| Literature DB >> 33974998 |
Daryl Jin Tai Tay1, Yangyang Song1, Boya Peng2, Tan Boon Toh3, Lissa Hooi1, Desiree-Faye Kaixin Toh4, HuiQi Hong5, Sze Jing Tang1, Jian Han1, Wei Liang Gan1, Tim Hon Man Chan1, Manchugondanahalli S Krishna4, Kiran M Patil4, Manikantha Maraswami4, Teck Peng Loh4, Yock Young Dan6, Lei Zhou7, Glenn Kunnath Bonney8, Pierce Kah-Hoe Chow9, Gang Chen10, Edward Kai-Hua Chow11, Minh T N Le2, Leilei Chen12.
Abstract
Dysregulated adenosine-to-inosine (A-to-I) RNA editing is implicated in various cancers. However, no available RNA editing inhibitors have so far been developed to inhibit cancer-associated RNA editing events. Here, we decipher the RNA secondary structure of antizyme inhibitor 1 (AZIN1), one of the best-studied A-to-I editing targets in cancer, by locating its editing site complementary sequence (ECS) at the 3' end of exon 12. Chemically modified antisense oligonucleotides (ASOs) that target the editing region of AZIN1 caused a substantial exon 11 skipping, whereas ECS-targeting ASOs effectively abolished AZIN1 editing without affecting splicing and translation. We demonstrate that complete 2'-O-methyl (2'-O-Me) sugar ring modification in combination with partial phosphorothioate (PS) backbone modification may be an optimal chemistry for editing inhibition. ASO3.2, which targets the ECS, specifically inhibits cancer cell viability in vitro and tumor incidence and growth in xenograft models. Our results demonstrate that this AZIN1-targeting, ASO-based therapeutics may be applicable to a wide range of tumor types.Entities:
Keywords: A-to-I RNA editing; ADAR1; AZIN1; RNA editing inhibtion; RNA therapeutics; antisense oligonucleotides; cancer
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Year: 2021 PMID: 33974998 PMCID: PMC8571177 DOI: 10.1016/j.ymthe.2021.05.008
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454