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

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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
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article

Antisense Oligonucleotide-Mediated Polycystin 1 Upregulation by Enhancing PKD1 Translation Has the Potential to Treat ADPKD

Ye Xu, Xue‐hai Liang, Hengbo Zhou, Robert Thaï et al.
Journal of the American Society of Nephrology
Genetic and Kidney Cyst Diseases
article

Antisense Oligonucleotide-Mediated Polycystin 1 Upregulation by Enhancing PKD1 Translation Has the Potential to Treat ADPKD

Ye Xu, Xue‐hai Liang, Hengbo Zhou, Robert Thaï, Lansha Peng, Surendra Jain, Yanfeng Wang, Xiang Yu, Jian Li, Lingdi Zhang
article en

Abstract

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

Journal of the American Society of NephrologyVol. 36(10S)
Arisan Therapeutics (United States) (US)
Openalex Percentile: Top 67%
Genetic and Kidney Cyst Diseases
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