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pmid:38274342

Identification of differentially expressed genes associated with ferroptosis in Crohn's disease.

Wenquan Zhang · Zhaoshui Li · Hongbo Li · Dianliang Zhang

Experimental and therapeutic medicine · 2024 doi:10.3892/etm.2024.12378

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complete

Experiment

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Data

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Analysis

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:38274342
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title
Identification of differentially expressed genes associated with ferroptosis in Crohn's disease.
doi
10.3892/etm.2024.12378
pmid
38274342
authors array · 4 items
[0]
Wenquan Zhang
[1]
Zhaoshui Li
[2]
Hongbo Li
[3]
Dianliang Zhang
journal
Experimental and therapeutic medicine
year
2024
abstract
Ferroptosis-related genes may play a critical regulatory role in the pathogenesis of Crohn's disease (CD). The purpose of the present study was to identify genes expressed in CD that are associated with ferroptosis, and to provide guidance in the diagnosis and therapy of CD. CD mRNA expression data were initially gathered from the Gene Expression Omnibus (GEO) database. GSE75214 and GSE102133 datasets were selected as the major targets and were analyzed for differentially expressed genes (DEGs). Subsequently, R software was used to analyze the common genes among the DEGs between CD and ferroptosis-related genes. Gene Ontology enrichment analysis and Kyoto Encyclopedia of Genes and Genome pathway analysis were conducted to identify related pathways and functions. Protein-protein interaction (PPI) analysis was performed to identify target genes. The DSigDB website was used to predict potential target drugs for hub genes. Reverse transcription-quantitative (RT-q) PCR was employed to detect the expression of these ferroptosis-related genes in clinical samples obtained from healthy controls and patients with CD. According to the two GEO datasets, 13 ferroptosis DEGs (11 upregulated genes and two downregulated genes) were identified in CD with thresholds of P<0.05 and |log2 fold change|>1, and were selected for further analysis. PPI analysis indicated the mutual effects among these genes and filtered out five hub genes. The top 10 potential targeted drugs were selected. The qPCR results showed that the expression levels of three genes, namely, IL-6, prostaglandin-endoperoxide synthase 2 (PTGS2) and dual oxidase 2 (DUOX2), were different between CD samples and healthy samples. This result was consistent with the results obtained from the bioinformatics analysis. In conclusion, bioinformatics analysis identified a total of 13 ferroptosis-associated genes in CD. Further verification by qPCR showed that IL-6, PTGS2 and DUOX2 may affect the process of CD by regulating ferroptosis. These findings might provide new biomarkers, diagnostic and therapeutic markers for CD.
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In the qPCR experiment, the results were analyzed by unpaired Student's t-test.
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sections[12] "Statistical analysis" paragraph 2
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In the qPCR experiment, the results were analyzed by unpaired Student's t-test.
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The datasets generated and/or analyzed during the current study are available in the GEO repository, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE102133 and https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE75214. Other datasets used and/or analyzed during the current study are available from the corresponding authors on reasonable request.
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sections[23] "Availability of data and materials" paragraph 2
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The datasets generated and/or analyzed during the current study are available in the GEO repository, https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE102133 and https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE75214. Other datasets used and/or analyzed during the current study are available from the corresponding authors on reasonable request.
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Analysis of the two GEO datasets identified 13 ferroptosis-related differentially expressed genes in Crohn's disease.
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According to the two GEO datasets, 13 ferroptosis DEGs (11 upregulated genes and two downregulated genes) were identified in CD with thresholds of P<0.05 and |log2 fold change|>1, and were selected for further analysis.
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sections[0] "Abstract" paragraph 1
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According to the two GEO datasets, 13 ferroptosis DEGs (11 upregulated genes and two downregulated genes) were identified in CD with thresholds of P<0.05 and |log2 fold change|>1, and were selected for further analysis.
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Complete file
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The purpose of the present study was to identify genes expressed in CD that are associated with ferroptosis, and to provide guidance in the diagnosis and therapy of CD. CD mRNA expression data were initially gathered from the Gene Expression Omnibus (GEO) database. GSE75214 and GSE102133 datasets were selected as the major targets and were analyzed for differentially expressed genes (DEGs). Subsequently, R software was used to analyze the common genes among the DEGs between CD and ferroptosis-related genes. Gene Ontology enrichment analysis and Kyoto Encyclopedia of Genes and Genome pathway analysis were conducted to identify related pathways and functions. Protein-protein interaction (PPI) analysis was performed to identify target genes. The DSigDB website was used to predict potential target drugs for hub genes. 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The qPCR results showed that the expression levels of", "ociated genes in CD. Further verification by qPCR showed that IL-6, PTGS2 and DUOX2 may affect", "l Hospital (Qingdao, China) in October 2022. RT-qPCR was completed in October 2022, and western b", "the five hub genes in CD clinical samples by RT-qPCR All collected clinical tissue samples of CD"], "order_basis": "paper_text_order:1546", "id": "assay:1"}, {"role": "data_generation", "definition_id": "western_blot", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": [". RT-qPCR was completed in October 2022, and western blotting was completed in November 2023 (approval no.", "alyzed by unpaired Student's t-test. For the western blot experiment, the results were analyzed by unp", "was conducted in normal and CD tissues using western blotting (Fig. 8A and B). The protein expression leve"], "order_basis": "paper_text_order:2990", "id": "assay:2"}, {"role": "data_generation", "definition_id": "microarray", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.93, "evidence": ["genes associated with ferroptosis in CD The microarray expression profiling datasets GSE102133 and"], "order_basis": "paper_text_order:3564", "id": "assay:3"}, {"role": "analysis", "definition_id": "group_comparison", "definition_version": "f2132e96ae6c7a4e", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"dsl_catalogue": "f2132e96ae6c7a4e"}, "confidence": 1.0, "evidence": ["In the qPCR experiment, the results were analyzed by unpaired Student's t-test."], "order_basis": "consumes_earlier_output", "id": "assay:4"}]}