Zhou Min, Li Jinquan, Chen Cheng
College of Medicine, Wuhan University of Science and Technology, Wuhan, China.
Wuhan Asia Heart Hospital, Wuhan, China.
Front Genet. 2022 Jul 15;13:914219. doi: 10.3389/fgene.2022.914219. eCollection 2022.
The ZFP36 Ring Finger Protein Like 2 (ZFP36L2) is an RNA-binding protein that regulates gene expression at post-transcriptional level. However, the clinical significance and prognostic value of ZFP36L2 in lower-grade glioma (LGG) remain unclear. ZFP36L2 expression was investigated using public datasets and the prognostic merit of ZFP36L2 with LGG patients was further evaluated. The correlation between the genetic alteration of ZFP36L2 and its mRNA expression was accessed via cBioPortal. Additionally, the prognostic value of the ZFP36L2 methylation levels in LGG was evaluated by MethSurv. The potential biological role of ZFP36L2 in LGG was identified by performing functional analyses. We also examined the correlation between ZFP36L2 expression and the immune infiltration. Finally, the predictive value of ZFP36L2 to immunotherapy was assessed. ZFP36L2 was highly expressed in LGG patients and overexpressed ZFP36L2 predicted poor clinical outcomes. We further identified ZFP36L2 as an independent prognostic factor. The methylation level of ZFP36L2 negatively correlated with the ZFP36L2 expression, and patients with low ZFP36L2 methylation had worse overall survival. The results of functional analysis indicated that ZFP36L2 was involved in multiple immune response-related pathways in LGG. Furthermore, high expression of ZFP36L2 was significantly and positively correlated with immune infiltration. Finally, we found that ZFP36L2 expression was positively correlated with the immune checkpoint PD-L1, and ZFP36L2 low expression cohort gained better benefit from immunotherapy. Our findings demonstrate that ZFP36L2 is a potential biomarker for LGG, highlighting its potential as a therapeutic target in immunotherapy.
锌指蛋白36环指蛋白样2(ZFP36L2)是一种RNA结合蛋白,可在转录后水平调节基因表达。然而,ZFP36L2在低级别胶质瘤(LGG)中的临床意义和预后价值仍不清楚。本研究利用公共数据集调查ZFP36L2的表达情况,并进一步评估ZFP36L2对LGG患者的预后价值。通过cBioPortal分析ZFP36L2基因改变与其mRNA表达之间的相关性。此外,利用MethSurv评估ZFP36L2甲基化水平在LGG中的预后价值。通过功能分析确定ZFP36L2在LGG中的潜在生物学作用。我们还研究了ZFP36L2表达与免疫浸润之间的相关性。最后,评估ZFP36L2对免疫治疗的预测价值。ZFP36L2在LGG患者中高表达,ZFP36L2过表达预示着不良的临床结局。我们进一步确定ZFP36L2是一个独立的预后因素。ZFP36L2的甲基化水平与ZFP36L2表达呈负相关,ZFP36L2甲基化水平低的患者总生存期较差。功能分析结果表明,ZFP36L2参与了LGG中多个免疫反应相关通路。此外,ZFP36L2的高表达与免疫浸润显著正相关。最后,我们发现ZFP36L2表达与免疫检查点PD-L1呈正相关,并发现ZFP36L2低表达组从免疫治疗中获益更大。我们的研究结果表明,ZFP36L2是LGG的一个潜在生物标志物,突出了其作为免疫治疗靶点的潜力。