Evidence map›Paper›PMID 40658149›Full record

ArticleCell biochemistry and biophysics2025

Identification Cuproptosis-related Genes Signature to Predict the Prognosis of Lung Cancer.

Luan Wang, Xinyu Chen, Hanzhong Yu, Guannan Wang, Dong Han

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Article in Cell biochemistry and biophysics, 2025. 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Luan WangDepartment of Cardiothoracic Surgery, The Affiliated Xuzhou Municipal Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.
Xinyu ChenDepartment of Cardiothoracic Surgery, The Affiliated Xuzhou Municipal Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.
Hanzhong YuDepartment of Clinical Laboratory, The Affiliated Xuzhou Municipal Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.
Guannan WangDepartment of Pharmaceutical, The Affiliated Xuzhou Municipal Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China. 17712982016@163.com.
Dong HanDepartment of Cardiothoracic Surgery, The Affiliated Xuzhou Municipal Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China. xzsdyrmyyxwk@163.com.

Funding

2021 Xuzhou Municipal Health Commission Youth Medical Science and Technology Innovation Project XWKYSL20210147
6 · The paper itself

Abstract

Cuproptosis, a recently characterized form of regulated cell death driven by copper ions, has been implicated in cancer progression, yet its prognostic significance in lung adenocarcinoma (LUAD) remains unclear. In this study, we explored the expression patterns and prognostic relevance of 19 cuproptosis-related genes (CuRGs) using multiple public datasets. Consensus clustering analysis stratified LUAD patients into two distinct molecular subtypes with significant differences in clinical outcomes and immune characteristics. Differentially expressed genes (DEGs) between the two subtypes were identified, and functional enrichment analysis revealed significant associations with immune pathways. A prognostic risk signature (CuRG_score) comprising five genes was constructed using LASSO-Cox regression and validated across three independent GEO datasets. The CuRG_score effectively stratified patients into high- and low-risk groups with significant differences in overall survival. The AUC values were 0.761, 0.618, and 0.642 across the datasets, respectively, demonstrating strong predictive power. Further analysis revealed that high-risk patients exhibited immunosuppressive features, including lower infiltration of CD8+T cells and NK cells. Moreover, immune checkpoint expression and immunophenoscore (IPS) analysis suggested that low-risk patients may benefit more from immunotherapy. In conclusion, our study identifies a novel CuRG-based molecular signature that serves as a robust predictor of LUAD prognosis and offers potential guidance for personalized immunotherapy strategies.

Indexed as

Adenocarcinoma of LungCopperLung NeoplasmsDatabases, GeneticGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMalePrognosisTranscriptomeCopperCuproptosisImmune cell infiltrationLung cancerMolecular subtypesPrognosis

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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.