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Nat Commun ; 14(1): 5826, 2023 09 25.
Article in English | MEDLINE | ID: mdl-37749094

ABSTRACT

Reninomas are exceedingly rare renin-secreting kidney tumours that derive from juxtaglomerular cells, specialised smooth muscle cells that reside at the vascular inlet of glomeruli. They are the central component of the juxtaglomerular apparatus which controls systemic blood pressure through the secretion of renin. We assess somatic changes in reninoma and find structural variants that generate canonical activating rearrangements of, NOTCH1 whilst removing its negative regulator, NRARP. Accordingly, in single reninoma nuclei we observe excessive renin and NOTCH1 signalling mRNAs, with a concomitant non-excess of NRARP expression. Re-analysis of previously published reninoma bulk transcriptomes further corroborates our observation of dysregulated Notch pathway signalling in reninoma. Our findings reveal NOTCH1 rearrangements in reninoma, therapeutically targetable through existing NOTCH1 inhibitors, and indicate that unscheduled Notch signalling may be a disease-defining feature of reninoma.


Subject(s)
Kidney Neoplasms , Renin , Humans , Renin/metabolism , Kidney Neoplasms/metabolism , Juxtaglomerular Apparatus/metabolism , Juxtaglomerular Apparatus/pathology , Kidney Glomerulus/pathology , Signal Transduction/genetics , Receptor, Notch1/genetics
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