Evidence map›Paper›PMID 42737631›Full record

ArticleInternational journal of molecular sciences2026

Comprehensive Analysis of Cuproptosis-Related Genes According to Cancer Stage and Their Prognostic Value in Cervical Cancer.

Jing He, Yueyan Sun, Zhonghua Yang, Duo Xu, Pengxia Zhang, Jiaqi Xia

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Article in International journal of molecular sciences, 2026. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

6 authors.

Jing HeSchool of Basic Medical Sciences, Jiamusi University, Jiamusi 154007, China.
Yueyan SunSchool of Clinical Medical Sciences, Jiamusi University, Jiamusi 154007, China.
Zhonghua YangSchool of Basic Medical Sciences, Jiamusi University, Jiamusi 154007, China.
Duo XuSchool of Clinical Medical Sciences, Jiamusi University, Jiamusi 154007, China.ORCID 0009-0008-7231-1605
Pengxia ZhangSchool of Basic Medical Sciences, Jiamusi University, Jiamusi 154007, China.
Jiaqi XiaSchool of Basic Medical Sciences, Jiamusi University, Jiamusi 154007, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cuproptosis is a novel form of metabolism-associated cell death. Cervical cancer (CC) exhibits elevated serum copper levels and mitochondrial metabolic reprogramming, making cuproptosis-related genes (CRGs) potentially critical for prognosis prediction and therapeutic targeting. However, studies on CRGs in CC remain limited. This study aimed to construct prognostic and cancer staging models for CC using machine learning (ML) algorithms. Gene expression profiles of patients with CC were obtained from the TCGA and GEO databases. Five ML algorithms were employed to identify significant factors, including random forest (RF), support vector machine (SVM), Gaussian mixture model (GMM), Bayesian, and StepCox. A prognostic model was subsequently constructed using LASSO-Cox regression based on the selected genes. Concurrently, a cancer staging model was built using ML algorithms incorporating three distinct gene categories. Finally, qRT-PCR and Western blotting were conducted to validate the expression of signature genes at both the tissue and cellular levels. Additionally, CTD-based screening and in vitro functional assays were performed to evaluate the effects of DDP on CC cells. Through integrated bioinformatics and ML approaches, a prognostic model comprising nine CRGs was successfully established (GMM = 0.72). The derived risk score served as an independent prognostic indicator for CC (

Indexed as

Biomarkers, TumorCuproptosisUterine Cervical NeoplasmsFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMachine LearningNeoplasm StagingPrognosisBiomarkers, Tumorcancer staging modelcervical cancercuproptosis-related genesmachine learning algorithmprognostic model

Identifiers

PMID42737631
PMCPMC13566246

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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.