Sun Annan, Sun Luna, Wu Hao, Li Pu
Clinical College of Central Hospital of Obstetrics and Gynecology, Tianjin Medical University, Tianjin 300000; Department of Gynecology, Tianjin Central Hospital of Gynecology Obstetrics, Tianjin 300052, China.
Department of Gynecology, Tianjin Central Hospital of Gynecology Obstetrics, Tianjin 300052; School of Medicine, Nankai University, Tianjin 300071, China.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2025 Aug;41(8):706-716.
Objective TXN is a thioredoxin (TXN) that participates in many redox reactions and plays a crucial role in various signaling pathways. However, the role of TXN in many cancers is still unclear. The objective of this study is to investigate and visualize the diagnostic, prognostic, and immunological implications of TXN expression across various cancer types. Methods The clinical data were downloaded from the cancer genome mapping project(TCGA) database to analyze the expression level of TXN in pan cancer, and the expression level was preliminarily verified by human protein mapping (HPA)(https://www.proteinatlas.org/)database. The ESTIMATE algorithm and CIBERSORT algorithm were applied to calculate the correlation between TXN expression and immune cell infiltration. The correlation between TXN and microsatellite instability (MSI) and tumor mutation burden (TMB) was analyzed using Spearman method. Gene Set Enrichment Analysis (GSEA) is used for gene biology functional analysis and sensitivity analysis of genes to pan cancer therapeutic drugs. Results TXN is highly expressed in most malignant tumors. The high expression of TXN is associated with overall survival (OS), disease-specific survival (DSS), disease-free interval (DFI), and progression free interval (PFI) in various cancers. Moreover, TXN expression is associated with TMB, MSI, tumor microenvironment, chemotherapy sensitivity and so on. Conclusion TXN may become a potential prognostic biomarker in pan cancer, providing strong theoretical basis for future tumor diagnosis and prognosis judgment. The retinoic acid-inducible gene-I (RIG-I)-like receptor signaling pathway, Toll-like receptor (TLR) signaling pathway, and nucleotide binding oligomerization domain (NOD)-like receptor signaling pathway may be crucial pathways through which TXN influences tumor immunity.
目的硫氧还蛋白(TXN)是一种参与多种氧化还原反应并在各种信号通路中起关键作用的硫氧还蛋白。然而,TXN在许多癌症中的作用仍不清楚。本研究的目的是调查并可视化TXN在各种癌症类型中的表达对诊断、预后和免疫的影响。方法从癌症基因组图谱计划(TCGA)数据库下载临床数据,以分析TXN在泛癌中的表达水平,并通过人类蛋白质图谱(HPA)(https://www.proteinatlas.org/)数据库初步验证该表达水平。应用ESTIMATE算法和CIBERSORT算法计算TXN表达与免疫细胞浸润之间的相关性。使用Spearman方法分析TXN与微卫星不稳定性(MSI)和肿瘤突变负荷(TMB)之间的相关性。基因集富集分析(GSEA)用于基因生物学功能分析以及基因对泛癌治疗药物的敏感性分析。结果TXN在大多数恶性肿瘤中高表达。TXN的高表达与各种癌症的总生存期(OS)、疾病特异性生存期(DSS)、无病间期(DFI)和无进展生存期(PFI)相关。此外,TXN表达与TMB、MSI、肿瘤微环境、化疗敏感性等相关。结论TXN可能成为泛癌中一种潜在的预后生物标志物,为未来肿瘤诊断和预后判断提供有力的理论依据。视黄酸诱导基因-I(RIG-I)样受体信号通路、Toll样受体(TLR)信号通路和核苷酸结合寡聚化结构域(NOD)样受体信号通路可能是TXN影响肿瘤免疫的关键通路。