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Identification of aberrant microRNA expression pattern in pediatric gliomas by microarray
BACKGROUND: Brain tumor remains the leading cause of disease-related death in children. Many studies have focused on the complex biological process involved in pediatric brain tumors but little is know about the possible role of microRNAs in the genesis of these tumors. METHODS: In this study, we us...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853583/ https://www.ncbi.nlm.nih.gov/pubmed/24053158 http://dx.doi.org/10.1186/1746-1596-8-158 |
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author | Liu, Fatao Xiong, Yuyu Zhao, Yang Tao, Liming Zhang, Zhou Zhang, Hong Liu, Yun Feng, Guoyin Li, Baojie He, Lin Ma, Jie Qin, Shengying Yang, Yifeng |
author_facet | Liu, Fatao Xiong, Yuyu Zhao, Yang Tao, Liming Zhang, Zhou Zhang, Hong Liu, Yun Feng, Guoyin Li, Baojie He, Lin Ma, Jie Qin, Shengying Yang, Yifeng |
author_sort | Liu, Fatao |
collection | PubMed |
description | BACKGROUND: Brain tumor remains the leading cause of disease-related death in children. Many studies have focused on the complex biological process involved in pediatric brain tumors but little is know about the possible role of microRNAs in the genesis of these tumors. METHODS: In this study, we used a microRNA microarray assay to study the expression pattern of microRNAs in pediatric gliomas and matched normal tissues. RESULTS: We found 40 differentially expressed microRNAs, among which miR-1321, miR-513b, miR-769-3p were found be related to cancer genesis for the first time. The expression of selected microRNAs were then confirmed by qRT-PCR. Furthermore, GO and pathway analysis showed that the target genes of the 40 differentially expressed microRNAs were significantly enriched in nervous system-related and tumor-related biological processes and signaling pathways. Additionally, an apoptosis-related network of microRNA–mRNA interaction, representing the critical microRNAs and their targets, was constructed based on microRNA status. CONCLUSIONS: In the present study we identified the changed expression pattern of microRNAs in pediatric gliamas. Our study also provides a better understanding of pediatric brain tumor biology and may assist in the development of less toxic therapies and in the search for better markers for disease stratification. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1323049861105720 |
format | Online Article Text |
id | pubmed-3853583 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38535832013-12-07 Identification of aberrant microRNA expression pattern in pediatric gliomas by microarray Liu, Fatao Xiong, Yuyu Zhao, Yang Tao, Liming Zhang, Zhou Zhang, Hong Liu, Yun Feng, Guoyin Li, Baojie He, Lin Ma, Jie Qin, Shengying Yang, Yifeng Diagn Pathol Research BACKGROUND: Brain tumor remains the leading cause of disease-related death in children. Many studies have focused on the complex biological process involved in pediatric brain tumors but little is know about the possible role of microRNAs in the genesis of these tumors. METHODS: In this study, we used a microRNA microarray assay to study the expression pattern of microRNAs in pediatric gliomas and matched normal tissues. RESULTS: We found 40 differentially expressed microRNAs, among which miR-1321, miR-513b, miR-769-3p were found be related to cancer genesis for the first time. The expression of selected microRNAs were then confirmed by qRT-PCR. Furthermore, GO and pathway analysis showed that the target genes of the 40 differentially expressed microRNAs were significantly enriched in nervous system-related and tumor-related biological processes and signaling pathways. Additionally, an apoptosis-related network of microRNA–mRNA interaction, representing the critical microRNAs and their targets, was constructed based on microRNA status. CONCLUSIONS: In the present study we identified the changed expression pattern of microRNAs in pediatric gliamas. Our study also provides a better understanding of pediatric brain tumor biology and may assist in the development of less toxic therapies and in the search for better markers for disease stratification. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1323049861105720 BioMed Central 2013-09-20 /pmc/articles/PMC3853583/ /pubmed/24053158 http://dx.doi.org/10.1186/1746-1596-8-158 Text en Copyright © 2013 Liu et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Liu, Fatao Xiong, Yuyu Zhao, Yang Tao, Liming Zhang, Zhou Zhang, Hong Liu, Yun Feng, Guoyin Li, Baojie He, Lin Ma, Jie Qin, Shengying Yang, Yifeng Identification of aberrant microRNA expression pattern in pediatric gliomas by microarray |
title | Identification of aberrant microRNA expression pattern in pediatric gliomas by microarray |
title_full | Identification of aberrant microRNA expression pattern in pediatric gliomas by microarray |
title_fullStr | Identification of aberrant microRNA expression pattern in pediatric gliomas by microarray |
title_full_unstemmed | Identification of aberrant microRNA expression pattern in pediatric gliomas by microarray |
title_short | Identification of aberrant microRNA expression pattern in pediatric gliomas by microarray |
title_sort | identification of aberrant microrna expression pattern in pediatric gliomas by microarray |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853583/ https://www.ncbi.nlm.nih.gov/pubmed/24053158 http://dx.doi.org/10.1186/1746-1596-8-158 |
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