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FAF1 Gene Involvement in Pituitary Corticotroph Tumors.

Authors :
Nguyen M
Maria AG
Faucz FR
Trivellin G
Stratakis CA
Tatsi C
Source :
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme [Horm Metab Res] 2024 Aug; Vol. 56 (8), pp. 604-610. Date of Electronic Publication: 2023 Dec 08.
Publication Year :
2024

Abstract

Cushing's disease (CD) is caused by rare pituitary corticotroph tumors that lead to corticotropin (ACTH) excess. Variants in FAF1 , a pro-apoptotic protein involved in FAS-induced cell death, have been implicated in malignant disorders but the involvement of FAF1 in pituitary tumors has not been studied. Genetic data from patients with CD were reviewed for variants in FAF1 gene. Knockout mice (KO) were followed to assess the development of any pituitary disorder or cortisol excess. AtT-20 cells were used to study the effects of the variants of interest on ACTH secretion and cell proliferation. Three variants of interest were identified in 5 unique patients, two of which had rare allele frequency in genomic databases and were predicted to be likely pathogenic. KO mice were followed over time and no difference in their length/weight was noted. Additionally, KO mice did not develop any pituitary lesions and retained similar corticosterone secretion with wild type. AtT-20 cells transfected with FAF1 variants of interest or WT expression plasmids showed no significant difference in cell death or Pomc gene expression. However, in silico prediction models suggested significant differences in secondary structures of the produced proteins. In conclusion, we identified two FAF1 variants in patients diagnosed with CD with a potential pathogenic effect on the protein function and structure. Our in vitro and in vivo studies did not reveal an association of FAF1 defects with pituitary tumorigenesis and further studies may be needed to understand any association.<br />Competing Interests: CAS, FRF, and GT hold a patent on GPR101 and its function (US Patent No. 10,350,273, Treatment of Hormonal Disorders of Growth). CAS also holds patents on the function of the PRKAR1A and PDE11A genes and related issues; his laboratory had received research funding on the GPR101 gene, and on abnormal growth hormone secretion and its treatment by Pfizer, Inc. CAS is currently employed by ELPEN, SA and has been consulting for Lundbeck Pharmaceuticals and Sync, SA. CT received research funding on treatment of abnormal growth hormone secretion by Pfizer, Inc.<br /> (Thieme. All rights reserved.)

Details

Language :
English
ISSN :
1439-4286
Volume :
56
Issue :
8
Database :
MEDLINE
Journal :
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme
Publication Type :
Academic Journal
Accession number :
38065537
Full Text :
https://doi.org/10.1055/a-2192-1761