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Updated: Mar 30, 2026

Acute Kidney Injury Model Induced by Cisplatin in Adult Zebrafish
Published on: May 15, 2021
DNA damage response in cisplatin-induced nephrotoxicity
Shiyao Zhu1, Navjotsingh Pabla2, Chengyuan Tang1
1Department of Nephrology, The Second Xiangya Hospital, Central South University, Changsha, Hunan, China.
Cisplatin chemotherapy causes kidney damage by inducing DNA damage and the DNA damage response (DDR) in renal cells. Modulating this DDR pathway may offer new ways to protect kidneys during cancer treatment.
Area of Science:
- Oncology
- Nephrology
- Molecular Biology
Background:
- Cisplatin is a vital chemotherapy agent but causes severe side effects, including acute kidney injury (AKI).
- Cisplatin-induced AKI is linked to damage in renal tubular cells.
- The DNA damage response (DDR) is increasingly recognized as a key factor in cisplatin nephrotoxicity.
Purpose of the Study:
- To explore the role of DNA damage and DDR in cisplatin-induced AKI.
- To identify potential therapeutic targets for preventing cisplatin nephrotoxicity.
Main Methods:
- Review of recent studies on cisplatin nephrotoxicity and DDR.
- Analysis of the mechanisms linking DNA damage to renal cell injury and death.
Main Results:
- Cisplatin accumulation in renal tubular cells triggers DNA damage.
- Activation of DDR pathways can lead to cell cycle arrest, DNA repair, or cell death.
- DDR plays a critical role in the pathogenesis of cisplatin-induced AKI.
Conclusions:
- DNA damage and DDR are central to cisplatin nephrotoxicity.
- Targeting DDR pathways presents a promising strategy for renoprotection in cancer patients.
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