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铜诱导的细胞死亡相关长链非编码RNA在肺鳞状细胞癌中的预后及治疗潜力

Prognostic and therapeutic potential of copper-induced cell death-related lncRNAs in lung squamous cell carcinoma.

作者信息

Tian Zhe, Cen Lilan, Hua Haoming, Wei Feng, Dong Jue, Huang Yulan, Wang Zhibo, Deng Junhua, Jiang Yujie

机构信息

Department of Pulmonary and Critical Care Medicine, Affiliated Hospital of Youjiang Medical University for Nationalities, No. 18, Zhongshan 2 Road, Youjiang District, Baise, 533000, Guangxi, China.

Life Science and Clinical Medicine Research Center, Affiliated Hospital of Youjiang Medical University for Nationalities, No. 18, Zhongshan 2 Road, Youjiang District, Baise, 533000, Guangxi, China.

出版信息

Clin Exp Med. 2025 May 3;25(1):135. doi: 10.1007/s10238-025-01663-6.

DOI:10.1007/s10238-025-01663-6
PMID:40316808
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12048434/
Abstract

Lung squamous cell carcinoma (LUSC), a major subtype of non-small cell lung cancer, remains challenging to treat due to poor prognosis and limited therapeutic options. This study investigates the prognostic and therapeutic implications of copper-induced cell death-related long non-coding RNAs (lncRNAs) in LUSC using data from The Cancer Genome Atlas. Five lncRNAs (AC010328.1, LINC01740, AL358613.2, MIR3945HG, AC002467.1) were identified as independent prognostic markers and incorporated into a risk score model to stratify patients into high- and low-risk groups. Survival analyses revealed significant differences in overall survival, with the high-risk group exhibiting higher immune evasion potential and poorer response to immunotherapy. Functional enrichment analyses highlighted the involvement of these lncRNAs in drug metabolism and tumor biology. Furthermore, tumor mutation burden analysis and immune dysfunction evaluation confirmed the clinical relevance of the model, identifying high-risk patients as more sensitive to targeted drugs such as Quizartinib and Dasatinib. A Nomogram integrating lncRNA risk scores and clinical factors demonstrated robust predictive accuracy for 1-, 3-, and 5-year survival outcomes. This study provides novel biomarkers and actionable insights for improving prognostic assessment and personalizing immunotherapy strategies for LUSC patients.

摘要

肺鳞状细胞癌(LUSC)是非小细胞肺癌的一种主要亚型,由于预后不良和治疗选择有限,其治疗仍然具有挑战性。本研究利用癌症基因组图谱(The Cancer Genome Atlas)的数据,调查了铜诱导的细胞死亡相关长链非编码RNA(lncRNA)在LUSC中的预后和治疗意义。鉴定出5种lncRNA(AC010328.1、LINC01740、AL358613.2、MIR3945HG、AC002467.1)作为独立的预后标志物,并将其纳入风险评分模型,将患者分为高风险组和低风险组。生存分析显示总生存期存在显著差异,高风险组表现出更高的免疫逃逸潜力,对免疫治疗的反应更差。功能富集分析强调了这些lncRNA在药物代谢和肿瘤生物学中的作用。此外,肿瘤突变负荷分析和免疫功能障碍评估证实了该模型的临床相关性,确定高风险患者对如奎扎替尼和达沙替尼等靶向药物更敏感。整合lncRNA风险评分和临床因素的列线图对1年、3年和5年生存结局显示出强大的预测准确性。本研究为改善LUSC患者的预后评估和个性化免疫治疗策略提供了新的生物标志物和可行的见解。

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