SLC12A9 is an immunological and prognostic biomarker for glioma

IF 2.4 3区 生物学 Q2 GENETICS & HEREDITY Gene Pub Date : 2025-02-10 Epub Date: 2024-11-30 DOI:10.1016/j.gene.2024.149136
Danting Li , Peilin Zheng , Shoujun Huang
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Abstract

Background

Glioma is one of the most common malignant brain tumors. It has a high rate of progression and a poor prognosis, and effective biomarkers still need to be identified. The solute carrier family 12 (SLC12) family has been reported to be involved in various physiological and pathological processes, but their functional roles in glioma remain unclear.

Methods

Using public datasets, we studied the mutation and expression level of SLC12 family genes in glioma and identified the significantly differentially expressed member solute carrier family 12 member 9 (SLC12A9). We further predicted the prognostic role of SLC12A9 in glioma by using the Kaplan–Meier method and Cox regression analysis. Then, we performed biological functional enrichment analysis. We focused on the relationships between SLC12A9 expression and immune infiltration in glioma. Meanwhile, we conducted in vitro experiments to evaluate the effect of SLC12A9 expression on glioma cells.

Results

Among the members of the SLC12 family, SLC12A9 had the highest mutation rate in glioma, with gene amplification as the major mutation type, and its expression was significantly upregulated in glioma. Higher SLC12A9 expression was significantly associated with older age, higher grade, wild-type isocitrate dehydrogenase (IDH), and a worse prognosis. The functional enrichment analysis indicated that SLC12A9 is mainly related to ion channel annotation. Gene set enrichment analysis (GSEA) revealed that SLC12A9 was mainly related to the DNA replication pathway. Furthermore, we found that SLC12A9 correlated with tumor-infiltrating immune cells and immune checkpoints. Thus, SLC12A9 may be involved in regulating the immune response of glioma. Finally, our in vitro experiments revealed that silencing SLC12A9 dramatically inhibited glioma cell growth and migration.

Conclusions

We showed that SLC12A9 may be a new predictive biomarker for glioma diagnosis, prognosis, and immunotherapy response, offering helpful guidelines to advance glioma treatment.
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SLC12A9是胶质瘤的免疫学和预后生物标志物。
背景:神经胶质瘤是最常见的恶性脑肿瘤之一。它的进展率高,预后差,仍然需要确定有效的生物标志物。溶质载体家族12 (SLC12)家族已被报道参与多种生理和病理过程,但其在胶质瘤中的功能作用尚不清楚。方法:利用公开数据集,研究胶质瘤SLC12家族基因的突变及表达水平,鉴定出溶质载体家族12成员9 (SLC12A9)的显著差异表达。我们通过Kaplan-Meier法和Cox回归分析进一步预测SLC12A9在胶质瘤中的预后作用。然后,我们进行了生物功能富集分析。我们关注SLC12A9表达与胶质瘤免疫浸润的关系。同时,我们通过体外实验评估SLC12A9表达对胶质瘤细胞的影响。结果:SLC12家族成员中,SLC12A9在胶质瘤中的突变率最高,以基因扩增为主要突变类型,其在胶质瘤中的表达显著上调。SLC12A9高表达与年龄、高分级、野生型异柠檬酸脱氢酶(IDH)和较差的预后显著相关。功能富集分析表明,SLC12A9主要与离子通道注释有关。基因集富集分析(GSEA)显示SLC12A9主要与DNA复制途径有关。此外,我们发现SLC12A9与肿瘤浸润性免疫细胞和免疫检查点相关。因此,SLC12A9可能参与调节胶质瘤的免疫反应。最后,我们的体外实验表明,沉默SLC12A9可显著抑制胶质瘤细胞的生长和迁移。结论:我们发现SLC12A9可能是胶质瘤诊断、预后和免疫治疗反应的一种新的预测性生物标志物,为推进胶质瘤治疗提供了有益的指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Gene
Gene 生物-遗传学
CiteScore
6.10
自引率
2.90%
发文量
718
审稿时长
42 days
期刊介绍: Gene publishes papers that focus on the regulation, expression, function and evolution of genes in all biological contexts, including all prokaryotic and eukaryotic organisms, as well as viruses.
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