# ZYS-1 is not an ADAR1 inhibitor

**Authors:** Cassandra N. Smoak, Estelle N. Gardner, Renee N. Chua, Kyle A. Cottrell

PMC · DOI: 10.1261/rna.080721.125 · RNA · 2025-12-01

## TL;DR

This study shows that ZYS-1, claimed to be an ADAR1 inhibitor, does not specifically inhibit ADAR1 activity or function in cells.

## Contribution

The paper challenges the validity of ZYS-1 as a specific ADAR1 inhibitor through experimental validation.

## Key findings

- ZYS-1 is equally cytotoxic to ADAR1-dependent and ADAR1-independent cell lines.
- ZYS-1 does not reduce A-to-I editing at known ADAR1 sites or inhibit recombinant ADAR1 in vitro.
- ZYS-1 has minimal effect on PKR activation or IFN-stimulated gene induction.

## Abstract

Adenosine deaminase acting on RNA 1 (ADAR1) edits double-stranded RNA (dsRNA) substrates by the deamination of adenosine to inosine in a process known as A-to-I editing. Modulation of ADAR1 expression and editing activity has previously been described to play a role in cancer development and progression, with upregulation of ADAR1 being observed in a range of cancers. Further, depletion of ADAR1 leads to increased sensing of endogenous dsRNAs by dsRNA sensors in cell lines that require ADAR1 for survival, which are termed ADAR1-dependent. The activation of these sensors induces downstream production of type I interferons as well as translational inhibition and apoptosis. Therefore, ADAR1 is a promising oncologic therapeutic target. Recently, the small molecule ZYS-1 has been developed and presented as a direct inhibitor of ADAR1. We performed a series of in vitro and cellular experiments to validate the efficacy and specificity of ZYS-1 as an ADAR1 inhibitor. Evaluating the effect of ZYS-1 on cell viability revealed it to be equally cytotoxic to both ADAR1-dependent and ADAR1-independent cell lines, as well as wild-type and ADAR1 knockout cells. Moreover, ZYS-1 treatment had little effect on activation of PKR or induction of IFN stimulated genes. Importantly, treatment with ZYS-1 did not reduce cellular A-to-I editing for several known ADAR1 editing sites and did not inhibit in vitro A-to-I editing by recombinant ADAR1. Together, these data indicate that ZYS-1 is not a selective inhibitor of ADAR1.

## Linked entities

- **Genes:** ADAR (adenosine deaminase RNA specific) [NCBI Gene 103]
- **Proteins:** ADAR (adenosine deaminase RNA specific), EIF2AK2 (eukaryotic translation initiation factor 2 alpha kinase 2)
- **Chemicals:** ZYS-1 (PubChem CID 135421197)

## Full-text entities

- **Genes:** IFNA1 (interferon alpha 1) [NCBI Gene 3439] {aka IFL, IFN, IFN-ALPHA, IFN-alphaD, IFNA13, IFNA@}, ADAR (adenosine deaminase RNA specific) [NCBI Gene 103] {aka ADAR1, AGS6, DRADA, DSH, DSRAD, G1P1}, EIF2AK2 (eukaryotic translation initiation factor 2 alpha kinase 2) [NCBI Gene 5610] {aka PKR, PPP1R83, PRKR}
- **Diseases:** cancer (MESH:D009369)
- **Chemicals:** ZYS-1 (-), inosine (MESH:D007288), adenosine (MESH:D000241)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12621589/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12621589/full.md

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Source: https://tomesphere.com/paper/PMC12621589