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Cinobufagin as a Potential Intervention Against Liver Cancer-A Comprehensive Review
Nicole Simone de Lima Coelho1, Victória Dogani Rodrigues1, Otávio Simões Girotto2
1Department of Biochemistry and Pharmacology, School of Medicine, Faculdade de Medicina de Marília (FAMEMA), Marília 17519-030, SP, Brazil.
Cinobufagin (CB), a compound from toad venom, shows promise for treating liver cancer by inducing cell death and disrupting tumor growth. Further research is needed to optimize its clinical use and safety.
Area of Science:
- Oncology
- Pharmacology
- Traditional Chinese Medicine
Background:
- Hepatocellular carcinoma (HCC) presents a significant global health burden with high recurrence rates.
- Existing therapies for liver cancer have limited efficacy, necessitating novel treatment strategies.
- Cinobufagin (CB), a bufadienolide from toad secretions, exhibits diverse antitumor properties.
Purpose of the Study:
- To comprehensively review the evidence on Cinobufagin (CB) and cinobufacini for liver cancer treatment.
- To assess the pharmacodynamic actions and preclinical efficacy of CB in HCC models.
- To identify potential therapeutic applications and challenges for CB in clinical settings.
Main Methods:
- Literature review of preclinical studies (in vitro and in vivo) on Cinobufagin and cinobufacini in liver cancer.
- Analysis of CB's molecular mechanisms, including apoptosis induction, DNA damage, and pathway modulation (PI3K/Akt/mTOR, Akt/ERK, AURKA-mTOR-eIF4E).
- Evaluation of CB's effects on tumor metabolism, oxidative stress, proliferation, and migration.
Main Results:
- CB demonstrates significant antitumor efficacy in preclinical liver cancer models.
- Pharmacodynamic actions include apoptosis induction, DNA damage, and inhibition of proliferation/migration.
- CB modulates critical oncogenic pathways and disrupts tumor metabolism, inducing oxidative stress.
Conclusions:
- Cinobufagin (CB) exhibits considerable therapeutic potential for hepatocellular carcinoma (HCC).
- Preclinical data support CB's efficacy, but toxicity concerns at higher doses require attention.
- Further translational research is essential to optimize CB's clinical application, dosage, and safety profile for HCC treatment.
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