ORIGINAL RESEARCH article
Front. Immunol.
Sec. Cancer Immunity and Immunotherapy
Volume 16 - 2025 | doi: 10.3389/fimmu.2025.1613688
This article is part of the Research TopicExploring immune low-response states through single-cell technologies and spatial transcriptomicsView all 8 articles
The Functional and Clinical Significance of Nucleoporin NUP153 Across Human Cancers: A Systematic Study Based on Multi-Omics Analysis and Bench Work Validation
Provisionally accepted- 1Guizhou University, Guiyang, Guizhou Province, China
- 2Guizhou Provincial People's Hospital, Guiyang, China
- 3the First People's Hospital of Zhengzhou, Zhengzhou, China
- 4the fifth clinical medical college of henan university of chinese medicine (zhengzhou people's hospital), Zhengzhou, Henan Province, China
- 5The First Affiliated Hospital of China Medical University, Shenyang, Liaoning Province, China
- 6The People’s Hospital of Gaozhou, Gaozhou, China
- 7Deparment of Pharmacy, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Region, China
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Cancer is a group of highly heterogeneous malignant diseases, and early diagnosis plays a crucial role in improving patient outcomes. Nucleoporins, including Nucleoporin (NUP)153, are involved in key cellular processes such as nucleocytoplasmic transport and cell cycle regulation. However, the role of NUP153 in cancer, especially its expression patterns, mutations, diagnostic value, and relationship with the tumour immune microenvironment, remains insufficiently explored.This study analysed NUP153 expression data from public databases such as TCGA and GTEx. Expression differences between tumour and normal tissues were assessed using Wilcoxon signed-rank tests. Gene set enrichment analysis (GSEA) was used to identify the biological functions and pathways related to NUP153. The relationship between NUP153 expression and immune cell infiltration was evaluated using the TIMER database, while drug sensitivity data were obtained from the GDSC and CTRP databases. Additionally, NUP153 expression in gastric cancer tissues was validated using immunohistochemistry and RT-qPCR.NUP153 showed significant expression variation across cancers, with high levels in cholangiocarcinoma, colorectal cancer, and head and neck squamous cell carcinoma.In gastric cancer, NUP153 was markedly upregulated compared to adjacent noncancerous tissues. High NUP153 expression was linked to tumour-associated macrophage infiltration and correlated with poor prognosis in some cancers like Kidney Renal Papillary Cell Carcinoma and Sarcoma. Drug genomics analysis revealed that NUP153 expression predicted chemotherapy resistance, with imatinib and 4.5dianilinophthalimide showing potential for inhibition in multiple cancers. Single-cell analysis and spatial transcriptomics further revealed that NUP153 expression drives proliferative states in mucus-producing cells in gastric cancer, and its expression was associated with immune cell infiltration patterns, particularly neutrophil and macrophage distribution in the tumour microenvironment.Our findings indicate that NUP153 is a critical factor in multiple cancers, especially gastric cancer, where its elevated expression holds promise as a diagnostic and prognostic biomarker. The results indicate that NUP153 plays a key role in modulating the immune microenvironment and driving tumour progression, positioning it as a potential target for future therapeutic interventions. However, additional studies are required to elucidate the specific molecular mechanisms underlying NUP153's function in cancer and to explore its clinical applicability.
Keywords: NUP153, gastric cancer, tumour immune microenvironment, Chemotherapy sensitivity, prognostic biomarker
Received: 17 Apr 2025; Accepted: 05 Jun 2025.
Copyright: © 2025 He, Wang, Wang, Duan, Zhou, Huang, Wu, Wu and Li. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Youfu He, Guizhou University, Guiyang, 550025, Guizhou Province, China
Feichang Wu, The People’s Hospital of Gaozhou, Gaozhou, 525200, China
Chen Li, Deparment of Pharmacy, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Region, China
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