An Integrated Three-Long Non-coding RNA Signature Predicts Prognosis in Colorectal Cancer Patients

被引:28
|
作者
Liu, Yuhang [1 ,2 ]
Liu, Bingxin [1 ,2 ]
Jin, Guoying [1 ,2 ]
Zhang, Jia [1 ,2 ]
Wang, Xue [2 ]
Feng, Yuyang [2 ]
Bian, Zehua [1 ,2 ]
Fei, Bojian [3 ]
Yin, Yuan [1 ,2 ]
Huang, Zhaohui [1 ,2 ]
机构
[1] Jiangnan Univ, Wuxi Canc Inst, Affiliated Hosp, Wuxi, Jiangsu, Peoples R China
[2] Jiangnan Univ, Lab Canc Epigenet, Wuxi Sch Med, Wuxi, Jiangsu, Peoples R China
[3] Jiangnan Univ, Dept Surg Oncol, Affiliated Hosp, Wuxi, Jiangsu, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2019年 / 9卷
基金
中国国家自然科学基金;
关键词
long non-coding RNA; overall survival; prognosis; biomarkers; training set; clinical validation set; PROLIFERATION; PREVENTION; MIGRATION;
D O I
10.3389/fonc.2019.01269
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Colorectal cancer (CRC) is one of the most common cancers worldwide, whose morbidity and mortality gradually increased. Here, we aimed to identify and access prognostic long non-coding RNAs (lncRNAs) associated with overall survival (OS) in CRC. Firstly, RNA expression profiles were obtained from The Cancer Genome Atlas (TCGA) database, and 439 CRC patients were enrolled as a training set. Univariate Cox analysis and the least absolute shrinkage and selection operator analysis (LASSO) were performed to identify the prognostic lncRNAs. Multivariable Cox regression analysis was used to establish a prognostic risk formula including three lncRNAs (AP003555.2, AP006284.1, and LINC01602). The low-risk group had a better OS than the high-risk group (P < 0.0001), and the areas under the receiver operating characteristic curve (AUCs) of 3- and 5-year OS were 0.712 and 0.674, respectively. Then, we evaluated the signature in a clinical validation set which were collected from the Affiliated Hospital of Jiangnan University. Compared with the low-risk group, patients' OS were found to be significantly worse in the high-risk group (P = 0.0057). The AUCs of 3- and 5-year OS were 0.701 and 0.694, respectively. Finally, we constructed an lncRNA-microRNA (miRNA)-messenger RNA (mRNA) competing endogenous RNA (ceRNA) network to explore the potential function of three differentially expressed lncRNAs (DElncRNAs). The Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis indicated that these DElncRNAs were involved with several cancer-related pathways. In summary, our data provide evidence that the three-lncRNA signature could serve as an independent biomarker to predict prognosis in CRC. This study will also suggest that these three lncRNAs potentially participate in the progression of CRC.
引用
收藏
页数:11
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