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Using microRNA Networks to Understand Cancer
Human cancers are characterized by deregulated expression of multiple microRNAs (miRNAs), involved in essential pathways that confer the malignant cells their tumorigenic potential. Each miRNA can regulate hundreds of messenger RNAs (mRNAs), while various miRNAs can control the same mRNA. Additional...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073868/ https://www.ncbi.nlm.nih.gov/pubmed/29949872 http://dx.doi.org/10.3390/ijms19071871 |
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author | Dragomir, Mihnea Mafra, Ana Carolina P. Dias, Sandra M. G. Vasilescu, Catalin Calin, George A. |
author_facet | Dragomir, Mihnea Mafra, Ana Carolina P. Dias, Sandra M. G. Vasilescu, Catalin Calin, George A. |
author_sort | Dragomir, Mihnea |
collection | PubMed |
description | Human cancers are characterized by deregulated expression of multiple microRNAs (miRNAs), involved in essential pathways that confer the malignant cells their tumorigenic potential. Each miRNA can regulate hundreds of messenger RNAs (mRNAs), while various miRNAs can control the same mRNA. Additionally, many miRNAs regulate and are regulated by other species of non-coding RNAs, such as circular RNAs (circRNAs) and long non-coding RNAs (lncRNAs). For this reason, it is extremely difficult to predict, study, and analyze the precise role of a single miRNA involved in human cancer, considering the complexity of its connections. Focusing on a single miRNA molecule represents a limited approach. Additional information could come from network analysis, which has become a common tool in the biological field to better understand molecular interactions. In this review, we focus on the main types of networks (monopartite, association networks and bipartite) used for analyzing biological data related to miRNA function. We briefly present the important steps to take when generating networks, illustrating the theory with published examples and with future perspectives of how this approach can help to better select miRNAs that can be therapeutically targeted in cancer. |
format | Online Article Text |
id | pubmed-6073868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60738682018-08-13 Using microRNA Networks to Understand Cancer Dragomir, Mihnea Mafra, Ana Carolina P. Dias, Sandra M. G. Vasilescu, Catalin Calin, George A. Int J Mol Sci Review Human cancers are characterized by deregulated expression of multiple microRNAs (miRNAs), involved in essential pathways that confer the malignant cells their tumorigenic potential. Each miRNA can regulate hundreds of messenger RNAs (mRNAs), while various miRNAs can control the same mRNA. Additionally, many miRNAs regulate and are regulated by other species of non-coding RNAs, such as circular RNAs (circRNAs) and long non-coding RNAs (lncRNAs). For this reason, it is extremely difficult to predict, study, and analyze the precise role of a single miRNA involved in human cancer, considering the complexity of its connections. Focusing on a single miRNA molecule represents a limited approach. Additional information could come from network analysis, which has become a common tool in the biological field to better understand molecular interactions. In this review, we focus on the main types of networks (monopartite, association networks and bipartite) used for analyzing biological data related to miRNA function. We briefly present the important steps to take when generating networks, illustrating the theory with published examples and with future perspectives of how this approach can help to better select miRNAs that can be therapeutically targeted in cancer. MDPI 2018-06-26 /pmc/articles/PMC6073868/ /pubmed/29949872 http://dx.doi.org/10.3390/ijms19071871 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Dragomir, Mihnea Mafra, Ana Carolina P. Dias, Sandra M. G. Vasilescu, Catalin Calin, George A. Using microRNA Networks to Understand Cancer |
title | Using microRNA Networks to Understand Cancer |
title_full | Using microRNA Networks to Understand Cancer |
title_fullStr | Using microRNA Networks to Understand Cancer |
title_full_unstemmed | Using microRNA Networks to Understand Cancer |
title_short | Using microRNA Networks to Understand Cancer |
title_sort | using microrna networks to understand cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073868/ https://www.ncbi.nlm.nih.gov/pubmed/29949872 http://dx.doi.org/10.3390/ijms19071871 |
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