1. Academic Validation
  2. Therapeutic RNA interference: A novel approach to the treatment of primary hyperoxaluria

Therapeutic RNA interference: A novel approach to the treatment of primary hyperoxaluria

  • Br J Clin Pharmacol. 2022 Jun;88(6):2525-2538. doi: 10.1111/bcp.14925.
Thomas A Forbes 1 2 3 Bob D Brown 4 Chengjung Lai 4
Affiliations

Affiliations

  • 1 Royal Children's Hospital, Parkville, Victoria, Australia.
  • 2 Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • 3 University of Melbourne, Parkville, Victoria, Australia.
  • 4 Dicerna Pharmaceuticals, Cambridge, MA, USA.
Abstract

RNA interference (RNAi) is a natural biological pathway that inhibits gene expression by targeted degradation or translational inhibition of cytoplasmic mRNA by the RNA induced silencing complex. RNAi has long been exploited in laboratory research to study the biological consequences of the reduced expression of a gene of interest. More recently RNAi has been demonstrated as a therapeutic avenue for rare metabolic diseases. This review presents an overview of the cellular RNAi machinery as well as therapeutic RNAi design and delivery. As a clinical example we present primary hyperoxaluria, an ultrarare inherited disease of increased hepatic oxalate production which leads to recurrent calcium oxalate kidney stones. In the most common form of the disease (Type 1), end-stage kidney disease occurs in childhood or young adulthood, often necessitating combined kidney and liver transplantation. In this context we discuss nedosiran (Dicerna Pharmaceuticals, Inc.) and lumasiran (Alnylam Pharmaceuticals), which are both novel RNAi therapies for primary hyperoxaluria that selectively reduce hepatic expression of Lactate Dehydrogenase and glycolate oxidase respectively, reducing hepatic oxalate production and urinary oxalate levels. Finally, we consider future optimizations advances in RNAi therapies.

Keywords

RNA interference; calcium oxalate; end-stage renal disease; glycolate oxidase; hyperoxaluria; kidney stones; lactate dehydrogenase; micro-RNA; primary hyperoxaluria; small interfering RNAs.

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