Literature DB >> 29754632

Genetics of Cushing's Syndrome.

Laura C Hernández-Ramírez1, Constantine A Stratakis2.   

Abstract

The knowledge on the molecular and genetic causes of Cushing's syndrome (CS) has greatly increased in the recent years. Somatic mutations leading to overactive 3',5'-cyclic adenosine monophosphate/protein kinase A and wingless-type MMTV integration site family/beta-catenin pathways are the main molecular mechanisms underlying adrenocortical tumorigenesis. Corticotropinomas are characterized by resistance to glucocorticoid negative feedback, impaired cell cycle control and overexpression of pathways sustaining ACTH secretion. Recognizing the genetic defects behind corticotroph and adrenocortical tumorigenesis proves crucial for tailoring the clinical management of CS patients and for designing strategies for genetic counseling and clinical screening to be applied in routine medical practice. Published by Elsevier Inc.

Entities:  

Keywords:  ACTH; Adrenal hyperplasia; Corticotropinoma; Cushing’s syndrome; Glucocorticoids; Pituitary adenoma; USP8; cAMP

Mesh:

Year:  2018        PMID: 29754632      PMCID: PMC6029257          DOI: 10.1016/j.ecl.2018.02.007

Source DB:  PubMed          Journal:  Endocrinol Metab Clin North Am        ISSN: 0889-8529            Impact factor:   4.741


  154 in total

1.  PRKACB and Carney complex.

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2.  Study of a kindred with pheochromocytoma, medullary thyroid carcinoma, hyperparathyroidism and Cushing's disease: multiple endocrine neoplasia, type 2.

Authors:  A L Steiner; A D Goodman; S R Powers
Journal:  Medicine (Baltimore)       Date:  1968-09       Impact factor: 1.889

3.  Functional characterization of a rare germline mutation in the gene encoding the cyclin-dependent kinase inhibitor p27Kip1 (CDKN1B) in a Spanish patient with multiple endocrine neoplasia-like phenotype.

Authors:  Donatella Malanga; Silvia De Gisi; Miriam Riccardi; Marianna Scrima; Carmela De Marco; Mercedes Robledo; Giuseppe Viglietto
Journal:  Eur J Endocrinol       Date:  2011-11-30       Impact factor: 6.664

Review 4.  From β-catenin to ARM-repeat proteins in adrenocortical disorders.

Authors:  A Berthon; C A Stratakis
Journal:  Horm Metab Res       Date:  2014-10-08       Impact factor: 2.936

5.  Mice lacking p27(Kip1) display increased body size, multiple organ hyperplasia, retinal dysplasia, and pituitary tumors.

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Journal:  Cell       Date:  1996-05-31       Impact factor: 41.582

Review 6.  Familial isolated pituitary adenomas (FIPA) and the pituitary adenoma predisposition due to mutations in the aryl hydrocarbon receptor interacting protein (AIP) gene.

Authors:  Albert Beckers; Lauri A Aaltonen; Adrian F Daly; Auli Karhu
Journal:  Endocr Rev       Date:  2013-01-31       Impact factor: 19.871

7.  Molecular diagnosis of pituitary adenoma predisposition caused by aryl hydrocarbon receptor-interacting protein gene mutations.

Authors:  Marianthi Georgitsi; Anniina Raitila; Auli Karhu; Karoliina Tuppurainen; Markus J Mäkinen; Outi Vierimaa; Ralf Paschke; Wolfgang Saeger; Rob B van der Luijt; Timo Sane; Mercedes Robledo; Ernesto De Menis; Robert J Weil; Anna Wasik; Grzegorz Zielinski; Olga Lucewicz; Jan Lubinski; Virpi Launonen; Pia Vahteristo; Lauri A Aaltonen
Journal:  Proc Natl Acad Sci U S A       Date:  2007-02-28       Impact factor: 11.205

8.  Familial SDHA mutation associated with pituitary adenoma and pheochromocytoma/paraganglioma.

Authors:  Trisha Dwight; Kirsty Mann; Diana E Benn; Bruce G Robinson; Penny McKelvie; Anthony J Gill; Ingrid Winship; Roderick J Clifton-Bligh
Journal:  J Clin Endocrinol Metab       Date:  2013-04-30       Impact factor: 5.958

9.  Functional characterization of a CDKN1B mutation in a Sardinian kindred with multiple endocrine neoplasia type 4 (MEN4).

Authors:  Elena Pardi; Stefano Mariotti; Natalia S Pellegata; Katiuscia Benfini; Simona Borsari; Federica Saponaro; Liborio Torregrossa; Antonello Cappai; Chiara Satta; Marco Mastinu; Claudio Marcocci; Filomena Cetani
Journal:  Endocr Connect       Date:  2014-11-21       Impact factor: 3.335

10.  Identification of a novel RASD1 somatic mutation in a USP8-mutated corticotroph adenoma.

Authors:  Andrew V Uzilov; Khadeen C Cheesman; Marc Y Fink; Leah C Newman; Chetanya Pandya; Yelena Lalazar; Marco Hefti; Mary Fowkes; Gintaras Deikus; Chun Yee Lau; Aye S Moe; Yayoi Kinoshita; Yumi Kasai; Micol Zweig; Arpeta Gupta; Daniela Starcevic; Milind Mahajan; Eric E Schadt; Kalmon D Post; Michael J Donovan; Robert Sebra; Rong Chen; Eliza B Geer
Journal:  Cold Spring Harb Mol Case Stud       Date:  2017-05
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  5 in total

1.  Targeted Mutational Analysis of Cortisol-Producing Adenomas.

Authors:  Juilee Rege; Jessie Hoxie; Chia-Jen Liu; Morgan N Cash; James M Luther; Lan Gellert; Adina F Turcu; Tobias Else; Thomas J Giordano; Aaron M Udager; William E Rainey; Kazutaka Nanba
Journal:  J Clin Endocrinol Metab       Date:  2022-01-18       Impact factor: 6.134

2.  Concurrent mutations of germline GPR101 and somatic USP8 in a pediatric giant pituitary ACTH adenoma: a case report.

Authors:  Xu-Dong Bao; Lin Lu; Hui-Juan Zhu; Yong Yao; Ming Feng; Ren-Zhi Wang; Xiao Zhai; Yong Fu; Feng-Ying Gong; Zhao-Lin Lu
Journal:  BMC Endocr Disord       Date:  2022-06-06       Impact factor: 3.263

3.  Intratumoral steroid profiling of adrenal cortisol-producing adenomas by liquid chromatography- mass spectrometry.

Authors:  James P Teuber; Kazutaka Nanba; Adina F Turcu; Xuan Chen; Lili Zhao; Tobias Else; Richard J Auchus; William E Rainey; Juilee Rege
Journal:  J Steroid Biochem Mol Biol       Date:  2021-06-02       Impact factor: 5.011

4.  The genomic profiling and MAMLD1 expression in human and canines with Cushing's disease.

Authors:  Andrew Wang; Stewart G Neill; Scott Newman; Marianna A Tryfonidou; Adriana Ioachimescu; Michael R Rossi; Björn P Meij; Nelson M Oyesiku
Journal:  BMC Endocr Disord       Date:  2021-09-13       Impact factor: 2.763

5.  Mislocalization of protein kinase A drives pathology in Cushing's syndrome.

Authors:  Mitchell H Omar; Dominic P Byrne; Kiana N Jones; Tyler M Lakey; Kerrie B Collins; Kyung-Soon Lee; Leonard A Daly; Katherine A Forbush; Ho-Tak Lau; Martin Golkowski; G Stanley McKnight; David T Breault; Anne-Marie Lefrançois-Martinez; Antoine Martinez; Claire E Eyers; Geoffrey S Baird; Shao-En Ong; F Donelson Smith; Patrick A Eyers; John D Scott
Journal:  Cell Rep       Date:  2022-07-12       Impact factor: 9.995

  5 in total

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