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Updated: Jul 14, 2026

A Doxorubicin-induced Cardiomyopathy Model in Adult Zebrafish
Published on: June 7, 2018
Doxorubicin induces a reversible senescence-like state in the EPC fish cell line
Keonhee Lee1, Kunihiko Futami1
1Department of Marine Biosciences, Tokyo University of Marine Science and Technology, Konan 4-5-7, Minato, Tokyo, 108-8477, Japan.
Abstract:
Cellular senescence is generally defined as a stable and typically irreversible cell cycle arrest triggered by diverse stresses, including DNA damage. However, fish-derived cells exhibit intrinsic resistance to stable senescence, and the extent to which this resistance can be overcome remains unclear. Here, we studied the effects of the DNA-damaging chemotherapeutic agent doxorubicin (DOX) in the fish cell line Epithelioma papulosum cyprini (EPC). DOX treatment induced multiple senescence-associated phenotypes in EPC cells, including morphological changes, senescence-associated β-galactosidase (SA-β-gal) activity, and the secretion of senescence-associated secretory phenotype (SASP) factors. Despite these changes, EPC cells did not undergo irreversible proliferative arrest and were able to resume proliferation in a condition-dependent manner, even after prolonged DOX exposure. Furthermore, these responses in EPC cells were not stably maintained but instead exhibited dynamic regulation across phenotypic, proliferative, and transcriptional states. Together, these findings demonstrate that DOX-induced DNA damage results in a transient and reversible senescence-like state in EPC cells, highlighting fundamental differences between teleost and mammalian senescence programs.
Insights
Fish cells show resistance to permanent cell cycle arrest, exhibiting a temporary senescence-like state after DNA damage. This highlights key differences between fish and mammalian senescence responses.
Area of Science:
- Cell Biology
- Comparative Biology
Background:
- Cellular senescence is a stable, irreversible cell cycle arrest triggered by stress, crucial in mammals.
- Fish cells display inherent resistance to stable senescence, with limited understanding of its modulation.
Purpose of the Study:
- To investigate the effects of doxorubicin (DOX), a DNA-damaging agent, on senescence in the fish cell line Epithelioma papulosum cyprini (EPC).
- To determine if fish cells can undergo stable senescence or if their response is transient and reversible.
Main Methods:
- EPC cells were treated with doxorubicin (DOX).
- Assessed for senescence-associated phenotypes: morphological changes, SA-β-gal activity, and SASP factor secretion.
- Monitored cell proliferation and transcriptional states post-treatment.
Main Results:
- DOX induced senescence-associated phenotypes in EPC cells, including SA-β-gal activity and SASP factor secretion.
- Despite these markers, EPC cells did not achieve irreversible cell cycle arrest and could resume proliferation.
- Senescence responses were dynamic and not stably maintained, indicating reversibility.
Conclusions:
- Doxorubicin-induced DNA damage triggers a transient and reversible senescence-like state in EPC cells, not a stable arrest.
- These findings underscore fundamental distinctions between teleost (fish) and mammalian senescence pathways.
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