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Epigenetic Mechanisms Leading to Overexpression of HMGA Proteins in Human Pituitary Adenomas
Overexpression of the high-mobility group A (HMGA)1 and HMGA2 proteins is a feature of all human pituitary adenoma (PAs) subtypes. However, amplification and/or rearrangement of the HMGA2 have been described in human prolactinomas, but rarely in other pituitary subtypes, and no genomic amplification...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469109/ https://www.ncbi.nlm.nih.gov/pubmed/26137461 http://dx.doi.org/10.3389/fmed.2015.00039 |
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author | D’Angelo, Daniela Esposito, Francesco Fusco, Alfredo |
author_facet | D’Angelo, Daniela Esposito, Francesco Fusco, Alfredo |
author_sort | D’Angelo, Daniela |
collection | PubMed |
description | Overexpression of the high-mobility group A (HMGA)1 and HMGA2 proteins is a feature of all human pituitary adenoma (PAs) subtypes. However, amplification and/or rearrangement of the HMGA2 have been described in human prolactinomas, but rarely in other pituitary subtypes, and no genomic amplification of HMGA1 was detected in PAs. Here, we summarize the functional role of HMGA proteins in pituitary tumorigenesis and the epigenetic mechanisms contributing to HMGA overexpression in these tumors focusing on recent studies indicating a critical role of non-coding RNAs in modulating HMGA protein levels. |
format | Online Article Text |
id | pubmed-4469109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-44691092015-07-01 Epigenetic Mechanisms Leading to Overexpression of HMGA Proteins in Human Pituitary Adenomas D’Angelo, Daniela Esposito, Francesco Fusco, Alfredo Front Med (Lausanne) Medicine Overexpression of the high-mobility group A (HMGA)1 and HMGA2 proteins is a feature of all human pituitary adenoma (PAs) subtypes. However, amplification and/or rearrangement of the HMGA2 have been described in human prolactinomas, but rarely in other pituitary subtypes, and no genomic amplification of HMGA1 was detected in PAs. Here, we summarize the functional role of HMGA proteins in pituitary tumorigenesis and the epigenetic mechanisms contributing to HMGA overexpression in these tumors focusing on recent studies indicating a critical role of non-coding RNAs in modulating HMGA protein levels. Frontiers Media S.A. 2015-06-08 /pmc/articles/PMC4469109/ /pubmed/26137461 http://dx.doi.org/10.3389/fmed.2015.00039 Text en Copyright © 2015 D’Angelo, Esposito and Fusco. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine D’Angelo, Daniela Esposito, Francesco Fusco, Alfredo Epigenetic Mechanisms Leading to Overexpression of HMGA Proteins in Human Pituitary Adenomas |
title | Epigenetic Mechanisms Leading to Overexpression of HMGA Proteins in Human Pituitary Adenomas |
title_full | Epigenetic Mechanisms Leading to Overexpression of HMGA Proteins in Human Pituitary Adenomas |
title_fullStr | Epigenetic Mechanisms Leading to Overexpression of HMGA Proteins in Human Pituitary Adenomas |
title_full_unstemmed | Epigenetic Mechanisms Leading to Overexpression of HMGA Proteins in Human Pituitary Adenomas |
title_short | Epigenetic Mechanisms Leading to Overexpression of HMGA Proteins in Human Pituitary Adenomas |
title_sort | epigenetic mechanisms leading to overexpression of hmga proteins in human pituitary adenomas |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469109/ https://www.ncbi.nlm.nih.gov/pubmed/26137461 http://dx.doi.org/10.3389/fmed.2015.00039 |
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