| Literature DB >> 32327294 |
Mark R Woodford1, Sarah J Backe1, Rebecca A Sager2, Dimitra Bourboulia1, Gennady Bratslavsky1, Mehdi Mollapour3.
Abstract
Birt-Hogg-Dubé (BHD) and tuberous sclerosis (TS) syndromes share many clinical features. These two diseases display distinct histologic subtypes of renal tumors: chromophobe renal cell carcinoma and renal angiomyolipoma, respectively. Early work suggested a role for mTOR dysregulation in the pathogenesis of these two diseases, however their detailed molecular link remains elusive. Interestingly, a growing number of case reports describe renal angiomyolipoma in BHD patients, suggesting a common molecular origin. The BHD-associated proteins FNIP1/2 and the TS protein Tsc1 were recently identified as regulators of the molecular chaperone Hsp90. Dysregulation of Hsp90 activity has previously been reported to support tumorigenesis, providing a potential explanation for the overlapping phenotypic manifestations in these two hereditary syndromes.Entities:
Keywords: Birt-Hogg-Dubé (BHD); Chaperones; FLCN; Heat Shock Protein-90; Renal Angiomyolipoma; Tsc1 (Hamartin); Tsc2 (Tuberin); Tuberous Sclerosis Complex (TSC)
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Year: 2020 PMID: 32327294 PMCID: PMC7572595 DOI: 10.1016/j.urolonc.2020.03.016
Source DB: PubMed Journal: Urol Oncol ISSN: 1078-1439 Impact factor: 2.954