[Bioinformatic analysis of the clinical significance of calneuron 1 (CALN1) in glioma and its correlation with immune cell infiltration].

胶质瘤 异柠檬酸脱氢酶 免疫系统 生物 癌症研究 生存分析 临床意义 基因表达 渗透(HVAC) 基因 肿瘤科 医学 内科学 免疫学 生物化学 物理 热力学
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Han Zhang,Jinhao Zhang,Tao Wang
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期刊:PubMed 卷期号:39 (3): 205-212
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Objective To analyze the clinical significance of calneuron 1 (CALN1) expression in glioma and its role in tumor immune cell infiltration by bioinformatics. Methods The expression of CALN1 gene in glioma in the Cancer Genome Atlas (TCGA) database was analyzed by Xiantao Academic Online. Kaplan-Meier survival analysis was used to evaluate its prognostic value, and receiver operating characteristic (ROC) curve was employed to evaluate its clinical diagnostic efficiency. Gene Set Enrichment Analysis (GSEA) was adopted to identify the potential mechanism of CALN1 in glioma. The relationship between CALN1 mRNA and glioma immune cell infiltration was discussed. Results The expression of CALN1 decreased significantly in glioma, and its expression level was negatively correlated with tumor grade. Compared with the control group, the expression level of CALN1 in isocitrate dehydrogenase mutant and 1p/19q co-deletion gliomas increased significantly. Glioma patients with low expression of CALN1 had poor prognosis and significantly reduced overall survival, disease specific survival and progression-free interval. ROC curve analysis showed that CALN1 expression level had good clinical diagnostic value. The results of GSEA gene enrichment suggested that the expression level of CALN1 was negatively correlated with mitosis and neutrophil degranulation. Immunoinfiltration analysis showed that T helper type 2 (Th2) cells, macrophages and neutrophils were significantly increased in the group with low expression of CALN1. Conclusion The expression level of CALN1 in glioma is positively correlated with the prognosis. The abnormal decrease of CALN1 expression may lead to the invasion of tumor-promoting immune cells. CALN1 can be used as a potential prognostic marker and therapeutic target for glioma.

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