Antisense Oligonucleotide-Mediated Polycystin 1 Upregulation by Enhancing PKD1 Translation Has the Potential to Treat ADPKD
Background: ADPKD is a genetic disorder characterized by cyst development and growth in the kidneys. Most ADPKD cases are caused by haploinsufficient mutations in the PKD1 gene, which encodes polycystin-1 (PC1). Thus, increasing PC1 protein levels represents a promising disease-modifying approach to address ADPKD at its root cause. This concept has been clinically validated by anti-miR-17 antisense oligonucleotides (ASOs), which indirectly upregulate PC1 expression. However, since individual microRNA can regulate multiple mRNAs, a more specific strategy is desirable. Methods: ASOs were designed using the Antisense-Coupled Translation Upregulation (ACT-UP1) technology developed at Arnatar. ASOs were delivered into different cells including ADPKD patient derived cells, and the effects on PC1 protein level, cAMP, Ca2+, and cyst development were analyzed. Potential off-target effect was evaluated using Western blotting and RNA sequencing. In vivo studies were conducted in male BALB/c mice, through subcutaneously injection. Results: The optimized ASO, ART5, increased PC1 protein levels by approximately 50% across various stable cell lines derived from human, mouse, and monkey. In patient-derived cells (WT9-7), ART5 increased PC1 protein levels by up to twofold, accompanied with reduced cAMP levels, decreased mTOR pathway activity, increased Ca2+ level, and diminished cyst formation. No off-target effects were detected, suggesting the high specificity of ART5. In vivo, ART5 administration increased PC1 protein levels up to 2 fold, with elevated PC1 levels persisting four weeks post-treatment. Conclusion: Together, our results demonstrate that the upregulatory ASO, ART5, specifically increases PC1 protein levels across multiple cell types and species by 50%-100%. The upregulated PC1 protein is functional, and ART5 treatment effectively inhibits cyst development. In vivo, ART5 exhibits high efficacy and a sustained pharmacodynamic effect, supporting the feasibility of less frequent clinical dosing. Collectively, these findings suggest that ART5 represents a promising therapeutic strategy for potential treatment of ADPKD. Funding: Commercial Support - Arnatar Therapeutics, Inc
Authors
- Ye Xu (ORCID: https://orcid.org/0000-0003-4322-244X)
- Xue‐hai Liang (ORCID: https://orcid.org/0000-0001-9333-8622)
- Hengbo Zhou (ORCID: https://orcid.org/0000-0002-9948-7909)
- Robert Thaï (ORCID: https://orcid.org/0000-0001-9438-4225)
- Lansha Peng
- Surendra Jain (ORCID: https://orcid.org/0000-0003-3859-1304)
- Yanfeng Wang (ORCID: https://orcid.org/0000-0002-3859-0937)
- Xiang Yu (ORCID: https://orcid.org/0000-0002-5730-8802)
- Jian Li (ORCID: https://orcid.org/0000-0002-4490-3530)
- Lingdi Zhang (ORCID: https://orcid.org/0000-0002-8671-1385)
Institutions
- Arisan Therapeutics (United States) (US)
Publication Details
- Journal
- Journal of the American Society of Nephrology
- Published
- 2025-10-01
- DOI
- https://doi.org/10.1681/asn.2025hpjwtmtc
- Primary Topic
- Genetic and Kidney Cyst Diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00