Evidence map›Paper›PMID 39806429›Full record

ArticleJournal of translational medicine2025

Identification and validation of the important role of KIF11 in the development and progression of endometrial cancer.

Biying Wang, Lunmin Bao, Xiaoduo Li, Guang Sun, Wu Yang, Nanzi Xie, Ling Lei, Wei Chen, Hailong Zhang, Man Chen and 4 more

Abstract readValidation Study
In one paragraph

Article in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
  2. Review
  3. FTO-modulated mJournal of translational medicine · 2026
    Article
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  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Kinesin Spindle Protein (KIF11) in Mitosis and Cancer.International journal of molecular sciences · 2025
    Review
  11. Article
  12. Plin2 Coordinates Immune and Metabolic Reprogramming in Lacrimal Gland Aging.Investigative ophthalmology & visual science · 2025
    Article
  13. Article
  14. Article
  15. Article
  16. Article
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

14 authors.

Biying Wang *School of Clinical Laboratory Science, Guizhou Medical University, Guiyang, Guizhou, 550000, China.
Lunmin Bao *School of Clinical Laboratory Science, Guizhou Medical University, Guiyang, Guizhou, 550000, China.
Xiaoduo LiDepartment of Laboratory Medicine, Peoples' Hospital of Anshun City, Guizhou, 561000, Anshun, China.
Guang SunDepartment of Laboratory Medicine, Peoples' Hospital of Anshun City, Guizhou, 561000, Anshun, China.
Wu YangDepartment of Gynaecology, Peoples' Hospital of Anshun City, Guizhou, 561000, Anshun, China.
Nanzi XieDepartment of Pathology, Peoples' Hospital of Anshun City, Guizhou, 561000, Anshun, China.
Ling LeiDepartment of Gynaecology, Peoples' Hospital of Anshun City, Guizhou, 561000, Anshun, China.
Wei ChenDepartment of Pathology, Peoples' Hospital of Anshun City, Guizhou, 561000, Anshun, China.
Hailong ZhangDepartment of Laboratory Medicine, Peoples' Hospital of Anshun City, Guizhou, 561000, Anshun, China.
Man ChenDepartment of Gynaecology, Peoples' Hospital of Anshun City, Guizhou, 561000, Anshun, China.
Xing ZhaoSchool of Clinical Laboratory Science, Guizhou Medical University, Guiyang, Guizhou, 550000, China.
Xiufang WanSchool of Clinical Laboratory Science, Guizhou Medical University, Guiyang, Guizhou, 550000, China.
Rui YuanSchool of Clinical Laboratory Science, Guizhou Medical University, Guiyang, Guizhou, 550000, China.
Hongmei JiangSchool of Clinical Laboratory Science, Guizhou Medical University, Guiyang, Guizhou, 550000, China. jianghongmei@gmc.edu.cn.ORCID 0000-0001-7427-5566

Funding

Anshun Science and Technology Plan Project Anshikeshe [2024]03National Natural Science Foundation of China 81960393project of Natural Science Research Innovation Group of General Undergraduate College in Guizhou Province Qianjiaohe KY character [2021]016
6 · The paper itself

Abstract

backgroundHuman kinesin family member 11 (KIF11) plays a vital role in regulating the cell cycle and is implicated in the tumorigenesis and progression of various cancers, but its role in endometrial cancer (EC) is still unclear. Our current research explored the prognostic value, biological function and targeting strategy of KIF11 in EC through approaches including bioinformatics, machine learning and experimental studies.

methodsThe GSE17025 dataset from the GEO database was analyzed via the limma package to identify differentially expressed genes (DEGs) in EC. Functional enrichment analysis of the DEGs was conducted using Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses. DEGs were further screened for hub genes through protein-protein interaction (PPI) network analysis and machine learning. The role of the hub gene KIF11 in EC was analyzed using clinical data from the TCGA database. The expression of KIF11 in EC was subsequently validated in clinical samples. In vitro experiments were utilized to evaluate the effects of KIF11 on biological functions such as proliferation, migration, apoptosis, and the cell cycle in endometrial cancer cells.

resultsA total of 877 DEGs, which are widely involved in important biological processes such as cell division, tubulin binding, and the cell cycle, were identified. Through PPI network analysis and machine learning, KIF11 was selected as the hub gene for subsequent analysis and experimental validation. An analysis of TCGA data revealed that KIF11 is highly expressed in EC and is associated with tumor grade, stage, and a low survival rate. The overexpression of KIF11 in tumor tissues was further confirmed in EC patient samples. KIF11 knockdown had inhibitory effects on cell proliferation, migration and invasion. Flow cytometry analysis revealed that KIF11 knockdown induced G2/M phase arrest and promoted apoptosis in EC cells.

conclusionOur study demonstrated that KIF11 was upregulated in EC and was strongly associated with a poor prognosis. Notably, we found that reduced KIF11 expression inhibited EC cell proliferation, migration and invasion. KIF11 knockdown caused more EC cells to arrest in the G2/M phase and undergo apoptosis. The findings of our study emphasized that KIF11 may be a promising prognostic biomarker and therapeutic target for EC patients.

Indexed as

Disease ProgressionEndometrial NeoplasmsKinesinsApoptosisCarcinogenesisCell CycleCell Line, TumorCell MovementCell ProliferationComputational BiologyFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGene OntologyGene Regulatory NetworksHumansKIF11 protein, humanKinesinsBioinformaticsEndometrial cancerKIF11Machine learning

Identifiers

PMID39806429
PMCPMC11727483

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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.