Please use this identifier to cite or link to this item: 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

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_1038_srep20065.pdf2.39 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.