The Construction and Comprehensive Prognostic Analysis of the LncRNA-Associated Competitive Endogenous RNAs Network in Colorectal Cancer

被引:8
|
作者
Li, Wei [1 ]
Yu, Weifang [2 ]
Jiang, Xia [1 ]
Gao, Xian [1 ]
Wang, Guiqi [1 ]
Jin, Xiaojing [3 ]
Zhao, Zengren [1 ]
Liu, Yuegeng [1 ]
机构
[1] Hebei Med Univ, Dept Gen Surg, Hebei Key Lab Colorectal Canc Precis Diag & Treat, Hosp 1, Shijiazhuang, Hebei, Peoples R China
[2] Hebei Med Univ, Dept Endoscopy Ctr, Hosp 1, Shijiazhuang, Hebei, Peoples R China
[3] Hebei Med Univ, Dept Emergency, Hosp 1, Shijiazhuang, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
colorectal cancer; differentially expressed RNAs; ceRNA network; overall survival; nomogram; LONG NONCODING RNA; PROMOTES MIGRATION; CERNA HYPOTHESIS; POOR-PROGNOSIS; SIGNATURE; INVASION; MECHANISMS; BIOMARKER; NOMOGRAM; SURVIVAL;
D O I
10.3389/fgene.2020.00583
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Competing endogenous RNAs (ceRNAs) are a newly proposed RNA interaction mechanism that has been associated with the tumorigenesis, metastasis, diagnosis, and predicting survival of various cancers. In this study, we constructed a ceRNA network in colorectal cancer (CRC). Then, we sought to develop and validate a composite clinicopathologic-genomic nomogram using The Cancer Genome Atlas (TCGA) database. To construct the ceRNA network in CRC, we analyzed the mRNAseq, miRNAseq data, and clinical information from TCGA database. LncRNA, miRNA, and mRNA signatures were identified to construct risk score as independent indicators of the prognostic value in CRC patients. A composite clinicopathologic-genomic nomogram was developed to predict the overall survival (OS). One hundred sixty-one CRC-specific lncRNAs, 97 miRNAs, and 161 mRNAs were identified to construct the ceRNA network. Multivariate Cox proportional hazards regression analysis indicated that nine-lncRNA signatures, eight-miRNA signatures, and five-mRNA signatures showed a significant prognostic value for CRC. Furthermore, a clinicopathologic-genomic nomogram was constructed in the primary cohort, which performed well in both the primary and validation sets. This study presents a nomogram that incorporates the CRC-specific ceRNA expression profile, clinical features, and pathological factors, which demonstrate its excellent differentiation and risk stratification in predicting OS in CRC patients.
引用
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页数:13
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