# Topoisomerase inhibitor amonafide enhances defense responses to promote longevity in C. elegans

**Authors:** Iman Man Hu, Ana Serna, Stacia Everts, Lale Güngördü, Bauke V. Schomakers, Ellen A. A. Nollen, Arwen W. Gao, Riekelt H. Houtkooper, Georges E. Janssens

PMC · DOI: 10.1007/s11357-025-01599-5 · GeroScience · 2025-03-14

## TL;DR

A drug called amonafide extends lifespan and healthspan in worms by activating defense pathways, and may help treat age-related diseases like Parkinson’s.

## Contribution

Amonafide is identified as a novel geroprotector that promotes longevity and healthspan through non-canonical pathways.

## Key findings

- Amonafide extends lifespan and improves healthspan in C. elegans.
- The drug activates defense pathways including UPRmt, immune response, and stress response.
- Amonafide improves mobility in a C. elegans model of Parkinson’s disease.

## Abstract

Aging is a major risk factor for disease, and developing effective pharmaceutical interventions to improve healthspan and promote longevity has become a high priority for society. One of the molecular pathways related to longevity in various model organisms revolves around lowering AKT1 levels. This prompted our in silico drug screen for small molecules capable of mimicking the transcriptional effects of AKT1 knockdown. We found topoisomerase inhibitors as a top candidate longevity-drug class. Evaluating multiple compounds from this class in C. elegans revealed that the topoisomerase inhibitor amonafide has the greatest benefit on healthspan and lifespan. Intriguingly, the longevity effect of amonafide was not solely dependent on DAF-16/FOXO, the canonical pathway for lifespan extension via AKT1 inhibition. We performed RNA-seq on amonafide-treated worms and revealed a more youthful transcriptional signature, including the activation of diverse molecular and cellular defense pathways. We found the mitochondrial unfolded protein response (UPRmt) regulator afts-1 to be crucial for both improved healthspan and extended lifespan upon amonafide treatment. Moreover, healthspan was partially dependent on the immune response transcription factor zip-2 and the integrated stress response transcription factor atf-4. We further examined the potential of amonafide in age-related disease. Treating a C. elegans model for Parkinson’s disease with amonafide improved mobility. In conclusion, we identified amonafide as a novel geroprotector, which activates mitochondrial-, pathogen-, and xenobiotic-associated defense responses that—though more studies are needed—may serve as a candidate for Parkinson’s disease therapy.

The online version contains supplementary material available at 10.1007/s11357-025-01599-5.

## Linked entities

- **Genes:** daf-16 (Forkhead box protein O) [NCBI Gene 172981], foxo (forkhead box, sub-group O) [NCBI Gene 41709], AFTS1 (Aldo-keto reductase AFTS1) [NCBI Gene 43620113], SLC39A2 (solute carrier family 39 member 2) [NCBI Gene 29986], ATF4 (activating transcription factor 4) [NCBI Gene 468]
- **Chemicals:** amonafide (PubChem CID 50515)
- **Diseases:** Parkinson’s disease (MONDO:0005180)

## Full-text entities

- **Genes:** daf-16 (Forkhead box protein O) [NCBI Gene 172981], akt-1 (Serine/threonine-protein kinase akt-1) [NCBI Gene 179424], zip-2 (Transcription factor zip-2) [NCBI Gene 175240]
- **Diseases:** age-related disease (MESH:D010024), Parkinson's disease (MESH:D010300)
- **Chemicals:** amonafide (MESH:C037020), healthspan (-)
- **Species:** C. elegans [taxon 328850]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12181488/full.md

## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12181488/full.md

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Source: https://tomesphere.com/paper/PMC12181488