CSTF2在口腔鳞状细胞癌中的表达及其与免疫浸润及不良预后的关系

IF 3.1 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Frontiers in oral health Pub Date : 2025-02-07 eCollection Date: 2025-01-01 DOI:10.3389/froh.2025.1548829
Zumulaiti Aierken, Muertiza Muhetaer, Zhang Lei, Ainiwaerjiang Abudourousuli
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引用次数: 0

摘要

背景:口腔鳞状细胞癌(OSCC)是一种常见的口腔恶性肿瘤,严重影响患者的生存和生活质量。已知劈裂刺激因子亚单位2 (CSTF2)影响多种癌症类型的肿瘤发展。然而,其与OSCC患者预后和免疫细胞浸润的具体关系尚不清楚。方法:为了评估CSTF2在OSCC中的表达水平和预后意义,我们从癌症基因组图谱(TCGA)中获得了全面的数据,并随后进行了归一化。组织微阵列免疫组化染色分析CSTF2在OSCC样品中的表达。使用Wilcoxon秩和检验评估OSCC和邻近非癌样本之间CSTF2表达的差异。功能富集分析已被用于鉴定与CSTF2相关的生物学途径和功能。采用单样本基因集富集分析(ssGSEA)评估各种免疫细胞浸润与CSTF2表达水平的关系。最终,通过Kaplan-Meier生存分析,结合单因素和多因素Cox回归分析,以及受试者工作特征(ROC)曲线,评估CSTF2的预后意义。结果:在OSCC中观察到CSTF2的高表达,并与不利的临床病理变量相关,包括组织学分级和淋巴结颈部清扫。功能富集分析表明,CSTF2在表皮发育和分化、免疫球蛋白复合物、肽酶和内肽酶抑制剂活性以及细胞色素P450代谢过程中发挥作用。此外,CSTF2的过表达与未成熟树突状细胞(iDCs)、细胞毒性细胞和浆细胞样树突状细胞(pDCs)的浸润呈负相关。值得注意的是,CSTF2表达升高与患者预后降低显著相关。结论:CSTF2在OSCC中表达升高与预后不良相关,这突出了其作为一种创新的预后生物标志物和治疗干预靶点的能力。
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Expression of CSTF2 in oral squamous cell carcinoma and its relationship with immune infiltration and poor prognosis.

Background: Oral squamous cell carcinoma (OSCC) is a prevalent and devastating malignancy of the oral cavity that profoundly affects patient survival and quality of life (QOL). Cleavage Stimulation Factor Subunit 2 (CSTF2) is known to influence tumor development across multiple cancer types. However, its specific association with patient prognosis and immune cell infiltration in OSCC remains insufficiently understood.

Methods: To assess the expression levels and prognostic implications of CSTF2 in OSCC, comprehensive data were acquired from The Cancer Genome Atlas (TCGA) and subsequently normalized. Immunohistochemical staining of tissue microarrays was performed to analyze CSTF2 expression in the OSCC samples. Differences in CSTF2 expression between OSCC and adjacent non-cancerous samples were evaluated using the Wilcoxon rank-sum test. Functional enrichment analyses have been performed to identify biological pathways and functions associated with CSTF2. The relationship between the infiltration of various immune cells and CSTF2 expression levels was assessed using single-sample gene set enrichment analysis (ssGSEA). Ultimately, the prognostic significance of CSTF2 was evaluated through Kaplan-Meier survival analysis, in conjunction with univariate and multivariate Cox regression analyses, as well as receiver operating characteristic (ROC) curves.

Results: High CSTF2 expression was observed in OSCC and associated with unfavorable clinicopathological variables, including histological grade and lymphnode neck dissection. Functional enrichment analysis indicated that CSTF2 plays a role in epidermal development and differentiation, immunoglobulin complexes, peptidases and endopeptidase inhibitor activity, and cytochrome P450 metabolic processes. Additionally, the overexpression of CSTF2 exhibited a negative correlation with the infiltration of immature dendritic cells (iDCs), cytotoxic cells, and plasmacytoid dendritic cells (pDCs). Notably, elevated CSTF2 expression is significantly associated with reduced patient outcomes.

Conclusion: Elevated CSTF2 expression in OSCC is associated with poor prognostic outcomes, highlighting its capacity to function as an innovative prognostic biomarker and a target for therapeutic interventions.

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