Evidence map›Paper›PMID 40636694›Full record

ArticleFrontiers in oncology2025

Multidimensional analysis suggests that ZNF433 is a promising biomarker for the diagnosis and prognosis of human cancers.

Lingyu Xie, Xin Zeng, Hui Luo, Bin Xie, Xuefeng Wang, Nan Wu, Junrong Zou, Guoxi Zhang, Xiaofeng Zou, Hui Xu

Abstract read
In one paragraph

Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Lingyu XieThe First Clinical College, Gannan Medical University, Ganzhou, Jiangxi, China.
Xin ZengThe First Clinical College, Gannan Medical University, Ganzhou, Jiangxi, China.
Hui LuoThe First Clinical College, Gannan Medical University, Ganzhou, Jiangxi, China.
Bin XieDepartment of Urology, Shanggao County People's Hospital, Yichun, China.
Xuefeng WangDepartment of Surgery, Changshan County People's Hospital, Quzhou, China.
Nan WuThe First Clinical College, Gannan Medical University, Ganzhou, Jiangxi, China.
Junrong ZouDepartment of Urology, The First Affiliated Hospital of Gannan Medical University, Ganzhou, Jiangxi, China.
Guoxi ZhangDepartment of Urology, The First Affiliated Hospital of Gannan Medical University, Ganzhou, Jiangxi, China.
Xiaofeng ZouDepartment of Urology, The First Affiliated Hospital of Gannan Medical University, Ganzhou, Jiangxi, China.
Hui XuDepartment of Urology, The First Affiliated Hospital of Gannan Medical University, Ganzhou, Jiangxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Zinc finger proteins, particularly members of the Krüppel-associated box zinc finger proteins (KRAB-ZFPs), play critical roles in regulating gene expression, cell cycle progression, and epigenetic modifications. Despite the growing body of research on KRAB-ZFPs, the role of ZNF433, a relatively less studied member of this family, remains poorly understood in the context of cancer. Methods: We conducted multi-dimensional analyses using publicly available databases, including TCGA and GTEx, to evaluate ZNF433's expression patterns, genetic mutations, survival outcomes, immune microenvironment interactions, and diagnostic potential across different cancers. Functional enrichment and protein interaction network analyses were also performed to explore its potential involvement in cancer-related pathways. Results: Our findings revealed that ZNF433 is significantly downregulated in most cancer types, with stage-dependent expression patterns observed in KIRC and KIRP. High expression of ZNF433 was associated with improved overall survival (OS) in HNSC and KIRC, while in ESCA and PRAD, it was correlated with poorer disease-free survival (DFS). Additionally, high ZNF433 levels were linked to better DFS in BRCA, KIRP, THYM, and KIRC. ZNF433 expression was also closely associated with genomic instability markers, including tumor mutational burden (TMB), microsatellite instability (MSI), and mismatch repair (MMR) deficiencies. Furthermore, ZNF433 exhibited significant regulatory roles within the tumor immune microenvironment. Diagnostic analysis showed that ZNF433 has strong diagnostic potential in LAML and TGCT, and moderate diagnostic value in other cancers. Conclusions: Our study highlights the potential of ZNF433 as a diagnostic and prognostic biomarker and provides new insights into its potential as a therapeutic target.

Indexed as

bioinformaticsbiomarkersdiagnosisprognosisZNF433

Identifiers

PMID40636694
PMCPMC12237650

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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.