Combination therapy using microwave ablation and d-mannose-chelated iron oxide nanoparticles inhibits hepatocellular carcinoma progression

Microwave ablation Macrophage polarization Iron oxide nanoparticles Tumor progression
DOI: 10.1016/j.apsb.2022.05.026 Publication Date: 2022-05-29T13:53:10Z
ABSTRACT
Despite being a common therapy for hepatocellular carcinoma (HCC), insufficient thermal ablation can leave behind tumor residues that cause recurrence. This is believed to augment M2 inflammatory macrophages usually play pro-tumorigenic role. To address this problem, we designed d-mannose-chelated iron oxide nanoparticles (man-IONPs) polarize M2-like into the antitumor M1 phenotype. In vitro and in vivo experiments demonstrated man-IONPs specifically targeted accumulated peri-ablation zones after macrophage infiltration was augmented under microwave (MWA). The simultaneously induced polarization of phenotypes, enabling transformation immunosuppressive microenvironment an immunoactivating one. Post-MWA exerted robust inhibitory effects on HCC progression well-established orthotopic liver cancer mouse model. Thus, combining with salvage residual tumors MWA. These results have strong potential clinical translation.
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