Evidence map›Paper›PMID 42832574›Full record

ArticlePloS one2026

Exploring the key genes of colorectal "adenoma-cancer" based on graph transformer.

Yue Yuan, Yu Liu, Jingchun Fan, Zhen Ren

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Yue YuanSchool of Information Engineering, Gansu University of Chinese Medicine, Lanzhou, China.ORCID https://orcid.org/0009-0006-6808-8688
Yu LiuSchool of Information Engineering, Gansu University of Chinese Medicine, Lanzhou, China.
Jingchun FanCenter for Evidence-based Medicine, Gansu University of Chinese Medicine, Lanzhou, China.
Zhen RenSchool of Information Engineering, Gansu University of Chinese Medicine, Lanzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is one of the most lethal malignancies worldwide, and the precise identification of biomarkers from colonic adenoma to cancer is of great significance for preventing the development of adenocarcinoma. Given that existing methods inadequately capture the topological network relationships among genes, this study proposes a graph neural network model based on multifeature learning, named ChebTs, to investigate the correlation between key genes involved in the colorectal "adenoma-cancer" transition. The GSE41657 and GSE31905 datasets from the GEO database were stratified into normal, adenoma, and colorectal cancer groups. Feature encoding was introduced to enhance node features, followed by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses of differentially expressed genes (DEGs). A protein-protein interaction (PPI) network was constructed using Cytoscape software, and the aggregated information was embedded into the model for training to generate a list of key genes with corresponding importance scores. An attention pooling mechanism aggregated node-level representations into graph level representations for sample classification, and a two layer fully connected network, following activation and regularization, produced predicted probabilities. Furthermore, we provided interpretable analyses at the gene level using GNNExplainer. The results were validated through virtual knockout techniques. The eight screened genes, Fibronectin 1 (FN1), Claudin 2 (CLDN2), Interleukin-33 (IL-33), Matrix Metallopeptidase 1 (MMP1), Stanniocalcin 2 (STC2), Insulin-Like Growth Factor-Binding Protein 7 (IGFBP7), NADPH Oxidase 4 (NOX4), and Secreted Frizzled Related Protein 1 (SFRP1), were all found to be associated with overall survival (OS) in CRC. In this study, eight molecules closely related to the development of colorectal adenocarcinoma were screened out, and they may be diagnostic biomarkers of colorectal cancer. These genes affect the prognosis of patients by participating in biological processes such as remodeling of extracellular mechanisms, and are of great significance for preventing the carcinogenesis of adenoma.

Indexed as

AdenomaColorectal NeoplasmsBiomarkers, TumorDatabases, GeneticGene Expression ProfilingGene Expression Regulation, NeoplasticGene Regulatory NetworksGraph Neural NetworksHumansProtein Interaction MapsBiomarkers, Tumor

Identifiers

PMID42832574
PMCPMC13638036

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.