Summary
Pancreatic cancer is a highly malignant tumor with early metastasis, poor prognosis, and resistant to existing chemotherapy drugs such as oxaliplatin (Oxp). Therefore, a nanodrug of amorphous iron oxide packaged Oxp (AIOoxp) was proposed to achieve a more efficient treatment of orthotopic pancreatic cancer than that of free Oxp. The obtained AIOoxp increased the accumulation of Pt at tumor sites and effectively reduced Oxp-induced systemic toxicity. In addition, the Fe2+/Fe3+ ions released by AIOoxp react with H2O2 through Fenton's reaction and produce a large amount of reactive oxygen species (ROS), which further induce ferroptosis, thus promoting Oxp-induced apoptosis and achieve synergistic tumor therapy. Furthermore, AIOoxp nanoplatforms can signifi-cantly reduce the levels of carbohydrate antigen 19-9 (CA19-9), which is the most important biomarker and promoter of pancreatic cancer, suggesting favorable therapeutic effects and prognosis. Overall, this study pro-vides new insights and solutions for the clinical treatment of pancreatic cancer.
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Institution1; 哈尔滨医科大学; 中国科学院