Optimized Bionic Drug-Delivery-Inducing Immunogenic Cell Death and cGAS-STING Pathway Activation for Enhanced Photodynamic-Chemotherapy-Driven Immunotherapy in Prostate Cancer

Immunogenic cell death Sting
DOI: 10.1021/acsami.4c07072 Publication Date: 2024-08-09T11:35:06Z
ABSTRACT
Prostate cancer presents as a challenging disease, it is often characterized an immunologically "cold" tumor, leading to suboptimal outcomes with current immunotherapeutic approaches in clinical settings. Photodynamic therapy (PDT) harnesses reactive oxygen species generated by photosensitizers (PSs) disrupt the intracellular redox equilibrium. This process induces DNA damage both mitochondria and nucleus, activating of immunogenic cell death (ICD) cGAS-STING pathway. Ultimately, this cascade events leads initiation antitumor immune responses. Nevertheless, existing PSs face challenges, including tumor targeting, aggregation-induced quenching, insufficient levels regions. To end, versatile bionic nanoplatform has been designed for simultaneous delivery emission PS TPAQ-Py-PF
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