Clinical Value of TXNDC12 Combined With IDH and 1p19q as Biomarkers for Prognosis of Glioma.

Pathology oncology research : POR Pub Date : 2021-09-22 eCollection Date: 2021-01-01 DOI:10.3389/pore.2021.1609825
Xinzhuang Wang, Quan Yang, Nan Liu, Qilong Bian, Ming Gao, Xu Hou
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引用次数: 8

Abstract

Background: Glioma is the primary malignant tumor of the central nervous system and presents high mortality and disability rates under existing treatment measures. Thioredoxin domain-containing 12 (TXNDC12) has been shown to play an important role in various malignant tumors. Therefore, we explored the clinicopathological characteristics of TXNDC12 in glioma to bring to light new ideas in its treatment. Methods: We obtained data packages related to TXNDC12 expression status in gliomas from public databases. We analyzed glioma TXNDC12 expression and patient survival status and validated the above results using glioma specimens from our institution. Next, we analyzed the value of TXNDC12 in combination with 1p19q and isocitrate dehydrogenase (IDH) on the prognosis of glioma by regression model and receiver operating characteristic curve (ROC). Finally, we explored the function of related genes by GO analysis and KEGG analysis. Results: Compared with normal brain tissue, the expression of TXNDC12 in glioma cells, regarding both mRNA and protein levels, was significantly upregulated. The survival time of patients with high-expression of TXNDC12 in glioma cells was shortened. In the World Health Organization pathological classification, IDH status, 1p19q status, and IDH combined with 1p19q subgroups, the expression of TXNDC12 increased with the deterioration of the above indicators. Tumor local immune analysis showed that the immune cell infiltration in TXNDC12 high-expressing glioma tissue increased, the tumor purity was reduced. GO and KEGG analyses indicated that TXNDC12 may be involved in the malignant prognosis of glioma through glycosylation and antigen processing and presentation. Conclusion: We showed that TXNDC12 is significantly highly expressed in gliomas. This high expression predicts the poor prognosis of glioma patients and is related to the gliomas’ local immune microenvironment. As a tumor-related gene, TXNDC12 may be used as a new prognostic judgment molecule.

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TXNDC12联合IDH和1p19q作为胶质瘤预后生物标志物的临床价值
背景:胶质瘤是中枢神经系统的原发性恶性肿瘤,在现有的治疗措施下具有很高的死亡率和致残率。含硫氧还蛋白结构域12 (TXNDC12)已被证明在多种恶性肿瘤中发挥重要作用。因此,我们探讨TXNDC12在胶质瘤中的临床病理特点,为其治疗提供新的思路。方法:从公开数据库中获取与胶质瘤中TXNDC12表达状态相关的数据包。我们分析了胶质瘤TXNDC12的表达和患者的生存状况,并使用我们机构的胶质瘤标本验证了上述结果。接下来,我们通过回归模型和受试者工作特征曲线(ROC)分析TXNDC12联合1p19q和异柠檬酸脱氢酶(IDH)对胶质瘤预后的影响。最后,我们通过GO分析和KEGG分析探讨了相关基因的功能。结果:与正常脑组织相比,神经胶质瘤细胞中TXNDC12的mRNA和蛋白表达水平均显著上调。神经胶质瘤细胞中高表达TXNDC12的患者生存时间缩短。在世界卫生组织病理分类、IDH状态、1p19q状态、IDH合并1p19q亚组中,TXNDC12的表达随着上述指标的恶化而升高。肿瘤局部免疫分析显示,TXNDC12高表达胶质瘤组织免疫细胞浸润增加,肿瘤纯度降低。GO和KEGG分析提示TXNDC12可能通过糖基化、抗原加工和递呈参与胶质瘤的恶性预后。结论:我们发现TXNDC12在胶质瘤中显著高表达。这种高表达预示着胶质瘤患者预后不良,并与胶质瘤的局部免疫微环境有关。TXNDC12作为一种肿瘤相关基因,可能作为一种新的预后判断分子。
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