Evidence map›Paper›PMID 40373023›Full record

ArticlePloS one2025

Diagnostic, prognostic, and immunological roles of FUT8 in lung adenocarcinoma and lung squamous cell carcinoma.

Zhijun Li, Zhenpeng Zhu, Peng Wang, Chenyang Hou, Lijuan Ren, Dandan Xu, Xiran Wang, Fei Guo, Qingxue Meng, Weizheng Liang and 2 more

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Article
  2. Review
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

12 authors.

Zhijun LiHebei North University, Zhangjiakou City, Hebei Province, China.ORCID https://orcid.org/0009-0005-7399-1065
Zhenpeng ZhuHebei North University, Zhangjiakou City, Hebei Province, China.
Peng WangHebei North University, Zhangjiakou City, Hebei Province, China.
Chenyang HouHebei North University, Zhangjiakou City, Hebei Province, China.
Lijuan RenHebei North University, Zhangjiakou City, Hebei Province, China.
Dandan XuHebei Key Laboratory of Systems Biology and Gene Regulation, Central Laboratory, The First Affiliated Hospital of Hebei North University, Zhangjiakou City, Hebei Province, China.
Xiran WangDepartment of Bioinformatics, School of Health Care, Changchun Vocational College of Health, Changchun City, Jilin Province, China.
Fei GuoDepartment of Surgery, Hebei Key Laboratory of Systems Biology and Gene Regulation, The First Affiliated Hospital of Hebei North University, Zhangjiakou City, Hebei Province, China.
Qingxue MengTechnology Department, The First Affiliated Hospital of Hebei North University, Zhangjiakou City, Hebei Province, China.
Weizheng LiangHebei Key Laboratory of Systems Biology and Gene Regulation, Central Laboratory, The First Affiliated Hospital of Hebei North University, Zhangjiakou City, Hebei Province, China.
Jun XueDepartment of Surgery, Hebei Key Laboratory of Systems Biology and Gene Regulation, The First Affiliated Hospital of Hebei North University, Zhangjiakou City, Hebei Province, China.
Xuejun ZhiDepartment of Respiratory and Critical Care Medicine, The First Affiliated Hospital of Hebei North University, Zhangjiakou City, Hebei Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer remains the leading cause of malignant tumors worldwide in terms of the incidence and mortality, posing a significant threat to human health. Given that distant metastases typically occur at the time of initial diagnosis, leading to a poor 5-year survival rate among patients, it is crucial to identify markers for diagnosis, prognosis, and therapeutic efficacy monitoring. Abnormal glycosylation is a hallmark of cancer cells, characterized by the disruption of core fucosylation, which is predominantly driven by the enzyme fucosyltransferase 8 (FUT8). Evidence indicates that FUT8 is a pivotal enzyme in cancer onset and progression, influencing cellular glycosylation pathways. Utilizing bioinformatics approaches, we have investigated FUT8 in lung cancer, resulting in a more systematic and comprehensive understanding of its role in the disease's pathogenesis. In this study, we employed bioinformatics to analyze the differential expression of FUT8 between LUAD and LUSC. We observed upregulation of FUT8 in both LUAD and LUSC, associated with unfavorable prognosis, and higher diagnostic utility in LUAD. GO/KEGG analysis revealed a primary association between LUAD and the spliceosome. Immunologically, FUT8 expression was significantly associated with immune cell infiltration and immune checkpoint activity, with a notable positive correlation with M2 macrophage infiltration. Our analysis of FUT8 indicates that it may serve as a potential biomarker for lung cancer diagnosis and prognosis, and could represent a therapeutic target for LUAD and LUSC immunotherapy.

Indexed as

Adenocarcinoma of LungCarcinoma, Squamous CellFucosyltransferasesLung NeoplasmsBiomarkers, TumorComputational BiologyFemaleGene Expression Regulation, NeoplasticHumansMalePrognosis3-galactosyl-N-acetylglucosaminide 4-alpha-L-fucosyltransferaseBiomarkers, TumorFucosyltransferases

Identifiers

PMID40373023
PMCPMC12080848

What OpenQuestion 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 OpenQuestion graph.