MiR-223 can be used in the diagnosis of EP. Our findings provide valuable information and direction for future research into novel targets for EP diagnosis.", "claims": [{"id": "claim-method", "statement": "In this study, we carried out differentially expressed analysis of our dataset using GEO2R for dataset GSE44731 with default values for the options parameters. This time we use the GEOquery8 and limma9 R packages in the Bioconductor project8–10 to acquire comparisons of those processed data tables provided by the original author. In addition, we evaluated the diagnostic efficacy of DEmiRNAs. To do this we drew the ROC curve again using the Xiantao academic tool and calculated the area below the ROC curve (AUC).", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:37398511", "locator": "sections[4] \"Identification of Differentially Expressed miRNAs\" paragraph 3", "quote": "In this study, we carried out differentially expressed analysis of our dataset using GEO2R for dataset GSE44731 with default values for the options parameters."}, {"asset": "source:pmid:37398511", "locator": "sections[4] \"Identification of Differentially Expressed miRNAs\" paragraph 2", "quote": "This time we use the GEOquery8 and limma9 R packages in the Bioconductor project8–10 to acquire comparisons of those processed data tables provided by the original author."}, {"asset": "source:pmid:37398511", "locator": "sections[4] \"Identification of Differentially Expressed miRNAs\" paragraph 3", "quote": "In addition, we evaluated the diagnostic efficacy of DEmiRNAs."}, {"asset": "source:pmid:37398511", "locator": "sections[4] \"Identification of Differentially Expressed miRNAs\" paragraph 3", "quote": "To do this we drew the ROC curve again using the Xiantao academic tool and calculated the area below the ROC curve (AUC)."}], "state": "complete"}, {"id": "claim-data-access", "statement": "The data sets presented in this study can be found in online repositories. 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