Evidence map›Paper›PMID 42397623›Full record

ArticleDiscover oncology2026

Comprehensive identification of three key genes and three key DNA methylation CpG sites associated with prognosis and prediction in colon adenocarcinoma.

Yu-Xian Liu, Xingjie Chen, Wenjia Wang, Junyuan Zhang, Ziyi Wang, Hao Lin, Yan-Ni Cao

Abstract read
In one paragraph

Article in Discover oncology, 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
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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

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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

7 authors.

Yu-Xian LiuSchool of Artificial Intelligence, Anhui University of Science and Technology, No.168 Taifeng Street, Tianjia'an District, Huainan, 232001, People's Republic of China.
Xingjie ChenSchool of Artificial Intelligence, Anhui University of Science and Technology, No.168 Taifeng Street, Tianjia'an District, Huainan, 232001, People's Republic of China.
Wenjia WangSchool of Artificial Intelligence, Anhui University of Science and Technology, No.168 Taifeng Street, Tianjia'an District, Huainan, 232001, People's Republic of China.
Junyuan ZhangSchool of Artificial Intelligence, Anhui University of Science and Technology, No.168 Taifeng Street, Tianjia'an District, Huainan, 232001, People's Republic of China.
Ziyi WangSchool of Artificial Intelligence, Anhui University of Science and Technology, No.168 Taifeng Street, Tianjia'an District, Huainan, 232001, People's Republic of China.
Hao LinKey Laboratory for Neuro-Information of Ministry of Education, Center for Informational Biology, School of Life Sciences and Technology, University of Electronic Science and Technology of China, Chengdu, 611731, People's Republic of China. hlin@uestc.edu.cn.
Yan-Ni CaoSchool of Artificial Intelligence, Anhui University of Science and Technology, No.168 Taifeng Street, Tianjia'an District, Huainan, 232001, People's Republic of China. cyn@aust.edu.cn.ORCID https://orcid.org/0000-0003-1508-4131

Funding

the National Natural Science Foundation of China 62501014the National Natural Science Foundation of China 62502005the Natural Science Research Project of Anhui Educational Committee 2023AH051200the Natural Science Research Project of Anhui Educational Committee 2023AH051201
6 · The paper itself

Abstract

Colon adenocarcinoma (COAD) is a common cancer with high incidence and mortality rates worldwide. DNA methylation has a significant impact on the occurrence and development of COAD. However, the regulatory and prognostic effects of DNA methylation in different regions on COAD remain unclear. This study analyzed the methylation of 12 different regions in COAD and normal colon tissue, revealing the differences in methylation distribution and the stability of methylation levels in COAD. Then, correlation analysis of differentially expressed genes and differentially methylated sites in different regions shows that methylation has an inhibitory effect on gene expression. Next, we performed Cox regression analysis and survival analysis based on clinical data, and identified three key genes (GSTM1, POU3F3, and RNF32) related to survival. We also constructed a prognostic risk scoring model, which demonstrated good predictive performance for prognosis. Furthermore, we identified three key DNA methylation CpG sites and their regulatory regions in three key genes. Subsequently, we constructed 120 COAD prediction models using 10 machine learning algorithms. The results show that these key genes and key DNA methylation CpG sites have very good predictive performance for COAD. Finally, we analyzed the immune microenvironment of three key genes and identified potential drugs associated with them. These results may provide theoretical support for the study of the regulatory mechanism of DNA methylation on gene expression, and may also provide potential biomarkers for the prognosis and early diagnosis of COAD.

Indexed as

BiomarkersColon adenocarcinomaDNA methylationGene expressionMachine learningPrognosis

Identifiers

PMID42397623
PMCPMC13388623

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

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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 Socratic graph.