Xin-Yang Qu, Yong Xu, Rui-Min Wu, Gao-Chun Xiao, Ping-Feng Wang, Jin Xie, Xu-Sheng Liu
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Additionally, the regulatory mechanisms of ULBP2 were explored by investigations of promoter DNA methylation, m6A regulation, and immune cell infiltration. Finally, cellular experiments were conducted to evaluate ULBP2 as a potential biomarker to predict CRC progression.</p><p><strong>Results: </strong>ULBP2 upregulation was significantly correlated with an advanced pathological stage of CRC. ROC curve analysis indicated that ULBP2 has strong diagnostic value. Kaplan-Meier survival analysis showed that high ULBP2 expression was predictive of a poorer prognosis. Cox regression analysis highlighted ULBP2 as an independent prognostic factor. ULBP2 expression was linked to promoter methylation, m6A regulation, and immune cell infiltration. Cellular experiments showed that ULBP2 knockdown suppressed CRC progression.</p><p><strong>Conclusion: </strong>ULBP2 has potential as a prognostic biomarker and therapeutic target of CRC. 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引用次数: 0
摘要
背景:ul16结合蛋白2 (ULBP2)是参与自然杀伤细胞活化和肿瘤免疫监视的重要免疫调节分子,但其在结直肠癌(CRC)中的具体作用和临床意义有待进一步探讨。方法:使用The Cancer Genome Atlas和Gene expression Omnibus数据库分析CRC与正常组织中ULBP2的表达,以及与临床病理特征的潜在关联,同时通过受试者工作特征(ROC)曲线评估诊断价值,并通过Kaplan-Meier和Cox回归分析评估预后影响。此外,通过对启动子DNA甲基化、m6A调控和免疫细胞浸润的研究,探讨了ULBP2的调控机制。最后,进行细胞实验来评估ULBP2作为预测结直肠癌进展的潜在生物标志物。结果:ULBP2表达上调与结直肠癌的晚期病理阶段显著相关。ROC曲线分析表明ULBP2具有较强的诊断价值。Kaplan-Meier生存分析显示,ULBP2高表达预示预后较差。Cox回归分析显示ULBP2是一个独立的预后因素。ULBP2的表达与启动子甲基化、m6A调控和免疫细胞浸润有关。细胞实验表明,ULBP2敲低可抑制结直肠癌的进展。结论:ULBP2具有作为结直肠癌预后生物标志物和治疗靶点的潜力。这些发现为今后的肿瘤发生机制研究和临床应用提供了有价值的见解。
Integrated multi-omics analysis of UL16-binding protein 2 as a prognostic and immunotherapy biomarker for colorectal cancer.
Background: UL16-binding protein 2 (ULBP2) is an important immune regulatory molecule involved in natural killer cell activation and tumor immune surveillance, although the specific role and clinical significance in colorectal cancer (CRC) require further exploration.
Methods: ULBP2 expression in CRC vs. normal tissues was analyzed using The Cancer Genome Atlas and the Gene Expression Omnibus databases, along with potential associations with clinicopathological features, while the diagnostic value was assessed with receiver operating characteristic (ROC) curves and the prognostic impact by Kaplan-Meier and Cox regression analyses. Additionally, the regulatory mechanisms of ULBP2 were explored by investigations of promoter DNA methylation, m6A regulation, and immune cell infiltration. Finally, cellular experiments were conducted to evaluate ULBP2 as a potential biomarker to predict CRC progression.
Results: ULBP2 upregulation was significantly correlated with an advanced pathological stage of CRC. ROC curve analysis indicated that ULBP2 has strong diagnostic value. Kaplan-Meier survival analysis showed that high ULBP2 expression was predictive of a poorer prognosis. Cox regression analysis highlighted ULBP2 as an independent prognostic factor. ULBP2 expression was linked to promoter methylation, m6A regulation, and immune cell infiltration. Cellular experiments showed that ULBP2 knockdown suppressed CRC progression.
Conclusion: ULBP2 has potential as a prognostic biomarker and therapeutic target of CRC. These findings provide valuable insights for future studies of tumorigenic mechanisms and clinical applications.
期刊介绍:
Functional & Integrative Genomics is devoted to large-scale studies of genomes and their functions, including systems analyses of biological processes. The journal will provide the research community an integrated platform where researchers can share, review and discuss their findings on important biological questions that will ultimately enable us to answer the fundamental question: How do genomes work?