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https://doi.org/10.1038/srep20065
Title: | Differentially Expressed miRNAs in Hepatocellular Carcinoma Target Genes in the Genetic Information Processing and Metabolism Pathways | Authors: | Thurnherr, T Mah, W.-C Lei, Z Jin, Y Rozen, S.G Lee, C.G |
Keywords: | messenger RNA microRNA transcriptome tumor marker adult aged biology cancer grading cancer staging energy metabolism female gene expression profiling gene expression regulation gene ontology gene regulatory network genetics human liver cell carcinoma liver tumor male metabolism middle aged molecular genetics pathology RNA interference signal transduction Adult Aged Biomarkers, Tumor Carcinoma, Hepatocellular Computational Biology Energy Metabolism Female Gene Expression Profiling Gene Expression Regulation, Neoplastic Gene Ontology Gene Regulatory Networks Humans Liver Neoplasms Male MicroRNAs Middle Aged Molecular Sequence Annotation Neoplasm Grading Neoplasm Staging RNA Interference RNA, Messenger Signal Transduction Transcriptome |
Issue Date: | 2016 | Citation: | Thurnherr, T, Mah, W.-C, Lei, Z, Jin, Y, Rozen, S.G, Lee, C.G (2016). Differentially Expressed miRNAs in Hepatocellular Carcinoma Target Genes in the Genetic Information Processing and Metabolism Pathways. Scientific Reports 6 : 20065. ScholarBank@NUS Repository. https://doi.org/10.1038/srep20065 | Abstract: | To date, studies of the roles of microRNAs (miRNAs) in hepatocellular carcinoma (HCC) have either focused on specific individual miRNAs and a small number of suspected targets or simply reported a list of differentially expressed miRNAs based on expression profiling. Here, we seek a more in-depth understanding of the roles of miRNAs and their targets in HCC by integrating the miRNA and messenger RNA (mRNA) expression profiles of tumorous and adjacent non-tumorous liver tissues of 100 HCC patients. We assessed the levels of 829 mature miRNAs, of which 32 were significantly differentially expressed. Statistical analysis indicates that six of these miRNAs regulate a significant proportion of their in silico predicted target mRNAs. Three of these miRNAs (miR-26a, miR-122, and miR-130a) were down-regulated in HCC, and their up-regulated gene targets are primarily associated with aberrant cell proliferation that involves DNA replication, transcription and nucleotide metabolism. The other three miRNAs (miR-21, miR-93, and miR-221) were up-regulated in HCC, and their down-regulated gene targets are primarily involved in metabolism and immune system processes. We further found evidence for a coordinated miRNA-induced regulation of important cellular processes, a finding to be considered when designing therapeutic applications based on miRNAs. © 2016, Nature Publishing Group. All rights reserved. | Source Title: | Scientific Reports | URI: | https://scholarbank.nus.edu.sg/handle/10635/174029 | ISSN: | 20452322 | DOI: | 10.1038/srep20065 |
Appears in Collections: | Elements Staff Publications |
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