Evidence map›Paper›PMID 40070823›Full record

ArticleFrontiers in immunology2025

A comprehensive analysis of the prognostic value, expression characteristics and immune correlation of MKI67 in cancers.

Xiaolan Pan, Caibiao Wei, Jingyu Su, Min Fang, Qiumei Lin, Yuling Qin, Jie Gao, Jie Zhao, Huiliu Zhao, Fengfei Liu

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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Cancers · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Evidence for Genotype-Specific Optimal Blood Lead Levels for Cancer Risk:International journal of molecular sciences · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

10 authors.

Xiaolan Pan *Department of Clinical Laboratory, Guangxi Medical University Cancer Hospital, Nanning, China.
Caibiao Wei *Department of Clinical Laboratory, Guangxi Medical University Cancer Hospital, Nanning, China.
Jingyu Su *Genetic Metabolism Center laboratory, Guangxi Zhuang Autonomous Region Maternal and Child Health Care Hospital, Nanning, China.
Min FangDepartment of Clinical Laboratory, Guangxi Medical University Cancer Hospital, Nanning, China.
Qiumei LinDepartment of Clinical Laboratory, Guangxi Medical University Cancer Hospital, Nanning, China.
Yuling QinDepartment of Clinical Laboratory, Guangxi Medical University Cancer Hospital, Nanning, China.
Jie GaoDepartment of Clinical Laboratory, Guangxi Medical University Cancer Hospital, Nanning, China.
Jie ZhaoDepartment of Medical Records, Guangxi Medical University Cancer Hospital, Nanning, China.
Huiliu ZhaoDepartment of Clinical Laboratory, Guangxi Medical University Cancer Hospital, Nanning, China.
Fengfei LiuDepartment of Clinical Laboratory, Guangxi Medical University Cancer Hospital, Nanning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: nuclear-associated antigen Ki67 (Ki67) emerges as a clinically practical biomarker for proliferation assessment among many cancer types. However, the definite prognostic value of Ki67 against a specific cancer type has remained vague. This study aims to perform a comprehensive pan-cancer analysis of the prognosis value of Ki67 across various cancer types. Methods: This study explored the expression, prognostic value, and tumor-infiltrating immune of MKI67 in the TCGA database by pan-cancer, and then performed immunohistochemical, correlation analysis and prognostic analysis using 10028 patients of the top 10 cancer patients in China we collected. The correlation between MKI67 expression and survival outcome, clinical features, MSI, TMB, and tumor-infiltrating immune cells by TCGA database, xCell, and TIMER algorithms. Results: MKI67 expression was significantly upregulated across varied cancer types verified by datasets. We found MKI67 expression was significantly associated with poor prognosis in LUADLUSC, LIHC, and BRCA patients, but good prognosis in COADREAD and READ patients via Kaplan-Meier survival analysis using 10028 patients collected. These results of our validation were generally consistent with TCGA database except BRCA, COADREAD and READ. Meanwhile, upregulation of MKI67 elevates the degree of immune infiltration of several immune cell subtypes, such as functional T cells, CD4 Conclusion: Our comprehensive analysis may supply useful guidance on MKI67 applicability across various cancer types. These observed results contribute to the promise of MKI67 in a realistic clinical setting and improve the outcomes of cancer patients.

Indexed as

Biomarkers, TumorKi-67 AntigenNeoplasmsFemaleGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateLymphocytes, Tumor-InfiltratingMalePrognosisTumor MicroenvironmentBiomarkers, TumorKi-67 AntigenMKI67 protein, humancancer immunityMKI67multi-omics bioinformaticspathwayprognosis

Identifiers

PMID40070823
PMCPMC11894575

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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.