Exploring NUP62's role in cancer progression, tumor immunity, and treatment response: insights from multi-omics analysis.

IF 5.9 2区 医学 Q1 IMMUNOLOGY Frontiers in Immunology Pub Date : 2025-03-03 eCollection Date: 2025-01-01 DOI:10.3389/fimmu.2025.1559396
Lihong Chen, Youfu He, Menghui Duan, Tianwen Yang, Yin Chen, Bo Wang, Dejun Cui, Chen Li
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Abstract

Background: NUP62, a key component of the nuclear pore complex, is closely associated with cellular functions and cancer progression. However, its expression patterns, prognostic value, and relationship with tumour immunity and drug sensitivity across multiple cancers have not been systematically studied. This study used multi-omics analyses combined with experimental validation in gastric cancer to investigate the expression, functional characteristics, and clinical relevance of NUP62 in cancer.

Methods: Data from TCGA, GTEx, and CPTAC databases were used to analyse the expression, mutation characteristics, and clinical associations of NUP62. Tools such as SangerBox, TIMER 2.0, and GSEA were employed to evaluate the relationship between NUP62 and the tumour immune microenvironment, as well as its involvement in signalling pathways. Immunohistochemistry and RT-PCR were used to validate the expression of NUP62 in gastric cancer tissues. PRISM and CTRP databases were utilised to assess the correlation between NUP62 expression and drug sensitivity.

Results: NUP62 was significantly upregulated in multiple cancers and was associated with poor prognosis in cancers such as clear cell renal carcinoma (KIRC), lower-grade glioma (LGG), and adrenocortical carcinoma (ACC), while playing a protective role in others, such as bladder cancer (BLCA) and stomach cancer (STAD). Functional analyses showed that NUP62 is involved in cell cycle regulation, DNA damage repair, and tumour immunity. High NUP62 expression was significantly correlated with increased infiltration of immune cells, such as macrophages and T cells, and a higher response rate to immunotherapy. Drug sensitivity analysis identified NUP62 as a marker of sensitivity to various chemotherapeutic agents. Validation experiments demonstrated that NUP62 mRNA and protein levels were significantly higher in gastric cancer tissues than in adjacent normal tissues.

Conclusions: NUP62 plays a critical role in multiple cancers and shows potential as a biomarker for cancer diagnosis, prognosis, and therapeutic response prediction. Its role in tumour immunity and signalling pathways highlights its potential as a target for immunotherapy and precision medicine.

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探索 NUP62 在癌症进展、肿瘤免疫和治疗反应中的作用:多组学分析的启示。
背景:NUP62是核孔复合物的关键组成部分,与细胞功能和癌症进展密切相关。然而,在多种癌症中,其表达模式、预后价值以及与肿瘤免疫和药物敏感性的关系尚未得到系统研究。本研究采用多组学分析与实验验证相结合的方法,探讨NUP62在胃癌中的表达、功能特征及其临床意义。方法:利用TCGA、GTEx和CPTAC数据库的数据分析NUP62的表达、突变特征及其临床相关性。使用SangerBox、TIMER 2.0和GSEA等工具来评估NUP62与肿瘤免疫微环境之间的关系,以及其参与的信号通路。应用免疫组织化学和RT-PCR验证NUP62在胃癌组织中的表达。利用PRISM和CTRP数据库评估NUP62表达与药物敏感性的相关性。结果:NUP62在透明细胞肾癌(KIRC)、低级别胶质瘤(LGG)、肾上腺皮质癌(ACC)等多种癌症中表达显著上调,与不良预后相关,而在膀胱癌(BLCA)、胃癌(STAD)等其他癌症中则发挥保护作用。功能分析表明,NUP62参与细胞周期调节、DNA损伤修复和肿瘤免疫。NUP62的高表达与免疫细胞(如巨噬细胞和T细胞)的浸润增加以及免疫治疗的高应答率显著相关。药物敏感性分析发现NUP62是对各种化疗药物敏感性的标志。验证实验表明,胃癌组织中NUP62 mRNA和蛋白水平明显高于癌旁正常组织。结论:NUP62在多种癌症中发挥关键作用,具有作为癌症诊断、预后和治疗反应预测的生物标志物的潜力。它在肿瘤免疫和信号通路中的作用突出了它作为免疫治疗和精准医学靶点的潜力。
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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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