Trans-omics biomarker model improves prognostic prediction accuracy for early-stage lung adenocarcinoma
Trans-omics biomarker model improves prognostic prediction accuracy for early-stage lung adenocarcinoma
复制标题
跨组学生物标志物模型提高了早期肺腺癌的预后预测准确性。
DOI:
10.18632/aging.102189
复制
发表时间:
2019-08-31
期刊:
影响因子:
5.2
通讯作者:
Christiani, David C.
中科院分区:
文献类型:
--
作者:
Dong, Xuesi;Zhang, Ruyang;Christiani, David C.
Limited studies have focused on developing prognostic models with trans-omics biomarkers for early-stage lung adenocarcinoma (LUAD). We performed integrative analysis of clinical information, DNA methylation, and gene expression data using 825 early-stage LUAD patients from 5 cohorts. Ranger algorithm was used to screen prognosis-associated biomarkers, which were confirmed with a validation phase. Clinical and biomarker information was fused using an iCluster plus algorithm, which significantly distinguished patients into hig-hand low-mortality risk groups (P-discovery = 0.01 and P-validation = 2.71x10(-3)). Further, potential functional DNA methylation-gene expression-overall survival pathways were evaluated by causal mediation analysis. The effect of DNA methylation level on LUAD survival was significantly mediated through gene expression level. By adding DNA methylation and gene expression biomarkers to a model of only clinical data, the AUCs of the trans-omics model improved by 18.3% (to 87.2%) and 16.4% (to 85.3%) in discovery and validation phases, respectively. Further, concordance index of the nomogram was 0.81 and 0.77 in discovery and validation phases, respectively. Based on systematic review of published literatures, our model was superior to all existing models for early-stage LUAD. In summary, our trans-omics model may help physicians accurately identify patients with high mortality risk.