Identification of Stem Cell-related Gene Markers by Comprehensive Transcriptome Analysis to Predict the Prognosis and Immunotherapy of Lung Adenocarcinoma.

IF 2.1 4区 医学 Q4 CELL & TISSUE ENGINEERING
Hongzhang Lai, Xiwu Wen, Yukun Peng, Long Zhang
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引用次数: 0

Abstract

Background: Cancer stem cells (CSCs) contribute to metastasis and drug resistance to immunotherapy in lung adenocarcinoma (LUAD), so the stemness evaluation of cancer cells is of great significance.

Method: The single-cell RNA sequencing (scRNA-seq) data of the GSE149655 dataset were collected and analyzed. Malignant cells were distinguished by CopyKAT. CytoTRACE score of marker genes in malignant cells was counted by CytoTRACE to construct the stemness score formula. Sample stemness score in TCGA was determined by the formula and divided into high-, medium- and low-stemness score groups. LASSO and COX regression analyses were carried out to screen the key genes related to the prognosis of LUAD from the differentially expressed genes (DEGs) in high- and low-stemness score groups and a risk score model was constructed.

Result: Seven types of cells were identified from a total of 4 samples, and 193 marker genes of 3455 malignant cells were identified. There were 1098 DEGs between low- and high-stemness score groups of TCGA, of which CPS1, CENPK, GJB3, and TPSB2 constituted gene signatures. The 4-gene signature could independently evaluate LUAD survival in the training and validation sets and showed an acceptable area under the receiver operator characteristic (ROC) curves (AUCs).

Conclusion: This study provides insights into the cellular heterogeneity of LUAD and develops a new cancer stemness evaluation indicator and a 4-gene signature as a potential tool for evaluating the response of LUAD to immune checkpoint blockade (ICB) therapy or antineoplastic therapy.

通过综合转录组分析鉴定干细胞相关基因标记以预测肺腺癌的预后和免疫疗法
背景:癌症干细胞(CSCs)会导致肺腺癌(LUAD)的转移和免疫治疗的耐药性,因此对癌细胞的干性进行评估具有重要意义:方法:收集并分析GSE149655数据集中的单细胞RNA测序(scRNA-seq)数据。方法:收集 GSE149655 数据集的单细胞 RNA 测序(scRNA-seq)数据并进行分析。通过CytoTRACE计算恶性细胞中标记基因的CytoTRACE得分,从而构建干性得分公式。根据公式确定 TCGA 中样本的干性得分,并将其分为高、中、低干性得分组。通过LASSO和COX回归分析,从高干度组和低干度组的差异表达基因(DEGs)中筛选出与LUAD预后相关的关键基因,并构建风险评分模型:结果:共从4个样本中鉴定出7种类型的细胞,并从3455个恶性细胞中鉴定出193个标记基因。在 TCGA 的低干度量组和高干度量组之间有 1098 个 DEGs,其中 CPS1、CENPK、GJB3 和 TPSB2 构成了基因特征。在训练集和验证集中,4个基因特征能独立评估LUAD的存活率,并显示出可接受的接收者操作者特征曲线(ROC)下面积(AUC):本研究深入揭示了LUAD的细胞异质性,并开发出一种新的癌症干性评估指标和4基因特征,作为评估LUAD对免疫检查点阻断疗法(ICB)或抗肿瘤疗法反应的潜在工具。
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来源期刊
Current stem cell research & therapy
Current stem cell research & therapy CELL & TISSUE ENGINEERING-CELL BIOLOGY
CiteScore
4.20
自引率
3.70%
发文量
197
审稿时长
>12 weeks
期刊介绍: Current Stem Cell Research & Therapy publishes high quality frontier reviews, drug clinical trial studies and guest edited issues on all aspects of basic research on stem cells and their uses in clinical therapy. The journal is essential reading for all researchers and clinicians involved in stem cells research.
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