Chemically inducible antisense oligonucleotides for cell-specific gene silencing
Cell-specific control of the function of antisense oligonucleotides (ASOs) is highly desirable for precise gene therapy while minimizing adverse effects in normal cells. Herein, we report a novel class of chemically inducible ASOs (iASOs) that achieve tumor-cell-selective gene silencing through hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>)-triggered activation. Through post-synthetic incorporation of phenylboronic acid (BO) caging groups at the backbone positions, we developed iASOs that remain functionally inactive until the H<sub>2</sub>O<sub>2</sub>-triggered removal of the BO groups caused activation. Using EGFP as a reporter system, we demonstrated that the optimal BO-modified iASO exhibited slight gene silencing activity in normal cells but achieved >80% knockdown of the target mRNA in tumor cells. The BO-modified iASO was further applied to target the endogenous Bcl<sub>2</sub> gene, demonstrating its ability for controlling gene silencing and inducing cell death. This study establishes a simple and effective platform for conditional gene regulation and the development of cell-specific ASO therapeutics.
Authors
- Zhenkun Wu (ORCID: https://orcid.org/0000-0001-6458-5659)
- Zhen Xun (ORCID: https://orcid.org/0000-0002-4242-3402)
- Lijuan Tang
- Yang Hai (ORCID: https://orcid.org/0000-0002-9420-0614)
- Jian‐Hui Jiang (ORCID: https://orcid.org/0000-0003-1594-4023)
Institutions
- Hunan University (CN)
Publication Details
- Journal
- RSC Chemical Biology
- Published
- 2025-01-01
- DOI
- https://doi.org/10.1039/d5cb00186b
- Primary Topic
- RNA Interference and Gene Delivery
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Chinese Academy of Sciences
- National Cancer Institute