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Ferroptosis-related gene model to predict overall survival of papillary thyroid carcinoma

机译:预测甲状腺状癌总生存期的铁死亡相关基因模型

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摘要

Background: Ferroptosis is a form of programmed cell death that is closely associated with the development of various tumors. However, the correlation between ferroptosis and papillary thyroid carcinoma (PTC) is unclear. This study was performed to investigate the expression and prognostic value of ferroptosis-related genes (FRG) in PTC. Methods: mRNA expression profiles and corresponding clinical data of patients with PTC were analyzed to identify factors affecting prognosis. Independent risk factors were used to establish a predictive receiver operating characteristic model. Single-sample gene set enrichment analysis (ssGSEA) was used to evaluate the correlation between ferroptosis and immune cells. Results: Most genes related to FRG (78.8) were differentially expressed between the tumor and adjacent normal tissues. In univariate Cox regression analysis, 12 differentially expressed genes were associated with prognostic survival. We constructed a prognostic model of eight FRG, including DPP4, GPX4, GSS, ISCU, MIOX, PGD, TF, and TFRC, and divided patients into two groups: high and low risk. The high-risk group exhibited a significantly reduced overall survival rate. In multivariate Cox regression analysis, the risk score was used as an independent prognostic factor. ssGSEA showed that immune cell types and their expression in the high- and low-risk groups were significant. Conclusion: This study constructed a prognostic model of ferroptosis-related genes and determined its usefulness as an independent prognostic factor, providing a reference for the treatment and prognosis of patients with PTC.
机译:背景:铁死亡是一种程序性细胞死亡形式,与各种肿瘤的发展密切相关。然而,铁死亡与甲状腺状癌 (PTC) 之间的相关性尚不清楚。本研究旨在探讨铁死亡相关基因(FRG)在PTC中的表达及预后价值。方法:分析PTC患者mRNA表达谱及相应的临床资料,确定影响预后的因素。利用独立危险因素建立预测性受试者工作特征模型。采用单样本基因集富集分析(ssGSEA)评估铁死亡与免疫细胞的相关性。结果:大多数与FRG相关的基因(78.8%)在肿瘤和邻近正常组织之间差异表达。在单因素Cox回归分析中,12个差异表达基因与预后生存期相关。我们构建了DPP4、GPX4、GSS、ISCU、MIOX、PGD、TFRC等8例FRG的预后模型,并将患者分为高危和低危两组。高危组的总生存率显著降低。在多因素Cox回归分析中,风险评分被用作独立的预后因素。ssGSEA显示免疫细胞类型及其在高危组和低危组中的表达显著。结论:本研究构建了铁死亡相关基因的预后模型,并确定了其作为独立预后因素的实用性,为PTC患者的治疗和预后提供参考。

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