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Recent advances in understanding Cushing disease: resistance to glucocorticoid negative feedback and somatic USP8 mutations [version 1; referees: 2 approved]

Authors :
Eleni Daniel
John Newell-Price
Author Affiliations :
<relatesTo>1</relatesTo>Department of Oncology and Metabolism, University of Sheffield Medical School, Sheffield, UK
Source :
F1000Research. 6:F1000 Faculty Rev-613
Publication Year :
2017
Publisher :
London, UK: F1000 Research Limited, 2017.

Abstract

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.

Details

ISSN :
20461402
Volume :
6
Database :
F1000Research
Journal :
F1000Research
Notes :
Editorial Note on the Review Process F1000 Faculty Reviews are commissioned from members of the prestigious F1000 Faculty and are edited as a service to readers. In order to make these reviews as comprehensive and accessible as possible, the referees provide input before publication and only the final, revised version is published. The referees who approved the final version are listed with their names and affiliations but without their reports on earlier versions (any comments will already have been addressed in the published version). The referees who approved this article are: Marco Boscaro, Endocrinology Unit, Department of Medicine, Padova University Hospital, Padova, Italy No competing interests were disclosed. Richard Feelders, Erasmus Medical Center, Rotterdam, Netherlands No competing interests were disclosed., , [version 1; referees: 2 approved]
Publication Type :
Academic Journal
Accession number :
edsfor.10.12688.f1000research.10968.1
Document Type :
review
Full Text :
https://doi.org/10.12688/f1000research.10968.1