Modulation of the Tumor Immune Microenvironment by Bi 2 Te 3 -Au/Pd-Based Theranostic Nanocatalysts Enables Efficient Cancer Therapy.
Fengxia WuHaoran ChenRuiqi LiuYongkuan SuoQiqing LiYoulin ZhangHongguang LiuZhen ChengYulei ChangPublished in: Advanced healthcare materials (2022)
Nanozymes with multienzyme-mimicking activities have shown great potential in cancer therapy due to their ability to modulate the complex tumor microenvironment (TME). Herein, a second near-infrared (NIR-II) photothermal-nanocatalyst by decorating Bi 2 Te 3 nanosheets with ultrasmall Au/Pd bimetallic nanoparticles (Bi 2 Te 3 -Au/Pd) to reverse the immunosuppressive TME is developed. The peroxidase (POD)-like and catalase (CAT)-like activities, and glutathione (GSH) consumption capacity of Au/Pd modulates the TME by disrupting the intracellular redox homeostasis and relieving hypoxia in the TME. Notably, the amplified oxidative stress induces the accumulation of lipid hydroperoxides (LPO) for enhanced ferroptosis. Moreover, upon NIR-II photoirradiation at 1064 nm, the localized heat generated by Bi 2 Te 3 not only directly ablates the cancer cells but also enhances the Au/Pd-mediated catalysis-mediated cancer therapy. Furthermore, both in vitro and in vivo studies confirm that the Bi 2 Te 3 -Au/Pd nanocatalysts (BAP NCs) can effectively suppress tumor growth by inducing immunogenic cell death (ICD), and suppressing metastasis and recurrence by the synergistic treatment. Overall, this study provides a promising theranostic strategy for effective tumor inhibition.
Keyphrases
- cancer therapy
- photodynamic therapy
- sensitive detection
- reduced graphene oxide
- drug delivery
- cell death
- oxidative stress
- fluorescence imaging
- visible light
- stem cells
- fluorescent probe
- quantum dots
- drug release
- gold nanoparticles
- signaling pathway
- fatty acid
- free survival
- heat stress
- risk assessment
- human health
- metal organic framework
- replacement therapy