宝藿苷Ⅰ与索拉非尼的药物组合物及其在制备抗肝癌药物中的应用

By combining cyproheptadine I with sorafenib, the Ras/MAPK pathway is synergistically inhibited and metabolic reprogramming is induced, thus solving the problems of drug resistance and adverse reactions of sorafenib in the treatment of hepatocellular carcinoma and achieving a more effective treatment effect for liver cancer.

CN122398835APending Publication Date: 2026-07-17CHENZHOU NO 1 PEOPLES HOSPITAL

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
CHENZHOU NO 1 PEOPLES HOSPITAL
Filing Date
2026-05-25
Publication Date
2026-07-17

AI Technical Summary

Technical Problem

Sorafenib's efficacy in treating hepatocellular carcinoma (HCC) is limited by drug resistance and adverse reactions, and existing studies have not explored the mechanism of combination therapy between cyproheptadine I and sorafenib.

Method used

A pharmaceutical composition of cyproheptadine I and sorafenib was provided. Through high-throughput screening and multi-omics analysis, it was confirmed that the synergistic inhibition of the Ras/MAPK pathway and the induction of metabolic reprogramming were used to prepare an anti-liver cancer drug.

Benefits of technology

It significantly inhibits the proliferation, migration, and invasion of liver cancer cells, reverses the EMT process, reduces the toxic side effects of sorafenib, improves patient compliance, and provides a multi-target combination strategy to overcome drug resistance.

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Abstract

本发明公开了宝藿苷Ⅰ与索拉非尼的药物组合物及其在制备抗肝癌药物中的应用,属于医药技术领域。本发明通过高通量筛选发现,宝藿苷Ⅰ能与索拉非尼在多种肝癌细胞系中稳定产生协同效应的天然化合物。体内外实验证实,该组合物可显著抑制肝癌细胞增殖、迁移、侵袭及上皮‑间充质转化,并诱导细胞凋亡。机制研究表明,该组合物通过协同抑制Ras / MAPK信号通路及诱导代谢重编程发挥抗肿瘤作用。动物实验显示,该组合物能显著抑制肝癌异种移植瘤生长,且无明显毒性。本发明为克服索拉非尼耐药提供了新的联合治疗策略。
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