Chen Feihong, Wen Xin, Wu Jiani, Feng Min, Feng Shicheng
Pharmaceutical Research Center, School of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189, China.
Department of Radiotherapy, Zhongda Hospital, Southeast University, Nanjing 210009, China.
Pharmaceuticals (Basel). 2024 Sep 21;17(9):1244. doi: 10.3390/ph17091244.
As a novel discovered mechanism of cell death, cuproptosis is copper-dependent and induces protein toxicity related to advanced tumors, disease prognosis, and human innate and adaptive immune response. However, it has not yet been fully established how the prognosis of lung adenocarcinoma (LUAD) is related to the immune microenvironment of cuproptosis-related lncRNAs using several bioinformatic techniques. In the study, 19 genes related to cuproptosis were collected. Subsequently, 783 lncRNAs related to the co-expression of cuproptosis were obtained. Moreover, the Cox model revealed and constructed four lncRNA (, , , ) prognostic markers related to cuproptosis. Based on the median risk score (RS) values, patients were categorized into two groups: high risk and low risk. The Kaplan-Meier (KM) survival curve depicted a statistically significant overall survival (OS) rate among two groups. Principal component analysis (PCA) and receiver operator characteristic curve (ROC) proved that the model had promising ability in prognosis. The analysis of univariate and multivariate Cox regression revealed that RS served as an independent prognostic factor. Moreover, multivariate Cox regression was employed for the establishment of a nomogram of prognostic indicators. The tumor mutational burden (TMB) depicted a considerable difference between the two risk groups. The immunotherapy response of LUAD patients with high risk was improved compared to low risk patients. The study also revealed that drug sensitivity associated with LUAD was significantly linked to RS. The findings could be helpful to establish a good diagnosis, prognosis, and management regime for patients with LUAD.
作为一种新发现的细胞死亡机制,铜死亡是铜依赖性的,并诱导与晚期肿瘤、疾病预后以及人类固有和适应性免疫反应相关的蛋白质毒性。然而,尚未完全明确如何使用多种生物信息学技术,将肺腺癌(LUAD)的预后与铜死亡相关lncRNA的免疫微环境联系起来。在该研究中,收集了19个与铜死亡相关的基因。随后,获得了783个与铜死亡共表达相关的lncRNA。此外,Cox模型揭示并构建了四个与铜死亡相关的lncRNA(,,,)预后标志物。根据中位风险评分(RS)值,将患者分为两组:高风险组和低风险组。Kaplan-Meier(KM)生存曲线显示两组之间的总生存率(OS)具有统计学意义。主成分分析(PCA)和受试者工作特征曲线(ROC)证明该模型在预后方面具有良好的能力。单变量和多变量Cox回归分析表明,RS是一个独立的预后因素。此外,采用多变量Cox回归建立了预后指标列线图。肿瘤突变负担(TMB)在两个风险组之间存在显著差异。与低风险患者相比,高风险LUAD患者的免疫治疗反应有所改善。该研究还表明,与LUAD相关的药物敏感性与RS显著相关。这些发现可能有助于为LUAD患者建立良好的诊断、预后和管理方案。