Bioinformatics Analysis of the Key Genes and Pathways in Multiple Myeloma

被引:0
|
作者
Sheng, Xinge [1 ,2 ]
Wang, Shuo [2 ]
Huang, Meijiao [1 ]
Fan, Kaiwen [1 ,2 ]
Wang, Jiaqi [1 ,2 ]
Lu, Quanyi [1 ,2 ]
机构
[1] Xiamen Univ, Zhongshan Hosp, Dept Hematol, Xiamen, Peoples R China
[2] Xiamen Univ, Sch Med, Clin Med Dept, Xiamen, Peoples R China
关键词
multiple myeloma; bioinformatics; RT qPCR; PPI; PI3K/AKT SIGNALING PATHWAY; BONE; DIFFERENTIATION; INHIBITION;
D O I
10.2147/IJGM.S377321
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To study the differentially expressed genes between multiple myeloma and healthy whole blood samples by bioinfor-matics analysis, find out the key genes involved in the occurrence, development and prognosis of multiple myeloma, and analyze and predict their functions.Methods: The gene chip data GSE146649 was downloaded from the GEO expression database. The gene chip data GSE146649 was analyzed by R language to obtain the genes with different expression in multiple myeloma and healthy samples, and the cluster analysis heat map was constructed. At the same time, the protein-protein interaction (PPI) networks of these DEGs were established by STRING and Cytoscape software. The gene co-expression module was constructed by weighted correlation network analysis (WGCNA). The hub genes were identified from key gene and central gene. TCGA database was used to analyze the expression of differentially expressed genes in patients with multiple myeloma. Finally, the expression level of TNFSF11 in whole blood samples from patients with multiple myeloma was analyzed by RT qPCR.Results: We identified four genes (TNFSF11, FGF2, SGMS2, IGFBP7) as hub genes of multiple myeloma. Then, TCGA database was used to analyze the survival of TNFSF11, FGF2, SGMS2 and IGFBP7 in patients with multiple myeloma. Finally, the expression level of TNFSF11 in whole blood samples from patients with multiple myeloma was analyzed by RT qPCR.Conclusion: The study suggests that TNFSF11, FGF2, SGMS2 and IGFBP7 are important research targets to explore the pathogen-esis, diagnosis and treatment of multiple myeloma.
引用
收藏
页码:6999 / 7016
页数:18
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