Department of Neurosurgery, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, PR China; Department of Neurosurgery, West China Hospital of Sichuan University, Chengdu, PR China.
Department of Neurosurgery, West China Hospital of Sichuan University, Chengdu, PR China.
Brain Res Bull. 2021 Oct;175:26-36. doi: 10.1016/j.brainresbull.2021.07.013. Epub 2021 Jul 16.
Low-grade gliomas (LGGs) are slow-growing brain cancer in central nervous system neoplasms. EMILIN2 is an extracellular matrix (ECM) protein which could influence the progress of some tumour which is unclear in LGG. In our study, the methylation, expression, prognosis and immune value of EMILIN2 in LGG were analysed through bioinformatics analysis. We analysed the LGG data from The Cancer Genome Atlas (TCGA) and discovered that the EMILIN2 expression, negatively correlated to the EMILIN2 methylation, could predict a poor prognosis and was associated with different clinical parameters. Moreover, univariate and multivariate Cox regression were performed in CGGA, which showed that the EMILIN2 could be an independent prognostic biomarker in LGG. Moreover, EMILIN2 expression showed a correlation with gene makers in some immune cells, which identified the significance of EMILIN2 in immune infiltration. Finally, we used RT-PCR to verify the EMILIN2 expression level in different grades which showed there were significantly different (P < 0.05). Similarly, high expression of EMILIN2 could predict a poor prognosis (P = 0.0078). In conclusion, EMILIN2 could act as an independent prognostic biomarker which might be associated with the malignancy and development of gliomas and play a crucial role in glioma in immune infiltration.
低级别胶质瘤 (LGGs) 是中枢神经系统肿瘤中生长缓慢的脑癌。EMILIN2 是一种细胞外基质 (ECM) 蛋白,其在 LGG 中的作用尚不清楚。在我们的研究中,通过生物信息学分析,分析了 EMILIN2 在 LGG 中的甲基化、表达、预后和免疫价值。我们分析了来自癌症基因组图谱 (TCGA) 的 LGG 数据,发现 EMILIN2 的表达与 EMILIN2 的甲基化呈负相关,可预测不良预后,并与不同的临床参数相关。此外,在 CGGA 中进行了单因素和多因素 Cox 回归分析,表明 EMILIN2 可以作为 LGG 的独立预后生物标志物。此外,EMILIN2 表达与某些免疫细胞中的基因标志物相关,这表明 EMILIN2 在免疫浸润中的重要性。最后,我们使用 RT-PCR 验证了不同级别之间的 EMILIN2 表达水平,结果显示存在显著差异 (P < 0.05)。同样,EMILIN2 的高表达可预测不良预后 (P = 0.0078)。总之,EMILIN2 可以作为独立的预后生物标志物,可能与胶质瘤的恶性程度和发展有关,并在胶质瘤的免疫浸润中发挥关键作用。