Excessive autophagy-inducing and highly penetrable biomineralized bacteria for multimodal imaging-guided and mild hyperthermia-enhanced immunogenic cell death.

J Colloid Interface Sci

School of Biomedical Engineering, State Key Laboratory of Marine Resource Utilization in the South China Sea, Hainan University, Haikou 570228, China; School of Life and Health Sciences, Key Laboratory of Biomedical Engineering of Hainan Province, Collaborative Innovation Center of One Health, Hainan University, Haikou 570228, China. Electronic address:

Published: February 2025

AI Article Synopsis

  • The tumor microenvironment is hypoxic and can boost the effectiveness of anaerobic bacteria like S. typhimurium in treating cancer, though their long-term efficacy is limited and often leads to tumor regrowth.
  • To enhance treatment, a new biohybrid system called S@UIL was created, which combines S. typhimurium with a zirconium-based framework loaded with ICG and luteolin, improving tumor targeting and therapy through autophagy and mild hyperthermia.
  • In tests on colon cancer, this system promotes cell death and immune activation, making it a promising single-treatment option that may reduce tumor immune evasion and improve cancer management.

Article Abstract

The tumor microenvironment, characterized by hypoxia, supports the efficacy of anaerobic bacteria like attenuated S. typhimurium in cancer therapies. These bacteria target and penetrate deep tumor regions, significantly reducing tumor size but often lead to tumor regrowth due to limited long-term efficacy. To enhance the therapeutic impact, a novel biohybrid system, S@UIL, has been developed by coating S. typhimurium with a zirconium-based nanoscale metal-organic framework (UiO-66-NH) loaded with indocyanine green (ICG) and luteolin (LUT). This system maintains the bacteria's tumor-targeting ability while increasing the penetration and therapeutic effectiveness through excessive autophagy and mild hyperthermia. In a subcutaneous colon cancer model, the integration of LUT and ICG promotes autophagic cell death and photothermal sensitization, leading to the release of damage-associated molecular patterns (DAMPs). These DAMPs activate immune responses through dendritic cells and T-cells, enhancing immunogenic cell death (ICD) and potentially reducing immune evasion by tumors. This single-administration approach also integrates multimodal imaging capabilities, providing a promising strategy for improved tumor ICD induction and cancer progression inhibition.

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Source
http://dx.doi.org/10.1016/j.jcis.2024.09.246DOI Listing

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