Expression of AEBP1 and its prognostic role in glioma based on the data-mining of TCGA and GTEx databases / 西安交通大学学报(医学版)
Journal of Xi'an Jiaotong University(Medical Sciences)
; (6): 503-508, 2022.
Article
in Zh
| WPRIM
| ID: wpr-1011526
Responsible library:
WPRO
ABSTRACT
【Objective】 To explore the expressions of adipocyte enhancer binding protein 1 (AEBP1) gene and its isoforms in different types of gliomas, and the influence of AEBP1 gene on the prognosis of patients with different types of gliomas. 【Methods】 We used the GEPIA2 visual network analysis tool to analyze AEBP1 gene expression levels in the tumor tissues of glioblastomas (GBM, including classical, mesenchymal, neural, and proneural ones) and low-grade gliomas (LGG, including astrocytoma, oligoastrocytoma, oligodendroglioma) in the TCGA database and normal human tissue samples in the TCGA and GTEx databases by one-way ANOVA. The distribution trend of isoforms of AEBP1 gene in gliomas was analyzed using the violin plot. The Kaplan-Meier survival curve was drawn and the Logrank test was used to analyze the influence of AEBP1 gene expression in GBM and LGG tumor tissues on the prognosis of glioma patients. 【Results】 The expression of AEBP1 in the tumor tissues of overall GBM and the four types of GBM was higher than that in the normal control tissues (P<0.05). The expression of AEBP1 in astrocytoma and oligodendrocyte astrocytoma tumor tissues was higher than that in normal control tissues (P<0.05). There were nine isoforms of AEBP1 gene in GBM and LGG, and the expression level in GBM was higher. The overall survival (OS) of the AEBP1 low expression group of GBM patients and the proneuronal GBM patients was better than that of the high expression group (P<0.05). The OS and progression-free survival of LGG patients and the AEBP1 low-expression group of astroglioma were better than those of the high-expression group (P<0.05). 【Conclusion】 AEBP1 has an important clinical value in the pathogenesis and development of GBM and LGG, and thus can be used as a diagnostic marker and a candidate gene for targeted therapy.
Full text:
1
Index:
WPRIM
Language:
Zh
Journal:
Journal of Xi'an Jiaotong University(Medical Sciences)
Year:
2022
Type:
Article