PUBLICATION

Toosendanin-induced liver damage through irreparable DNA damage and autophagy flow blockade

Authors
Lin, Y., Zhang, J., Gao, X., Wu, Z., Yang, L., Tian, K., Lv, X., Li, J., Chen, K., Zhang, Y., Hu, H., Zhu, A.
ID
ZDB-PUB-250307-25
Date
2025
Source
Phytomedicine : international journal of phytotherapy and phytopharmacology   140: 156586156586 (Journal)
Registered Authors
Keywords
Cell cycle, DNA damage responses, Hepatotoxicity, Toosendanin
MeSH Terms
  • Cell Cycle Checkpoints/drug effects
  • Fruit/chemistry
  • Animals
  • Hep G2 Cells
  • DNA Damage*/drug effects
  • Drugs, Chinese Herbal/pharmacology
  • Triterpenes
  • Molecular Docking Simulation
  • Network Pharmacology
  • Autophagy*/drug effects
  • Zebrafish*
  • Humans
  • Reactive Oxygen Species*/metabolism
  • Chemical and Drug Induced Liver Injury*
  • Liver/drug effects
PubMed
40049104 Full text @ Phytomedicine
Abstract
The fruit of Melia toosendan Sieb. et Zucc. (MT) is known for its efficacy in relieving pain and treating roundworms. Toosendanin (TO) has been identified as a bioactive marker of MT, with hepatotoxic properties. This study offers a comprehensive investigation into the toxic mechanisms, involving TO-induced remaining DNA damage, cell cycle arrest, and the synergistic effect of autophagy flow disruption. It provides new insights into the clinical applications of MT and TO.
TO was prepared at 50, 100, and 200 μM for a 48 h treatment of HepG2 cells, while zebrafish were administered at 50, 75, and 100 μM for 72 h. Transcriptomics and computational molecular simulations, including network pharmacology, molecular docking, and molecular dynamics simulation, were used for target prediction. Fluorescent probes, flow cytometry, quantitative real-time polymerase chain reaction, and western blotting were employed for mechanism verification.
TO disrupted the balance between reactive oxygen species and cellular antioxidant defense, resulting in mitochondrial damage and repression of DNA-dependent protein kinase catalytic subunit. This led to the inability to repair DNA damage and caused cell cycle arrest in the G1/S phase. As shown in computational molecular simulations and transcriptomics analysis, the repression of damaged organelle removal through autophagy flow disruption resulted in excessive injury and hepatocyte death.
By impairing DNA damage responses (DDRs) and autophagy, TO causes unrepaired DNA damage, which disrupts cell cycle progression through complex interactions with cyclin proteins and tumour suppressor genes, ultimately contributing to hepatotoxicity.
Genes / Markers
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Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping