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MicroRNAs expression profile in solid and unicystic ameloblastomas
OBJECTIVES: Odontogenic tumors (OT) represent a specific pathological category that includes some lesions with unpredictable biological behavior. Although most of these lesions are benign, some, such as the ameloblastoma, exhibit local aggressiveness and high recurrence rates. The most common types...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650163/ https://www.ncbi.nlm.nih.gov/pubmed/29053755 http://dx.doi.org/10.1371/journal.pone.0186841 |
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author | Setién-Olarra, A. Marichalar-Mendia, X. Bediaga, N. G. Aguirre-Echebarria, P. Aguirre-Urizar, J. M. Mosqueda-Taylor, A. |
author_facet | Setién-Olarra, A. Marichalar-Mendia, X. Bediaga, N. G. Aguirre-Echebarria, P. Aguirre-Urizar, J. M. Mosqueda-Taylor, A. |
author_sort | Setién-Olarra, A. |
collection | PubMed |
description | OBJECTIVES: Odontogenic tumors (OT) represent a specific pathological category that includes some lesions with unpredictable biological behavior. Although most of these lesions are benign, some, such as the ameloblastoma, exhibit local aggressiveness and high recurrence rates. The most common types of ameloblastoma are the solid/multicystic (SA) and the unicystic ameloblastoma (UA); the latter considered a much less aggressive entity as compared to the SA. The microRNA system regulates the expression of many human genes while its deregulation has been associated with neoplastic development. The aim of the current study was to determine the expression profiles of microRNAs present in the two most common types of ameloblastomas. MATERIAL & METHODS: MicroRNA expression profiles were assessed using TaqMan® Low Density Arrays (TLDAs) in 24 samples (8 SA, 8 UA and 8 control samples). The findings were validated using quantitative RTqPCR in an independent cohort of 19 SA, 8 UA and 19 dentigerous cysts as controls. RESULTS: We identified 40 microRNAs differentially regulated in ameloblastomas, which are related to neoplastic development and differentiation, and with the osteogenic process. Further validation of the top ranked microRNAs revealed significant differences in the expression of 6 of them in relation to UA, 7 in relation to SA and 1 (miR-489) that was related to both types. CONCLUSION: We identified a new microRNA signature for the ameloblastoma and for its main types, which may be useful to better understand the etiopathogenesis of this neoplasm. In addition, we identified a microRNA (miR-489) that is suggestive of differentiating among solid from unicystic ameloblastoma. |
format | Online Article Text |
id | pubmed-5650163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-56501632017-11-03 MicroRNAs expression profile in solid and unicystic ameloblastomas Setién-Olarra, A. Marichalar-Mendia, X. Bediaga, N. G. Aguirre-Echebarria, P. Aguirre-Urizar, J. M. Mosqueda-Taylor, A. PLoS One Research Article OBJECTIVES: Odontogenic tumors (OT) represent a specific pathological category that includes some lesions with unpredictable biological behavior. Although most of these lesions are benign, some, such as the ameloblastoma, exhibit local aggressiveness and high recurrence rates. The most common types of ameloblastoma are the solid/multicystic (SA) and the unicystic ameloblastoma (UA); the latter considered a much less aggressive entity as compared to the SA. The microRNA system regulates the expression of many human genes while its deregulation has been associated with neoplastic development. The aim of the current study was to determine the expression profiles of microRNAs present in the two most common types of ameloblastomas. MATERIAL & METHODS: MicroRNA expression profiles were assessed using TaqMan® Low Density Arrays (TLDAs) in 24 samples (8 SA, 8 UA and 8 control samples). The findings were validated using quantitative RTqPCR in an independent cohort of 19 SA, 8 UA and 19 dentigerous cysts as controls. RESULTS: We identified 40 microRNAs differentially regulated in ameloblastomas, which are related to neoplastic development and differentiation, and with the osteogenic process. Further validation of the top ranked microRNAs revealed significant differences in the expression of 6 of them in relation to UA, 7 in relation to SA and 1 (miR-489) that was related to both types. CONCLUSION: We identified a new microRNA signature for the ameloblastoma and for its main types, which may be useful to better understand the etiopathogenesis of this neoplasm. In addition, we identified a microRNA (miR-489) that is suggestive of differentiating among solid from unicystic ameloblastoma. Public Library of Science 2017-10-20 /pmc/articles/PMC5650163/ /pubmed/29053755 http://dx.doi.org/10.1371/journal.pone.0186841 Text en © 2017 Setién-Olarra et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Setién-Olarra, A. Marichalar-Mendia, X. Bediaga, N. G. Aguirre-Echebarria, P. Aguirre-Urizar, J. M. Mosqueda-Taylor, A. MicroRNAs expression profile in solid and unicystic ameloblastomas |
title | MicroRNAs expression profile in solid and unicystic ameloblastomas |
title_full | MicroRNAs expression profile in solid and unicystic ameloblastomas |
title_fullStr | MicroRNAs expression profile in solid and unicystic ameloblastomas |
title_full_unstemmed | MicroRNAs expression profile in solid and unicystic ameloblastomas |
title_short | MicroRNAs expression profile in solid and unicystic ameloblastomas |
title_sort | micrornas expression profile in solid and unicystic ameloblastomas |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650163/ https://www.ncbi.nlm.nih.gov/pubmed/29053755 http://dx.doi.org/10.1371/journal.pone.0186841 |
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