# State of the ART: Drug Screening Reveals Artesunate as a Promising Anti-Fibrosis Therapy

**Authors:** Yujie Qiao, Jiurong Liang, Dianhua Jiang

PMC · DOI: 10.70322/jrbtm.2024.10023 · Journal of respiratory biology and translational medicine · 2025-03-01

## TL;DR

This study finds that artesunate, an existing drug, may be effective in treating fibrosis by targeting a specific signaling pathway.

## Contribution

The study identifies artesunate as a novel antifibrotic drug through drug screening in cardiac fibroblasts.

## Key findings

- Artesunate was identified as a potent antifibrotic drug using drug screening in cardiac fibroblasts.
- Artesunate targets the MD2/TLR4 signaling pathway to exert its antifibrotic effects.
- The study suggests repurposing existing drugs like artesunate for fibrosis treatment.

## Abstract

Fibrosis is a progressive pathological process that severely impairs
normal organ function. Current treatments for fibrosis are extremely limited,
with no curative approaches available. In a recent article published in
Cell, Zhang and colleagues employed drug screening using
ACTA2 reporter iPSC-derived cardiac fibroblasts and identified artesunate as a
potent antifibrotic drug by targeting MD2/TLR4 signaling. This study provides
new insights into strategies for exploiting existing drugs to treat
fibrosis.

## Linked entities

- **Genes:** ACTA2 (actin alpha 2, smooth muscle) [NCBI Gene 59], LY96 (lymphocyte antigen 96) [NCBI Gene 23643], TLR4 (toll like receptor 4) [NCBI Gene 7099]
- **Chemicals:** artesunate (PubChem CID 6917864)

## Full-text entities

- **Genes:** TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, LY96 (lymphocyte antigen 96) [NCBI Gene 23643] {aka ESOP-1, MD-2, MD2, ly-96}, ACTA2 (actin alpha 2, smooth muscle) [NCBI Gene 59] {aka ACTSA, SMDYS}
- **Diseases:** Anti-Fibrosis (MESH:D005355)

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC11800322/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC11800322/full.md

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Source: https://tomesphere.com/paper/PMC11800322