Evidence map›Paper›PMID 40098960›Full record

ArticleFrontiers in immunology2025

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

Lihong Chen, Youfu He, Menghui Duan, Tianwen Yang, Yin Chen, Bo Wang, Dejun Cui, Chen Li

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

24 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Lihong Chen *Department of Gastroenterology, Guizhou Provincial People's Hospital, Guiyang, Guizhou, China.
Youfu He *Department of Cardiology, Guizhou Provincial People's Hospital, Guiyang, Guizhou, China.
Menghui DuanDepartment of Critical Care Medicine, The First Hospital of China Medical University, Shenyang, Liaoning, China.
Tianwen YangDepartment of Orthopaedics, Guizhou Second People's Hospital, Guiyang, Guizhou, China.
Yin ChenDepartment of Gastroenterology, Guizhou Provincial People's Hospital, Guiyang, Guizhou, China.
Bo WangDepartment of General Surgery, Guizhou Provincial People's Hospital, Guiyang, Guizhou, China.
Dejun CuiDepartment of Gastroenterology, Guizhou Provincial People's Hospital, Guiyang, Guizhou, China.
Chen LiDepartment of Pharmacy, the First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

NeoplasmsNuclear Pore Complex ProteinsStomach NeoplasmsBiomarkers, TumorDisease ProgressionGene Expression Regulation, NeoplasticHumansMultiomicsPrognosisTumor MicroenvironmentBiomarkers, TumorNuclear Pore Complex Proteinsgastric cancerimmuneimmune cell infiltrationNup62pan cancer

Identifiers

PMID40098960
PMCPMC11911477

What Socratic holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.