Iteratively Designed Nanocarrier for Cell Cycle Arrest, Immune Boost, and T Cell Access
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Abstract
Abstract Recent advancements in cancer therapy have highlighted the dual role of cyclin-dependent kinase 4/6 inhibitors (CDK4/6i) in both cell cycle regulation and immune activation. However, applying CDK4/6i to immunologically unfavorable tumors is challenging due to the complex tumor microenvironment (TME), characterized by inadequate T cell recruitment and exclusion mechanisms that hinder an effective anti-tumor immunity. Here, we iteratively designed prodrug liposomal nanocarriers that integrate multiple functions: cell cycle inhibition through CDK4/6i encapsulation, immune activation via concurrent delivery of an immunogenic cell death-inducing chemotherapy agent, and overcoming T cell exclusion through the incorporation of a cholesterol prodrug. This iterative nanocarrier design effectively improves the pharmacokinetic profile of CDK4/6i, overcomes the immunosuppressive TME, achieves superior anti-tumor efficacy, and synergizes with immune checkpoint inhibitors to provide lasting effects in various colon cancer animal models.
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- europepmc
- last seen: 2026-05-20T01:45:00.602351+00:00