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pmid:39552710

Identification of hub genes and pathways in Uterine corpus endometrial carcinoma (UCEC): A comprehensive in silico study.

Mahsa Ejlalidiz · Ameneh Mehri-Ghahfarrokhi · Mohammadreza Saberiyan

Biochemistry and biophysics reports · 2024 doi:10.1016/j.bbrep.2024.101860

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:39552710
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science-record
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2026-11-01T20:29:49Z
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paper object · 10 fields
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title
Identification of hub genes and pathways in Uterine corpus endometrial carcinoma (UCEC): A comprehensive in silico study.
doi
10.1016/j.bbrep.2024.101860
pmid
39552710
authors array · 3 items
[0]
Mahsa Ejlalidiz
[1]
Ameneh Mehri-Ghahfarrokhi
[2]
Mohammadreza Saberiyan
journal
Biochemistry and biophysics reports
year
2024
abstract
Background: Uterine corpus endometrial carcinoma (UCEC), derived from the endometrium, is the most common type of endometrial malignasis. This gynecological malignancy is very common all over the world, especially in developed countries and shows a potentially rising trend correlated with the increase in obese women. Methods: Differentially Expressed Genes (DEGs) analysis was conducted on GSE7305 and GSE25628 datasets from the Gene Expression Omnibus (GEO). DEGs were identified using GEO2R (adjusted p-value <0.05, |logFC| > 1). Pathway analysis employed KEGG and Gene Ontology databases, while protein-protein interactions were analyzed using Cytoscape and Gephi. GEPIA was used for target gene validation. Results: We have identified 304 common DEGs and 78 hub genes using GEO and PPI analysis, respectively. The GO and KEGG pathways analysis revealed enrichment of DEGs in extracellular matrix structural constituent, extracellular space, cell adhesion, and ECM-receptor interaction. GEPIA analysis identified three genes, ENG, GNG4, and ECT2, whose expression significantly differed between normal and tumor samples. Conclusion: This analysis study identified the hub genes and associated pathways involved in the pathogenesis of UCEC. The identified hub genes exhibit remarkable potential as diagnostic biomarkers, providing a significant opportunity for early diagnosis and more effective therapeutic approaches for UCEC.
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DEGs were identified using GEO2R (adjusted p-value <0.05, |logFC| > 1).
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DEGs were identified using GEO2R (adjusted p-value <0.05, |logFC| > 1).
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GSE7305: This dataset consists of 20 human tissue samples, evenly divided between diseased endometrial (n = 10) and normal endometrium (n = 10). The dataset employed the Affymetrix Human Genome U133 Plus 2.0 Array (GPL570) microarray platform.
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We have identified 304 common DEGs and 78 hub genes using GEO and PPI analysis, respectively.
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We have identified 304 common DEGs and 78 hub genes using GEO and PPI analysis, respectively.
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We have identified 304 common DEGs and 78 hub genes using GEO and PPI analysis, respectively.
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Human endometriosis vs normal endometrium study - transcriptional profiling
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Complete file
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This gynecological malignancy is very common all over the world, especially in developed countries and shows a potentially rising trend correlated with the increase in obese women.\nMethods: Differentially Expressed Genes (DEGs) analysis was conducted on GSE7305 and GSE25628 datasets from the Gene Expression Omnibus (GEO). DEGs were identified using GEO2R (adjusted p-value <0.05, |logFC| > 1). Pathway analysis employed KEGG and Gene Ontology databases, while protein-protein interactions were analyzed using Cytoscape and Gephi. GEPIA was used for target gene validation.\nResults: We have identified 304 common DEGs and 78 hub genes using GEO and PPI analysis, respectively. The GO and KEGG pathways analysis revealed enrichment of DEGs in extracellular matrix structural constituent, extracellular space, cell adhesion, and ECM-receptor interaction. GEPIA analysis identified three genes, ENG, GNG4, and ECT2, whose expression significantly differed between normal and tumor samples.\nConclusion: This analysis study identified the hub genes and associated pathways involved in the pathogenesis of UCEC. 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