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Updated: Apr 6, 2026

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Cell Death Associated with Abnormal Mitosis Observed by Confocal Imaging in Live Cancer Cells
Published on: August 21, 2013
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Mitotic abnormality induced by evodiamine, a tryptamine indole alkaloid
Ryoya Shigefuji1, Seiji Komatsu1, Takeshi Terabayashi2
1Department of Advanced Medical Sciences, Oita University, Yufu, Oita 879-5503, Japan.
Toxicology and Applied Pharmacology
|April 5, 2026
Summary
Evodiamine, a compound from herbal medicine, shows promise as an anticancer drug candidate. It selectively kills proliferating cells by disrupting chromosome segregation during mitosis.
Area of Science:
- Pharmacology
- Cell Biology
- Oncology
Background:
- Mitotic inhibitors are crucial in cell biology research and cancer chemotherapy.
- East Asian herbal medicines are a potential source of novel anticancer agents.
Purpose of the Study:
- To identify and characterize new anticancer drug candidates from herbal medicines.
- To investigate the molecular mechanisms of evodiamine's cytotoxic effects.
Main Methods:
- Screening of herbal medicine compounds for cytotoxic activity.
- Comparative analysis of evodiamine and rutaecarpine effects on cell proliferation.
- Microscopic examination of chromosome segregation and mitotic progression in treated cells.
Main Results:
- Evodiamine exhibited selective cytotoxicity against proliferating cells, unlike structurally similar rutaecarpine.
- Evodiamine treatment led to premature chromatid distribution and micronucleus formation during mitosis.
- Higher concentrations of evodiamine induced prophase arrest, indicating mitotic disruption.
Conclusions:
- Evodiamine is a potential anticancer drug candidate with selective toxicity towards proliferating cells.
- The compound induces chromosomal segregation abnormalities, leading to cell death.
- Evodiamine's mechanism of action involves disrupting mitosis, making it a promising therapeutic agent.
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