ArticleDiscover oncology2025
Comprehensive analysis of zinc finger protein 367 as a potential pan-cancer diagnostic and prognostic biomarker and underlying biological mechanisms.
Article in Discover 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.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveZinc finger protein 367 (ZNF367) acts as a transcription factor and has been identified as overexpressed in numerous cancers. However, the clinical significance of ZNF367 in various cancers remains fragmentary. Therefore, this study performs a comprehensive pan-cancer analysis of ZNF367 for its diagnostic and prognostic value and underlying biological mechanisms across multiple cancer types.
methodsMulti-omics data from the website databases were utilized for analyzing the pan-cancer expression landscape of ZNF367 and its potential diagnostic and prognostic significance, and validating its expression in some cancers by immunohistochemistry, followed by a series of biological analyses using online bioinformatics tools to investigate the underlying mechanisms, including the genetic and epigenetic alterations of the ZNF367 gene, interaction networks of ZNF367 with proteins and genes, associations of ZNF367 with tumor genetic heterogeneity and tumor microenvironment characteristics.
resultsZNF367 expression levels were elevated in the majority of cancers, validated its overexpression of protein in some cancers, and showed moderate to high diagnostic performance in 26 cancer types. Overexpression of ZNF367 was connected with unfavorable prognostic outcomes across several malignancies and acted as an independent risk factor using multivariate Cox regression analysis in some tumors. Common genetic alterations of ZNF367 included mutations and amplifications. KEGG functional analysis uncovered that ZNF367-associated genes participated in multiple cancer-related pathways. Significant correlations were observed between ZNF367 and tumor genetic heterogeneity, DNA methylation, immune infiltration and ZNF367-related genes in most cancers.
conclusionZNF367 may emerge as a valuable pan-cancer diagnostic and prognostic biomarker supported by biological evidence.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.