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Immune-related lncRNAs as predictors of survival in breast cancer: a prognostic signature

机译:免疫相关的LNCRNA作为乳腺癌存活的预测因子:预后签名

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Breast cancer is a highly heterogeneous disease, this poses challenges for classification and management. Long non-coding RNAs play acrucial role in the breast cancersdevelopment and progression, especially in tumor-related immune processes which have become the most rapidly investigated area. Therefore, we aimed at developing an immune-related lncRNA signature to improve the prognosis prediction of breast cancer. We obtained breast cancer patient samples and corresponding clinical data from The Cancer Genome Atlas (TCGA) database. Immune-related lncRNAs were screened by co-expression analysis of immune-related genes which were downloaded from the Immunology Database and Analysis Portal (ImmPort). Clinical patient samples were randomly separated into training and testing sets. In the training set, univariate Cox regression analysis and LASSO regression were utilized to build a prognostic immune-related lncRNA signature. The signature was validated in the training set, testing set, and whole cohorts by the Kaplan–Meier log-rank test, time-dependent ROC curve analysis, principal component analysis, univariate andmultivariate Cox regression analyses. A total of 937 immune- related lncRNAs were identified, 15 candidate immune-related lncRNAs were significantly associated with overall survival (OS). Eight of these lncRNAs (OTUD6B-AS1, AL122010.1, AC136475.2, AL161646.1, AC245297.3, LINC00578, LINC01871, AP000442.2) were selected for establishment of the risk prediction model. The OS of patients in the low-risk group was higher than that of patients in the high-risk group (p?=?1.215e???06 in the training set; p?=?0.0069 in the validation set; p?=?1.233e???07 in whole cohort). The time-dependent ROC curve analysis revealed that the AUCs for OS in the first, eighth, and tenth year were 0.812, 0.81, and 0.857, respectively, in the training set, 0.615, 0.68, 0.655 in the validation set, and 0.725, 0.742, 0.741 in the total cohort. Multivariate Cox regression analysis indicated the model was a reliable and independent indicator for the prognosis of breast cancer in the training set (HR?=?1.432; 95% CI 1.204–1.702, p??0.001), validation set (HR?=?1.162; 95% CI 1.004–1.345, p?=?0.044), and whole set (HR?=?1.240; 95% CI 1.128–1.362, p??0.001). GSEA analysis revealed a strong connection between the signature and immune-related biological processes and pathways. We constructed and verified a robust signature of 8 immune-related lncRNAs for the prediction of breast cancer patient survival.
机译:乳腺癌是一种高度异质的疾病,这会带来分类和管理的挑战。长期非编码RNA在乳腺癌和进展中起神色作用,特别是在肿瘤相关的免疫过程中,该过程已成为最迅速调查的区域。因此,我们旨在开发免疫相关的LNCRNA签名,以改善乳腺癌的预后预测。我们从癌症基因组Atlas(TCGA)数据库中获得了乳腺癌患者样品和相应的临床资料。通过从免疫数据库和分析门户下载的免疫相关基因的共表达分析来筛选免疫相关的LNCRNA,从免疫数据库和分析门户(IMMOST)。临床患者样品随机分离成训练和测试组。在培训集中,利用单变量COX回归分析和套索回归来构建预后免疫相关的LNCRNA签名。通过Kaplan-Meier日志排名测试,时间依赖的ROC曲线分析,主成分分析,单变量和多变量Cox回归分析,签名在培训集,测试集和整个队列中验证了验证集,测试集和整个群组。鉴定了总共937个免疫相关的LNCRNA,与总存活(OS)显着相关的15个候选免疫相关的LNCRNA。选择其中八个(OTUD6B-AS1,AL1220101,AC136475.2,AL161646.1,AC245297.3,LINC00578,LINC01871,AP000442.2),用于建立风险预测模型。低风险群体的患者的OS高于高风险群体(P?= 1.215E)高风险患者(训练组中的06; P?= 0.0069在验证组中; P? =?在整个队列1.233e ??? 07)。时间依赖的ROC曲线分析显示,在验证组中分别为0.812,0.81和0.857的OS中的AUC,0.615,0.68,0.655,验证集,0.725,总队列中0.742,0.741。多变量Cox回归分析表明,该模型是培训集中乳腺癌预后的可靠和独立的指标(HR?=?1.432; 95%CI 1.204-1.702,P?<0.001),验证集(HR?= ?1.162; 95%CI 1.004-1.345,P?= 0.044)和整套(HR?=?1.240; 95%CI 1.128-1.362,P?<0.001)。 GSEA分析显示签名和免疫相关生物过程与途径之间的强烈联系。我们构建并验证了8个免疫相关LNCRNA的强大签名,以预测乳腺癌患者存活。

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