Analysis of lncRNA-Associated ceRNA Network Reveals Potential lncRNA Biomarkers in Human Colon Adenocarcinoma

被引:94
作者
Zhang, Zhiyuan [1 ,2 ]
Qian, Wenwei [1 ,2 ]
Wang, Sen [1 ,2 ]
Ji, Dongjian [1 ,2 ]
Wang, Qingyuan [1 ,2 ]
Li, Jie [1 ,2 ]
Peng, Wen [1 ,2 ]
Gu, Jiou [1 ,2 ]
Hu, Tao [1 ,2 ]
Ji, Bing [1 ,2 ]
Zhang, Yue [1 ,2 ]
Wang, Shijia [1 ,2 ]
Sun, Yueming [2 ]
机构
[1] Nanjing Med Univ, Sch Clin Med 1, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Dept Gen Surg, Affiliated Hosp 1, Nanjing, Jiangsu, Peoples R China
关键词
Colon adenocarcinoma; LncRNA; ceRNA network; Biomarkers; Bioinformatics analysis; LONG NONCODING RNA; COLORECTAL-CARCINOMA PROGRESSION; CELL-PROLIFERATION; CANCER-CELLS; EXPRESSION; APOPTOSIS; PATHWAY; METASTASIS; INHIBITION; INVASION;
D O I
10.1159/000493623
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background/Aims: Long non-coding RNAs (lncRNAs) acting as competing endogenous RNAs (ceRNAs) play significant roles in the development of tumors, but the functions of specific lncRNAs and lncRNA-related ceRNA networks have not been fully elucidated for colon adenocarcinoma (COAD). In this study, we aimed to clarify the lncRNA-microRNA (miRNA)mRNA ceRNA network and potential lncRNA biomarkers in COAD. Methods: We extracted data from The Cancer Genome Atlas (TCGA) and identified COAD-specific mRNAs, miRNAs, and lncRNAs. The biological processes in Gene Ontology (GO) and the Kyoto Encyclopedia of Genes and Genomes (KEGG) were analyzed for COAD-specific mRNAs. We then constructed a ceRNA network of COAD-specific mRNAs, miRNAs and lncRNAs and analyzed the correlation between expression patterns and clinical features of the lncRNAs involved. After identifying potential mRNA targets of 4 lncRNAs related to overall survival (OS), we conducted stepwise analysis of these targets through GO and KEGG. Using tissue samples from our own patients, we also verified certain analytical results using quantitative real-time PCR (qRT-PCR). Results: Data from 521 samples (480 tumor tissue and 41 adjacent non-tumor tissue samples) were extracted from TCGA A total of 258 specific lncRNAs, 206 specific miRNAs, and 1467 specific mRNAs were identified (absolute log(2) [fold change] >2, false discovery rate <0.01). Analysis of KEGG revealed that specific mRNAs were enriched in cancer-related pathways. The ceRNA network was constructed with 64 lncRNAs, 18 miRNAs, and 42 mRNAs. Among these lncRNAs involved in the network, 3 lncRNAs (LINC00355, HULC, and IGF2-AS) were confirmed to be associated with certain clinical features and 4 lncRNAs (HOTAIR, LINC00355, KCNQ1OT1, and TSSC1-IT1) were found to be negatively linked to OS (log-rank p < 0.05). KEGG showed that the potential m RNA targets of these 4 lncRNAs may be concentrated in the MAPK pathway. Certain results were validated by qRT-PCR. Conclusion: This study providing novel insights into the lncRNA-miRNA-mRNA ceRNA network and reveals potential lncRNA biomarkers in COAD. (C) 2018 The Author(s) Published by S. Karger AG, Basel
引用
收藏
页码:1778 / 1791
页数:14
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