1. Department of Medical Oncology, The First Affiliated Hospital of Xi’an Jiaotong University, Xi’an 710061, PR. China;
2. Institute for Stem Cell & Regenerative Medicine, The Second Affiliated Hospital of Xi’an Jiaotong University, Xi’an 710004, PR. China;
3. Department of Oncology, Shaanxi Provincial People’s Hospital, Xi’an 710068, PR. China;
4. Engineering Research Center of Tropical Medicine Innovation and Transformation of Ministry of Education, Hainan Medical University, Haikou 571199, China;
5. School of Pharmacy, Xi'an Jiaotong University, Xi'an 710061, PR. China;
6. Department of Tumor and Immunology in Precision Medical Institute, The Second Affiliated Hospital of Xi’an Jiaotong University, Xi'an 710004, PR. China;
7. College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, PR. China;
8. Department of Hepatology, The Second Affiliated Hospital of Xi’an Jiaotong University, Xi'an 710004, PR. China
Funds:
This work was supported by the National Natural Science Foundation of China (Grant number: 82203051), the Natural Science Basic Research Plan in Shaanxi Province of China (Grant number: 2023-JC-QN-0815), the Elite talent program of Shaanxi Provincial People's Hospital (Grant number: 2022JY-43), and the Beijing Xisike Clinical Oncology Research Foundation (Grant number: Y-HH202101-0234). We would like to sincerely appreciate the Instrument Analysis Center of Xi’an Jiaotong University for their assistance with TEM, FT-IR, and DLS analysis, and senior engineer Lai Baochang of Xi’an Jiaotong University for providing the technical support of CLSM.
Microsatellite-stable colorectal cancer (MSS-CRC) is characterized by poor immune infiltration and immune evasion, leading to rapid tumor progression and limited efficacy of current immunotherapies. The bioinformatics analysis revealed that the hyperactivation of the Wnt/β-catenin signaling pathway in MSS-CRC is instrumental in mediating immune suppression. Although inhibiting this pathway presents a therapeutic opportunity, no Wnt inhibitors have been clinically approved due to Wnt's essential role in maintaining tissue homeostasis, with inhibition in normal cells causing significant toxicity. To address it, we discovered that Wnt activation in colorectal cancer cells enhances macropinocytosis, particularly favoring the uptake of glycosylated proteins to meet increased nutrient demands. Building on this insight, we developed a glycosylated human serum albumin (GHSA) co-assembled with carnosic acid (CA), termed glycosylated human serum albumin-carnosic acid (GHSACA), which is selectively internalized by Wnt-activated colorectal cancer cells. This approach not only reduces off-target toxicity but also effectively inhibits the Wnt pathway, resulting in notable tumor inhibition and immune reactivation in murine models, while maintaining a favorable safety profile. This strategy offers a promising therapeutic solution by combining selective Wnt inhibition with enhanced immune activation in MSS-CRC, and highlights the potential of leveraging disease-specific cellular uptake mechanisms for designing nanomedicines, advancing the development of precision-targeted cancer therapies.