# Strobilurin X acts as an anticancer drug by inhibiting protein synthesis and suppressing mitochondrial respiratory chain activity

**Authors:** Kenji Takahashi, Tomoya Tanaka, Atsushi Ishihara, Toshio Ohta

PMC · DOI: 10.1007/s12672-024-01041-w · Discover Oncology · 2024-05-20

## TL;DR

Strobilurin X shows anticancer effects by inhibiting mitochondrial function and protein synthesis in cancer cells.

## Contribution

This study reveals the novel dual mechanism of strobilurin X in inducing cancer cell toxicity.

## Key findings

- Strobilurin X significantly reduced the viability of A549 and HeLa cancer cells compared to normal fibroblasts.
- The compound inhibited mitochondrial respiratory chain activity and suppressed protein synthesis in cancer cells.
- Cytotoxicity was not rescued by uridine, methyl pyruvate, or N-acetyl cysteine, indicating a unique mechanism.

## Abstract

Strobilurins act as antifungal agents by inhibiting the mitochondrial respiratory chain. The cytotoxic activity of strobilurins, focusing on its anticancer activities, has been reported. However, the mechanisms involved in these activities remain unclear.

The cytotoxic effects of strobilurin X isolated from the mycelium of Mucidula. venosolamellata were examined in human cancer cell lines (A549 and HeLa) and normal fibroblasts (WI-38).

Strobilurin X significantly decreased the viability of A549 and HeLa cells compared to that in the WI-38 cells after 48 h of exposure. The EC50 values for cytotoxicity in the A549, HeLa, and WI-38 cells were 3.4, 5.4, and 16.8 μg/mL, respectively. Strobilurin X inhibited the mitochondrial respiratory chain and enhanced the release of lactate in the A549 cells. The IC50 value of strobilurin X against the mitochondrial respiratory chain complex III activity was 139.8 ng/mL. The cytotoxicity induced by strobilurin X was not completely rescued after adding uridine, methyl pyruvate, or N-acetyl cysteine. Furthermore, pharmacological approaches demonstrated that strobilurin X failed to modulate the mitogen-activated protein kinase family and phosphoinositide 3-kinase-Akt pathways; alternatively, it suppressed protein synthesis independent of uridine.

Strobilurin X induced cytotoxicity by blocking the mitochondrial respiratory chain and suppressing protein synthesis. These findings may aid in the development of novel anticancer drugs using strobilurins.

## Linked entities

- **Chemicals:** strobilurin X (PubChem CID 165341843), uridine (PubChem CID 6029), methyl pyruvate (PubChem CID 11748), N-acetyl cysteine (PubChem CID 12035)
- **Diseases:** cancer (MONDO:0004992)
- **Species:** Homo sapiens (taxon 9606), Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}
- **Diseases:** cancer (MESH:D009369), cytotoxic (MESH:D064420)
- **Chemicals:** N-acetyl cysteine (MESH:D000111), lactate (MESH:D019344), respiratory chain complex III (-), Strobilurins (MESH:D000073739), uridine (MESH:D014529), methyl pyruvate (MESH:C104813)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mucidula (genus) [taxon 937601]
- **Cell lines:** WI-38 — Homo sapiens (Human), Finite cell line (CVCL_0579), HeLa — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_0030), A549 — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11106052/full.md

## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC11106052/full.md

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Source: https://tomesphere.com/paper/PMC11106052