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急性髓系白血病RNA结合蛋白相关预后模型的系统构建与验证

Systematic Construction and Validation of an RNA-Binding Protein-Associated Prognostic Model for Acute Myeloid Leukemia.

作者信息

Luo Hongwei, Zhang Yingchun, Hu Nan, He Yancheng, He Chengcheng

机构信息

People's Hospital of Mianzhu, Deyang, China.

People's Hospital of Zhongjiang, Deyang, China.

出版信息

Front Genet. 2021 Sep 24;12:715840. doi: 10.3389/fgene.2021.715840. eCollection 2021.

Abstract

The abnormal expression of RNA-binding proteins (RBPs) in various malignant tumors is closely related to the occurrence and development of tumors. However, the role of RBPs in acute myeloid leukemia (AML) is unclear. We downloaded harmonized RNA-seq count data and clinical data for AML from UCSC Xena, including The Cancer Genome Atlas (TCGA), The Genotype-Tissue Expression (GTEx), and Therapeutically Applicable Research to Generate Effective Treatments (TARGET) cohorts. R package was used for differential expression analysis of 337 whole-blood data and 173 AML data. The prognostic value of these RBPs was systematically investigated by using univariate Cox regression analysis, least absolute shrinkage and selection operator (LASSO)-Cox regression analysis, and multivariate Cox regression analysis. C-index and calibration diagram were used to judge the accuracy of the model, and decision curve analysis (DCA) was used to judge the net benefit. The biological pathways involved were revealed by gene set enrichment analysis (GSEA). The Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis and the protein-protein interaction (PPI) network performed lateral verification on the selected gene set and LASSO results. A prognostic model of 12-RBP signature was established. In addition, the net benefit and prediction accuracy of the prognostic model and the mixed model based on it were significantly higher than that of cytogenetics. It is verified in the TARGET cohort and shows good prediction effect. Both the selection of our gene set and the LASSO results have high credibility. Most of these pathways are involved in the development of the disease, and they also accumulate in leukemia and RNA-related pathways. The prognosis model of the 12-RBP signature found in this study is an optimized biomarker that can effectively stratify the risk of AML patients. Nomogram based on this prognostic model is a reliable method to predict the median survival time of patients. This study expands our current understanding of the role of RBPs in the occurrence of AML and may lay the foundation for future treatment of the disease.

摘要

RNA结合蛋白(RBPs)在各种恶性肿瘤中的异常表达与肿瘤的发生发展密切相关。然而,RBPs在急性髓系白血病(AML)中的作用尚不清楚。我们从UCSC Xena下载了AML的协调RNA测序计数数据和临床数据,包括癌症基因组图谱(TCGA)、基因型-组织表达(GTEx)和治疗应用研究以生成有效治疗方法(TARGET)队列。使用R包对337份全血数据和173份AML数据进行差异表达分析。通过单变量Cox回归分析、最小绝对收缩和选择算子(LASSO)-Cox回归分析以及多变量Cox回归分析,系统地研究了这些RBPs的预后价值。使用C指数和校准图来判断模型的准确性,并使用决策曲线分析(DCA)来判断净效益。通过基因集富集分析(GSEA)揭示所涉及的生物学途径。基因本体论(GO)和京都基因与基因组百科全书(KEGG)途径分析以及蛋白质-蛋白质相互作用(PPI)网络对所选基因集和LASSO结果进行了横向验证。建立了12-RBP特征的预后模型。此外,预后模型和基于它的混合模型的净效益和预测准确性显著高于细胞遗传学。在TARGET队列中得到验证,显示出良好的预测效果。我们的基因集选择和LASSO结果都具有很高的可信度。这些途径大多参与疾病的发展,并且它们也在白血病和RNA相关途径中积累。本研究中发现的12-RBP特征的预后模型是一种优化的生物标志物,可以有效地对AML患者的风险进行分层。基于该预后模型的列线图是预测患者中位生存时间的可靠方法。本研究扩展了我们目前对RBPs在AML发生中作用的理解,并可能为该疾病的未来治疗奠定基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f468/8498117/2b6232e57ddd/fgene-12-715840-g001.jpg

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