Evidence map›Paper›PMID 40463372›Full record

ArticleFrontiers in immunology2025

Construction of a prognostic model for endometrial cancer related to programmed cell death using WGCNA and machine learning algorithms.

Weicheng Pan, Jinlian Cheng, Shanshan Lin, Qianxi Li, Yuanyuan Liang, Huiying Li, Xianxian Nong, Huizhen Nong

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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

8 authors.

Weicheng PanDepartment of Obstetrics and Gynecology, Wuming Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Jinlian ChengDepartment of Obstetrics and Gynecology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Shanshan LinDepartment of Obstetrics and Gynecology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Qianxi LiDepartment of Obstetrics and Gynecology, Wuming Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Yuanyuan LiangDepartment of Obstetrics and Gynecology, Wuming Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Huiying LiDepartment of Obstetrics and Gynecology, Wuming Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Xianxian NongDepartment of Obstetrics and Gynecology, Wuming Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Huizhen NongDepartment of Obstetrics and Gynecology, Wuming Hospital of Guangxi Medical University, Nanning, Guangxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Programmed cell death (PCD) refers to a regulated and active process of cellular demise, initiated by specific biological signals. PCD plays a crucial role in the development, progression, and drug resistance of uterine corpus endometrial carcinoma (UCEC), making the exploration of its relationship with UCEC prognosis highly clinically relevant. Methods: Data from UCEC patients and control cohorts were obtained from The Cancer Genome Atlas (TCGA) database. Differentially expressed genes (DEGs) were identified and subsequently intersected with a PCD gene set to discern PCD-related differentially expressed genes (PCD-DEGs). To isolate core prognostic PCD-DEGs, methods including consistency clustering analysis, weighted gene co-expression network analysis (WGCNA), univariate Cox regression analysis, and five machine learning techniques for dimensionality reduction were utilized. Validation of three core prognostic PCD-DEGs was conducted using RT-qPCR, and these genes were used to develop a prognostic model. Additionally, an analysis of drug sensitivity was performed. Results: Consistency clustering analysis revealed significant differences in prognosis and tumor microenvironment among subtypes, strongly associated with various immune subtypes. The three core prognostic PCD-DEGs identified-SRPX, NT5E, and ATP6V1C2-were instrumental in constructing the lasso prognostic model and nomogram. Receiver Operating Characteristic (ROC) curve analysis confirmed the model's strong prognostic performance and clinical applicability. The high-risk group exhibited lower tumor mutation frequencies, a higher propensity for immune escape, reduced response to immune therapy, and potential benefits from potent chemotherapy drugs. Conclusion: This study developed a prognostic model related to PCD for UCEC using comprehensive bioinformatics analyses. The model demonstrates robust predictive performance and holds significant potential for clinical application, thereby facilitating precise stratification and personalized treatment of UCEC patients.

Indexed as

ApoptosisBiomarkers, TumorEndometrial NeoplasmsGene Regulatory NetworksMachine LearningComputational BiologyDatabases, GeneticFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansPrognosisTumor MicroenvironmentBiomarkers, Tumorendometrial cancermachine learningprognostic modelprogrammed cell deathWGCNA

Identifiers

PMID40463372
PMCPMC12129963

What Socratic holds

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LicenceCC BY
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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.