Department of Lymphohematology and Oncology, Jiangxi Cancer Hospital of Nanchang University, Nanchang, Jiangxi, China.
Department of Orthopedics, Jiangxi Cancer Hospital of Nanchang University, Nanchang, Jiangxi, China.
Biomed Res Int. 2020 Nov 5;2020:3813546. doi: 10.1155/2020/3813546. eCollection 2020.
An increasing number of studies have indicated that the abnormal expression of certain long noncoding RNAs (lncRNAs) is linked to the overall survival (OS) of patients with myeloma.
Gene expression data of myeloma patients were downloaded from the Gene Expression Omnibus (GEO) database (GSE4581 and GSE57317). Cox regression analysis, Kaplan-Meier, and receiver operating characteristic (ROC) analysis were performed to construct and validate the prediction model. Single sample gene set enrichment (ssGSEA) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis were used to predict the function of a specified lncRNA.
In this study, a seven-lncRNA signature was identified and used to construct a risk score system for myeloma prognosis. This system was used to stratify patients with different survival rates in the training set into high-risk and low-risk groups. Test set, the entire test set, the external validation set, and the myeloma subtype achieved the authentication of the results. In addition, functional enrichment analysis indicated that 7 prognostic lncRNAs may be involved in the tumorigenesis of myeloma through cancer-related pathways and biological processes. The results of the immune score showed that IF_I was negatively correlated with the risk score. Compared with the published gene signature, the 7-lncRNA model has a higher C-index (above 0.8).
In summary, our data provide evidence that seven lncRNAs could be used as independent biomarkers to predict the prognosis of myeloma, which also indicated that these 7 lncRNAs may be involved in the progression of myeloma.
越来越多的研究表明,某些长链非编码 RNA(lncRNA)的异常表达与骨髓瘤患者的总生存期(OS)有关。
从基因表达综合数据库(GEO)(GSE4581 和 GSE57317)下载骨髓瘤患者的基因表达数据。进行 Cox 回归分析、Kaplan-Meier 和受试者工作特征(ROC)分析,构建并验证预测模型。单样本基因集富集(ssGSEA)和京都基因与基因组百科全书(KEGG)分析用于预测特定 lncRNA 的功能。
本研究确定了一个七 lncRNA 特征,并用于构建骨髓瘤预后的风险评分系统。该系统用于将训练集中具有不同生存率的患者分为高危和低危组。在测试集中、整个测试集、外部验证集和骨髓瘤亚型中验证了结果。此外,功能富集分析表明,7 个预后 lncRNA 可能通过癌症相关途径和生物学过程参与骨髓瘤的发生。免疫评分的结果表明 IF_I 与风险评分呈负相关。与已发表的基因特征相比,7-lncRNA 模型具有更高的 C 指数(超过 0.8)。
总之,我们的数据提供了证据,表明七个 lncRNA 可以作为独立的生物标志物来预测骨髓瘤的预后,这也表明这 7 个 lncRNA 可能参与骨髓瘤的进展。