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Recent advances in understanding Cushing disease: resistance to glucocorticoid negative feedback and somatic USP8 mutations
Cushing’s disease is a rare disease with a characteristic phenotype due to significant hypercortisolism driven by over-secretion of adrenocorticotropic hormone and to high morbidity and mortality if untreated. It is caused by a corticotroph adenoma of the pituitary, but the exact mechanisms leading...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5414817/ https://www.ncbi.nlm.nih.gov/pubmed/28529722 http://dx.doi.org/10.12688/f1000research.10968.1 |
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author | Daniel, Eleni Newell-Price, John |
author_facet | Daniel, Eleni Newell-Price, John |
author_sort | Daniel, Eleni |
collection | PubMed |
description | Cushing’s disease is a rare disease with a characteristic phenotype due to significant hypercortisolism driven by over-secretion of adrenocorticotropic hormone and to high morbidity and mortality if untreated. It is caused by a corticotroph adenoma of the pituitary, but the exact mechanisms leading to tumorigenesis are not clear. Recent advances in molecular biology such as the discovery of somatic mutations of the ubiquitin-specific peptidase 8 ( USP8) gene allow new insights into the pathogenesis, which could be translated into exciting and much-needed therapeutic applications. |
format | Online Article Text |
id | pubmed-5414817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-54148172017-05-18 Recent advances in understanding Cushing disease: resistance to glucocorticoid negative feedback and somatic USP8 mutations Daniel, Eleni Newell-Price, John F1000Res Review Cushing’s disease is a rare disease with a characteristic phenotype due to significant hypercortisolism driven by over-secretion of adrenocorticotropic hormone and to high morbidity and mortality if untreated. It is caused by a corticotroph adenoma of the pituitary, but the exact mechanisms leading to tumorigenesis are not clear. Recent advances in molecular biology such as the discovery of somatic mutations of the ubiquitin-specific peptidase 8 ( USP8) gene allow new insights into the pathogenesis, which could be translated into exciting and much-needed therapeutic applications. F1000Research 2017-05-02 /pmc/articles/PMC5414817/ /pubmed/28529722 http://dx.doi.org/10.12688/f1000research.10968.1 Text en Copyright: © 2017 Daniel E and Newell-Price J http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Daniel, Eleni Newell-Price, John Recent advances in understanding Cushing disease: resistance to glucocorticoid negative feedback and somatic USP8 mutations |
title | Recent advances in understanding Cushing disease: resistance to glucocorticoid negative feedback and somatic USP8 mutations |
title_full | Recent advances in understanding Cushing disease: resistance to glucocorticoid negative feedback and somatic USP8 mutations |
title_fullStr | Recent advances in understanding Cushing disease: resistance to glucocorticoid negative feedback and somatic USP8 mutations |
title_full_unstemmed | Recent advances in understanding Cushing disease: resistance to glucocorticoid negative feedback and somatic USP8 mutations |
title_short | Recent advances in understanding Cushing disease: resistance to glucocorticoid negative feedback and somatic USP8 mutations |
title_sort | recent advances in understanding cushing disease: resistance to glucocorticoid negative feedback and somatic usp8 mutations |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5414817/ https://www.ncbi.nlm.nih.gov/pubmed/28529722 http://dx.doi.org/10.12688/f1000research.10968.1 |
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