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一种与PD-L1和肿瘤突变负荷相关的联合双信使核糖核酸特征用于肺腺癌预后评估

A Combined Two-mRNA Signature Associated With PD-L1 and Tumor Mutational Burden for Prognosis of Lung Adenocarcinoma.

作者信息

Song Congkuan, Wu Zhiquan, Wang Qingwen, Wang Yujin, Guo Zixin, Li Sheng, Hu Weidong

机构信息

Department of Thoracic Surgery, Zhongnan Hospital of Wuhan University, Wuhan, China.

Hubei Key Laboratory of Tumor Biological Behaviors and Hubei Cancer Clinical Study Center, Wuhan, China.

出版信息

Front Cell Dev Biol. 2021 Jan 26;9:634697. doi: 10.3389/fcell.2021.634697. eCollection 2021.

Abstract

Due to biological heterogeneity, lung adenocarcinoma (LUAD) patients with the same stage may exhibit variable responses to immunotherapy and a wide range of outcomes. It is urgent to seek a biomarker that can predict the prognosis and response to immunotherapy in these patients. In this study, we identified two genes (ANLN and ARNTL2) from multiple gene expression data sets, and developed a two-mRNA-based signature that can effectively distinguish high- and low-risk patients and predict patients' response to immunotherapy. Furthermore, taking full advantage of the complementary value of clinical and molecular features, we combined the immune prognostic signature with clinical features to construct and validate a nomogram that can predict the probability of high tumor mutational burden (>10 mutations per megabyte). This may improve the estimation of immunotherapy response in LUAD patients, and provide a new perspective for clinical screening of immunotherapy beneficiaries.

摘要

由于生物异质性,相同分期的肺腺癌(LUAD)患者对免疫疗法可能表现出不同的反应和广泛的预后情况。迫切需要寻找一种能够预测这些患者预后和免疫疗法反应的生物标志物。在本研究中,我们从多个基因表达数据集中鉴定出两个基因(ANLN和ARNTL2),并开发了一种基于两个mRNA的特征,可有效区分高风险和低风险患者,并预测患者对免疫疗法的反应。此外,充分利用临床和分子特征的互补价值,我们将免疫预后特征与临床特征相结合,构建并验证了一种列线图,该列线图可预测高肿瘤突变负担(每兆碱基>10个突变)的概率。这可能会改善对LUAD患者免疫疗法反应的评估,并为临床筛选免疫疗法受益患者提供新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d73d/7875126/a834d094acb8/fcell-09-634697-g001.jpg

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