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pmid:38204239

Differential Gene Expression and Immune Cell Infiltration in Patients with Steroid-induced Necrosis of the Femoral Head.

Guowu Ren · Jie Han · Jian Mo · Zhiwei Xu · Xinjian Feng · Feng Chen · Yukun Wu · Qinglin Peng

Endocrine, metabolic & immune disorders drug targets · 2024 doi:10.2174/0118715303266951231206114153

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:38204239
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science-record
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paper object · 10 fields
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title
Differential Gene Expression and Immune Cell Infiltration in Patients with Steroid-induced Necrosis of the Femoral Head.
doi
10.2174/0118715303266951231206114153
pmid
38204239
authors array · 8 items
[0]
Guowu Ren
[1]
Jie Han
[2]
Jian Mo
[3]
Zhiwei Xu
[4]
Xinjian Feng
[5]
Feng Chen
[6]
Yukun Wu
[7]
Qinglin Peng
journal
Endocrine, metabolic & immune disorders drug targets
year
2024
abstract
OBJECTIVE: The study aimed to study the differential gene expression and immune cell infiltration in patients with steroid-induced necrosis of the femoral head (SANFH), identify the key genes and immune cells of SANFH, and explore the relationship between immune cells and SANFH. METHODS: The high-throughput gene chip dataset GSE123568 was downloaded from the GEO database, and the differential gene expression was analyzed with the R language. The STRING database and Cytoscape software were used to analyze the protein interaction network and screen key genes, and enrichment analysis was carried out on key genes. The infiltration of immune cells in SANFH patients was analyzed and verified by immunohistochemistry. RESULTS: EP300, TRAF6, STAT1, JAK1, CASP8, and JAK2 are key genes in the pathogenesis of SANFH, which mainly involve myeloid cell differentiation, cytokine-mediated signaling pathway, tumor necrosis factor-mediated signaling pathway, and cellular response to tumor necrosis factor through JAK-STAT, NOD-like receptor, toll-like receptor, and other signaling pathways, leading to the occurrence of diseases; immune infiltration and immunohistochemical results have shown the expression of memory B cells and activated dendritic cells as reduced in SANFH patients, while in the same SANFH samples, M1 macrophages have been positively correlated with monocytes, and neutrophils have been negatively correlated with monocytes expression. CONCLUSION: EP300, TRAF6, STAT1, JAK1, CASP8, and JAK2 have exhibited significant differences in SANFH (spontaneous osteonecrosis of the femoral head). Memory B cells, activated dendritic cells, M1 macrophages, monocytes, and neutrophils have shown abnormal expression in SANFH.
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A paired t-test was used to analyze the phenotypic differences between groups and estimate the relationship between each genotype and the risk of SANFH.
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sections[13] "Statistical Analysis" paragraph 2
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A paired t-test was used to analyze the phenotypic differences between groups and estimate the relationship between each genotype and the risk of SANFH.
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sections[38] "AVAILABILITY OF DATA AND MATERIALS" paragraph 2
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The data, used in this study can be obtained from the corresponding author upon request.
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The results showed that compared to healthy controls, SANFH patients had a total of 1836 significantly altered genes, of which 1088 were up-regulated and 748 were down-regulated.
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sections[15] "Analysis of SANFH Differential Genes" paragraph 2
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The results showed that compared to healthy controls, SANFH patients had a total of 1836 significantly altered genes, of which 1088 were up-regulated and 748 were down-regulated.
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The results showed that compared to healthy controls, SANFH patients had a total of 1836 significantly altered genes, of which 1088 were up-regulated and 748 were down-regulated.
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title
Identification of Potential Biomarkers for Improving the Precision of Early Detection of Steroid-induced Osteonecrosis of the Femoral Head
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Automated Assays Laravel application and simulated adapters
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SANFH patients was analyzed and verified by immunohistochemistry. RESULTS: EP300, TRAF6, STAT1, JAK1, CASP8,
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Complete file
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The STRING database and Cytoscape software were used to analyze the protein interaction network and screen key genes, and enrichment analysis was carried out on key genes. The infiltration of immune cells in SANFH patients was analyzed and verified by immunohistochemistry.\nRESULTS: EP300, TRAF6, STAT1, JAK1, CASP8, and JAK2 are key genes in the pathogenesis of SANFH, which mainly involve myeloid cell differentiation, cytokine-mediated signaling pathway, tumor necrosis factor-mediated signaling pathway, and cellular response to tumor necrosis factor through JAK-STAT, NOD-like receptor, toll-like receptor, and other signaling pathways, leading to the occurrence of diseases; immune infiltration and immunohistochemical results have shown the expression of memory B cells and activated dendritic cells as reduced in SANFH patients, while in the same SANFH samples, M1 macrophages have been positively correlated with monocytes, and neutrophils have been negatively correlated with monocytes expression.\nCONCLUSION: EP300, TRAF6, STAT1, JAK1, CASP8, and JAK2 have exhibited significant differences in SANFH (spontaneous osteonecrosis of the femoral head). 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