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一种用于老年肺腺癌患者风险分层、预后预测以及化疗和免疫治疗获益评估的由七个衰老相关基因组成的新型特征。

A novel signature of seven aging-related genes for risk stratification, prognosis prediction and benefit evaluation of chemotherapy, and immunotherapy in elderly patients with lung adenocarcinoma.

作者信息

Tian Yi, Zhao Wenya, Lin Chenjing, Chen Yang, Lin Qiaoxin, Liu Yiru, Gu Dianna, Tian Ling

机构信息

Department of Central Laboratory, Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200030, China.

Department of Medical Oncology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, China.

出版信息

Heliyon. 2024 Jun 18;10(12):e33268. doi: 10.1016/j.heliyon.2024.e33268. eCollection 2024 Jun 30.

Abstract

BACKGROUND

Aging, a multifaceted biological process, is thought to be associated with lung adenocarcinoma (LUAD) development and progression. However, it is unclear whether aging-related genes (ARGs) can predict tumor risk, chemotherapy and immunotherapy benefits, and prognosis in LUAD patients at different ages.

METHODS

Gene expression datasets and clinical information of LUAD patients were downloaded from TCGA and GEO database. Univariate and multivariate Cox regression, and lasso algorithm were employed to identify the ARG signatures. Patients were stratified into high-risk and low-risk groups to evaluate the predictive accuracy using Kaplan-Meier curves, ROC curves, and time-dependent AUC. A nomogram was established to predict the survival probability. GSEA revealed potential pathways, and CIBERSORT indicated different immunologic status. TIDE score was used to predict the potential tumor response to immune checkpoint inhibitors, and GDSC was employed to evaluate the sensitivity of chemotherapeutic drugs. The correlation of TIDE score and patient age, as well as that of ARGs and patient age was investigated. And cell Culture and RT-qPCR for external validation for key gene.

RESULTS

A novel gene signature based on seven ARGs was established, including BMP15, CD79A, CDKN3, CDX2, COL1A1, DKK1, and GRIK2. Our model demonstrated exceptional prediction accuracy for elderly LUAD patients of 71-90 years old. A nomogram model was constructed to predict the survival probability, and the C-index value was 0.737, indicating our prognostic nomogram model has high accuracy. Through external RT-qPCR validation, we found that CD79A expression in H1299 was higher than that of BEAS-2B. And novel immunotherapy and chemotherapy regimens were accordingly proposed for the elderly LUAD patients.

CONCLUSION

We identified a novel gene signature based on seven ARGs for risk stratification, prognosis prediction and benefit evaluation of immunotherapy and chemotherapy in elderly LUAD patients.

摘要

背景

衰老作为一个多方面的生物学过程,被认为与肺腺癌(LUAD)的发生发展相关。然而,尚不清楚衰老相关基因(ARGs)能否预测不同年龄段LUAD患者的肿瘤风险、化疗及免疫治疗获益情况和预后。

方法

从TCGA和GEO数据库下载LUAD患者的基因表达数据集和临床信息。采用单因素和多因素Cox回归以及套索算法来识别ARGs特征。将患者分为高风险和低风险组,使用Kaplan-Meier曲线、ROC曲线和时间依赖性AUC评估预测准确性。建立列线图以预测生存概率。基因集富集分析(GSEA)揭示潜在通路,CIBERSORT表明不同的免疫状态。TIDE评分用于预测肿瘤对免疫检查点抑制剂的潜在反应,利用基因表达综合数据库(GDSC)评估化疗药物的敏感性。研究TIDE评分与患者年龄的相关性以及ARGs与患者年龄的相关性。并进行细胞培养和RT-qPCR对关键基因进行外部验证。

结果

基于7个ARGs建立了一种新的基因特征,包括骨形态发生蛋白15(BMP15)、CD79A、细胞周期蛋白依赖性激酶3(CDKN3)、尾型同源盒转录因子2(CDX2)、Ⅰ型胶原α1链(COL1A1)、 Dickkopf相关蛋白1(DKK1)和谷氨酸离子型受体钾离子通道亚基2(GRIK2)。我们的模型对71-90岁的老年LUAD患者显示出卓越的预测准确性。构建了一个列线图模型来预测生存概率,C指数值为0.737,表明我们的预后列线图模型具有较高的准确性。通过外部RT-qPCR验证,我们发现H1299中CD79A的表达高于BEAS-2B。并据此为老年LUAD患者提出了新的免疫治疗和化疗方案。

结论

我们基于7个ARGs鉴定了一种新的基因特征,用于老年LUAD患者的风险分层、预后预测以及免疫治疗和化疗的获益评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbb5/11252982/5fa65ab30b30/gr1.jpg

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