Wang Luan, Chen Xinyu, Yu Hanzhong, Wang Guannan, Han Dong
Department of Cardiothoracic Surgery, The Affiliated Xuzhou Municipal Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.
Department of Clinical Laboratory, The Affiliated Xuzhou Municipal Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.
Cell Biochem Biophys. 2025 Jul 14. doi: 10.1007/s12013-025-01805-3.
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.
铜死亡是一种最近被确定的由铜离子驱动的程序性细胞死亡形式,与癌症进展有关,但其在肺腺癌(LUAD)中的预后意义仍不清楚。在本研究中,我们使用多个公共数据集探索了19个铜死亡相关基因(CuRGs)的表达模式和预后相关性。共识聚类分析将LUAD患者分为两种不同的分子亚型,其临床结局和免疫特征存在显著差异。鉴定了两种亚型之间的差异表达基因(DEGs),功能富集分析揭示了与免疫途径的显著关联线索。使用LASSO-Cox回归构建了一个包含五个基因的预后风险特征(CuRG_score),并在三个独立的GEO数据集中进行了验证。CuRG_score有效地将患者分为高风险和低风险组,总生存率存在显著差异义。各数据集中的AUC值分别为0.761、0.618和0.642,显示出强大的预测能力。进一步分析表明,高风险患者表现出免疫抑制特征,包括CD8+T细胞和NK细胞浸润较低。此外,免疫检查点表达和免疫表型评分(IPS)分析表明,低风险患者可能从免疫治疗中获益更多。总之,我们的研究确定了一种基于CuRG的新型分子特征,可作为LUAD预后的有力预测指标,并为个性化免疫治疗策略提供潜在指导。