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硒蛋白GPX3是胃腺癌和脑低级别胶质瘤的一种新型预后指标:来自综合泛癌分析的证据。

Selenoprotein GPX3 is a novel prognostic indicator for stomach adenocarcinoma and brain low-grade gliomas: Evidence from an integrative pan-cancer analysis.

作者信息

Wang Yuetong, Fu Guotao, Chen Xueqin, Xia Zengrun, Qi Meng, Du Xiaoping, Liu Kun, Liu Qiling, Sun Na, Shi Chuandao, Qu Kai, Zhang Rongqiang

机构信息

Shaanxi Academy of Traditional Chinese Medicine (Shaanxi Provincial Hospital of Chinese Medicine), Xi'an, 710003, PR China.

School of Public Health, Shaanxi University of Chinese Medicine, Xianyang, 712046, PR China.

出版信息

Heliyon. 2024 Jun 1;10(11):e32271. doi: 10.1016/j.heliyon.2024.e32271. eCollection 2024 Jun 15.

Abstract

BACKGROUND

The antioxidant enzyme is a selenoprotein that transports selenium in blood and maintains its levels in peripheral tissues. Aberrant expression is strongly linked to the development of some tumors. However, there is a scarcity of studies examining the pan-cancer expression patterns and prognostic relevance of .

METHODS

expression levels in normal tissues and multiple tumors were analyzed using TCGA, CCLE, GTEx, UALCAN and HPA databases. Forest plots and KM survival curves were utilized to evaluate the correlation between expression and the outcome of tumor patients. The prognostic value of in LGG was assessed utilizing the CGGA datasets, and that in STAD was tested by TCGA and GEO databases. A nomogram was then constructed to predict OS in STAD using R software. Additionally, the impact of on post-chemoradiotherapy OS in patients with LGG and STAD was evaluated using the KM method. The multiplicative interaction of expression, chemotherapy and radiotherapy on STAD and LGG was analyzed using logistic regression models. The correlation of with the immune infiltration, immune neoantigens and MMR genes were investigated in TCGA cohort.

RESULTS

exhibited downregulation across 21 tumor types, including STAD, with its decreased expression significantly associated with improved OS, DFS, PFS and DSS. Conversely, in LGG, low levels of expression were indicative of a poorer prognosis. Univariate and multivariate Cox models further identified as an independent predictor of STAD, and a nomogram based on expression and other independent factors showed high level of predictive accuracy. Moreover, low expression and chemotherapy prolonged the survival of STAD. In LGG patients, chemoradiotherapy, and chemotherapy, and and chemoradiotherapy may improve prognosis. Our observations reveal a notable connection between and immune infiltration, immune neoantigens, and MMR genes.

CONCLUSIONS

The variations in expression are linked to the controlling tumor development and could act as a promising biomarker that impacts the prognosis of specific cancers like STAD and LGG.

摘要

背景

抗氧化酶是一种硒蛋白,可在血液中运输硒并维持其在外周组织中的水平。异常表达与某些肿瘤的发生密切相关。然而,缺乏关于该蛋白的泛癌表达模式及其预后相关性的研究。

方法

使用TCGA、CCLE、GTEx、UALCAN和HPA数据库分析正常组织和多种肿瘤中的该蛋白表达水平。采用森林图和KM生存曲线评估该蛋白表达与肿瘤患者预后的相关性。利用CGGA数据集评估该蛋白在低级别胶质瘤(LGG)中的预后价值,并通过TCGA和GEO数据库在胃癌(STAD)中进行测试。然后使用R软件构建列线图以预测STAD患者的总生存期(OS)。此外,采用KM法评估该蛋白对LGG和STAD患者放化疗后OS的影响。使用逻辑回归模型分析该蛋白表达、化疗和放疗对STAD和LGG的相乘交互作用。在TCGA队列中研究该蛋白与免疫浸润、免疫新抗原和错配修复(MMR)基因的相关性。

结果

该蛋白在包括STAD在内的21种肿瘤类型中均呈下调,其表达降低与OS、无病生存期(DFS)、无进展生存期(PFS)和疾病特异性生存期(DSS)改善显著相关。相反,在LGG中,该蛋白低表达提示预后较差。单因素和多因素Cox模型进一步确定该蛋白为STAD的独立预测因子,基于该蛋白表达和其他独立因素的列线图显示出较高的预测准确性。此外,该蛋白低表达和化疗可延长STAD患者的生存期。在LGG患者中,放化疗、该蛋白与化疗以及该蛋白与放化疗联合可能改善预后。我们的观察结果揭示了该蛋白与免疫浸润、免疫新抗原和MMR基因之间的显著联系。

结论

该蛋白表达的变化与控制肿瘤发展有关,并且可能作为一种有前景的生物标志物,影响STAD和LGG等特定癌症的预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b3a/11170152/9a5413ab82bb/gr1.jpg

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