Chemotherapy-Induced Liver Injury: Unveiling Emerging Mechanisms and Exploring Mitigation Strategies

Document Type : Review article

Authors

1 Department of Pharmacology & Toxicology, Faculty of Pharmacy, Egyptian Russian University, Cairo 11829, Egypt

2 Pharmacology and Toxicology Department, Faculty of Pharmacy, Al-Azhar University, Cairo, Egypt.

Abstract

In this comprehensive overview of chemotherapy-induced liver injury, various classes of chemotherapeutic agents were reviewed to elucidate the complex cellular events contributing to hepatotoxicity and potential mitigation strategies. Alkylating agents, such as cyclophosphamide and busulfan, exhibited diverse mechanisms, with compounds like fucoidan and pyrroloquinoline quinone demonstrating protective effects through modulation of Nrf2/HO-1 and NF-κB pathways. Methotrexate-induced hepatotoxicity, characterized by oxidative stress and inflammation, highlighted the importance of addressing disruptions in lipid metabolism and the gut-liver axis. The multifaceted nature of cisplatin-induced liver damage emphasized the role of gastrointestinal microbiota and therapeutic interventions like curcumin. Anthracyclines, including doxorubicin and epirubicin, posed challenges in mitigating severe hepatotoxicity, with potential protective agents identified. Topoisomerase inhibitors, plant alkaloids, and antitumor antibodies showcased diverse impacts on liver function, emphasizing the need for tailored interventions. Targeted therapies, immune checkpoint inhibitors, and miscellaneous agents like L-asparaginase revealed distinct patterns of hepatotoxicity, prompting a nuanced understanding of patient safety. This comprehensive exploration offers a foundation for future research and therapeutic developments to enhance patient outcomes during chemotherapy.

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ERU Research Journal
Volume 3, Issue 4
October 2024
Pages 1540-1567

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