| Literature DB >> 28727484 |
Shuangchun Ren1, Zhuoyuan Xin1, Yinyan Xu1, Jianting Xu2, Guoqing Wang1,3.
Abstract
Liver cancer is the sixth most prevalent cancer, and the third most frequent cause of cancer-related deaths. Circular RNAs (circRNAs), a kind of special endogenous ncRNAs, have been coming back to the forefront of cancer genomics research. In this study, we used a systems biology approach to construct and analyze the circRNA molecular regulatory networks in the context of liver cancer. We detected a total of 127 differentially expressed circRNAs and 3,235 differentially expressed mRNAs. We selected the top-5 upregulated circRNAs to construct a circRNA-miRNA-mRNA network. We enriched the pathways and gene ontology items and determined their participation in cancer-related pathways such as p53 signaling pathway and pathways involved in angiogenesis and cell cycle. Quantitative real-time PCR was performed to verify the top-five circRNAs. ROC analysis showed circZFR, circFUT8, circIPO11 could significantly distinguish the cancer samples, with an AUC of 0.7069, 0.7575, and 0.7103, respectively. Our results suggest the circRNA-miRNA-mRNA network may help us further understand the molecular mechanisms of tumor progression in liver cancer, and reveal novel biomarkers and therapeutic targets.Entities:
Keywords: CircRNAs; circRNA-miRNA-mRNA; expression profile; liver cancer
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Year: 2017 PMID: 28727484 PMCID: PMC5736333 DOI: 10.1080/15384101.2017.1346754
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534