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Construction and analyses of the microRNA-target gene differential regulatory network in thyroid carcinoma
by
Liu, Yang
, Kang, Ying-ying
, Wang, Ming-Li
, Guo, Min
, Wang, Yan
, Cheng, Zhi-Feng
in
3' Untranslated regions
/ Apoptosis
/ Binding
/ Biology and life sciences
/ Cancer
/ Cell growth
/ Cell Line, Tumor
/ Cell Proliferation
/ Computer and Information Sciences
/ Computer programs
/ Construction
/ Correlation
/ Data bases
/ Down-Regulation
/ Endocrinology
/ ErbB-3 protein
/ Gene expression
/ Gene Regulatory Networks
/ Genes
/ Genetic aspects
/ Genomes
/ Hospitals
/ Humans
/ Incidence
/ Inhibition
/ Kinases
/ Malignancy
/ MicroRNA
/ MicroRNAs
/ MicroRNAs - genetics
/ miRNA
/ Modules
/ Networks
/ Oncology
/ Overexpression
/ Receptor, ErbB-3 - genetics
/ Ribonucleic acid
/ RNA
/ RNA, Small Interfering - genetics
/ Studies
/ Target recognition
/ Thyroid
/ Thyroid cancer
/ Thyroid carcinoma
/ Thyroid Neoplasms - genetics
/ Topology
/ Transcription
2017
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Construction and analyses of the microRNA-target gene differential regulatory network in thyroid carcinoma
by
Liu, Yang
, Kang, Ying-ying
, Wang, Ming-Li
, Guo, Min
, Wang, Yan
, Cheng, Zhi-Feng
in
3' Untranslated regions
/ Apoptosis
/ Binding
/ Biology and life sciences
/ Cancer
/ Cell growth
/ Cell Line, Tumor
/ Cell Proliferation
/ Computer and Information Sciences
/ Computer programs
/ Construction
/ Correlation
/ Data bases
/ Down-Regulation
/ Endocrinology
/ ErbB-3 protein
/ Gene expression
/ Gene Regulatory Networks
/ Genes
/ Genetic aspects
/ Genomes
/ Hospitals
/ Humans
/ Incidence
/ Inhibition
/ Kinases
/ Malignancy
/ MicroRNA
/ MicroRNAs
/ MicroRNAs - genetics
/ miRNA
/ Modules
/ Networks
/ Oncology
/ Overexpression
/ Receptor, ErbB-3 - genetics
/ Ribonucleic acid
/ RNA
/ RNA, Small Interfering - genetics
/ Studies
/ Target recognition
/ Thyroid
/ Thyroid cancer
/ Thyroid carcinoma
/ Thyroid Neoplasms - genetics
/ Topology
/ Transcription
2017
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Do you wish to request the book?
Construction and analyses of the microRNA-target gene differential regulatory network in thyroid carcinoma
by
Liu, Yang
, Kang, Ying-ying
, Wang, Ming-Li
, Guo, Min
, Wang, Yan
, Cheng, Zhi-Feng
in
3' Untranslated regions
/ Apoptosis
/ Binding
/ Biology and life sciences
/ Cancer
/ Cell growth
/ Cell Line, Tumor
/ Cell Proliferation
/ Computer and Information Sciences
/ Computer programs
/ Construction
/ Correlation
/ Data bases
/ Down-Regulation
/ Endocrinology
/ ErbB-3 protein
/ Gene expression
/ Gene Regulatory Networks
/ Genes
/ Genetic aspects
/ Genomes
/ Hospitals
/ Humans
/ Incidence
/ Inhibition
/ Kinases
/ Malignancy
/ MicroRNA
/ MicroRNAs
/ MicroRNAs - genetics
/ miRNA
/ Modules
/ Networks
/ Oncology
/ Overexpression
/ Receptor, ErbB-3 - genetics
/ Ribonucleic acid
/ RNA
/ RNA, Small Interfering - genetics
/ Studies
/ Target recognition
/ Thyroid
/ Thyroid cancer
/ Thyroid carcinoma
/ Thyroid Neoplasms - genetics
/ Topology
/ Transcription
2017
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Construction and analyses of the microRNA-target gene differential regulatory network in thyroid carcinoma
Journal Article
Construction and analyses of the microRNA-target gene differential regulatory network in thyroid carcinoma
2017
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Overview
Thyroid-carcinoma (THCA) is the most common malignancy with an increasing incidence. Recent evidence has emphasized the role of microRNA (miRNA) in THCA. However, knowledge concerning the roles of miRNAs in THCA is still limited. We therefore use a miRNA-target gene differential regulatory network (MGDRN) to identify key miRNAs and characterize their synergistic regulation in THCA. Both miRNA-target gene interactions from multiple databases and negative expression correlations between miRNA-target genes were used to characterize the interactions. Then, two regulatory networks involving normal and tumor conditions were constructed, respectively. The MGDRN was finally constructed using different interactions between the above two regulatory networks. By analyzing topological features of the MGDRN, four miRNAs (hsa-mir-152-3p, hsa-mir-148a, hsa-mir-130b and hsa-mir-15b) are identified as key miRNAs in THCA. Over-expression of mir-152-3p inhibited proliferation and colony formation of TPC-1 cells. Furthermore, mir-152-3p negatively regulated ERBB3 by binding to the 3'-UTR of ERBB3, and down-regulation of ERBB3 by small interfering (si)RNAs inhibited proliferation and colony formation of TPC-1 cells, indicating that mir-152-3p acted as an anti-tumor miRNA by negatively regulating ERBB3. Finally, two synergistically dysregulated modules were identified which may contribute to the initiation and progression of THCA. Overall, the results provided a better understanding of the molecular basis of THCA, and suggested novel treatment strategies for this cancer.
Publisher
Public Library of Science,Public Library of Science (PLoS)
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