Colloids and Surfaces B Biointerfaces, Год журнала: 2024, Номер 244, С. 114137 - 114137
Опубликована: Авг. 5, 2024
Язык: Английский
Colloids and Surfaces B Biointerfaces, Год журнала: 2024, Номер 244, С. 114137 - 114137
Опубликована: Авг. 5, 2024
Язык: Английский
Journal of Controlled Release, Год журнала: 2024, Номер 371, С. 429 - 444
Опубликована: Июнь 8, 2024
Язык: Английский
Процитировано
10Journal of Nanobiotechnology, Год журнала: 2024, Номер 22(1)
Опубликована: Май 9, 2024
Abstract Radiotherapy-induced immune activation holds great promise for optimizing cancer treatment efficacy. Here, we describe a clinically used radiosensitizer hafnium oxide (HfO 2 ) that was core coated with MnO shell followed by glucose oxidase (GOx) doping nanoplatform @MnO @GOx, HMG) to trigger ferroptosis adjuvant effects glutathione depletion and reactive oxygen species production. This cascade potentiation further sensitized radiotherapy enhancing DNA damage in 4T1 breast tumor cells. The combination of HMG nanoparticles effectively activated the damaged Mn 2+ -mediated cGAS-STING pathway vitro vivo. process had significant inhibitory on progression initiating an anticancer systemic response prevent distant recurrence achieve long-lasting suppression both primary tumors. Furthermore, as-prepared “turned on” spectral computed tomography (CT)/magnetic resonance dual-modality imaging signals, demonstrated favorable contrast enhancement capabilities under GSH microenvironment. result highlighted potential as theranostic achieving molecular guided sensitization induced synergistic immunotherapy.
Язык: Английский
Процитировано
7Coordination Chemistry Reviews, Год журнала: 2024, Номер 517, С. 215969 - 215969
Опубликована: Июнь 10, 2024
Язык: Английский
Процитировано
7Advanced Healthcare Materials, Год журнала: 2024, Номер 13(30)
Опубликована: Авг. 13, 2024
Radio-immunotherapy driven by radiation-induced immunogenic cell death (ICD) is emerging as a potential opportunity to address conventional radiotherapy (RT) that only applicable localized tumor treatment. However, the effective activation of ICD during RT severely limited radiation dose, weak immunogenicity, and radio-resistance caused microenvironment (TME). Herein, novel bimetallic hybrid nanoscale coordination nanostimulator first proposed phosphate backbone doped with copper ions (Cu
Язык: Английский
Процитировано
5Advanced Healthcare Materials, Год журнала: 2024, Номер 13(14)
Опубликована: Фев. 23, 2024
Abstract Immunotherapy has emerged as an innovative strategy with the potential to improve outcomes in cancer patients. Recent evidence indicates that radiation‐induced DNA damage can activate cyclic‐GMP‐AMP synthase (cGAS)‐stimulator of interferon genes (STING) pathway enhance antitumor immune response. Even so, only a small fraction patients currently benefits from radioimmunotherapy due radioresistance and inadequate activation cGAS‐STING pathway. Herein, this work integrates hafnium oxide (HfO 2 ) nanoparticles (radiosensitizer) 7‐Ethyl‐10‐hydroxycamptothecin (SN38, chemotherapy drug, STING agonist) into polydopamine (PDA)‐coated core‐shell nanoplatform @PDA/Fe/SN38) achieve synergistic chemoradiotherapy immunotherapy. The co‐delivery HfO /SN38 greatly enhances radiotherapy efficacy by effectively activating pathway, which then triggers dendritic cells maturation CD8 + T recruitment. Consequently, growth both primary abscopal tumors tumor‐bearing mice is efficiently inhibited. Moreover, @PDA/Fe/SN38 complexes exhibit favorable magnetic resonance imaging (MRI)/photoacoustic (PA) bimodal molecular properties. In summary, these developed multifunctional have intensify realize simultaneous Radio/Chemo/Immunotherapy for clinical translation.
Язык: Английский
Процитировано
4ACS Nano, Год журнала: 2024, Номер 18(43), С. 29439 - 29456
Опубликована: Окт. 15, 2024
The stimulator of interferon genes (STING) pathway is crucial for tumor immunity, leading to the exploration STING agonists as potential immunotherapy adjuvants. However, their clinical application faces obstacles including poor pharmacokinetics, transient activation, and an immunosuppressive microenvironment (TME). Addressing these limitations, our study aims develop injectable silk fibroin hydrogel-based in situ vaccine. It incorporates a nanoscale agonist, immunogenic cell death (ICD) inducer, immunomodulator ensure controlled sustained release. cGAMP nanoparticles (cGAMPnps) with core–shell structure optimal delivery dendritic cells (DCs), thereby activating fostering DC maturation. ICD-associated damage-associated molecular patterns amplify prolong activation via enhanced type I IFN other inflammatory pathways, along delayed degradation STING. Furthermore, STING-driven vascular normalization by cGAMPnps ICD, conjunction immunomodulators like antiprogrammed protein 1 antibody (anti-PD-1 Ab) or OX40 ligand (OX40L), effectively remodels TME. This gel vaccine, when used independently surgery neoadjuvant/adjuvant immunotherapy, enhances CD8+ T-cell suppressing progression recurrence across various immunologically cold models. revolutionizes cancer offering substantial promise improving outcomes broad spectrum malignancies.
Язык: Английский
Процитировано
4International Immunopharmacology, Год журнала: 2025, Номер 148, С. 114013 - 114013
Опубликована: Янв. 18, 2025
Язык: Английский
Процитировано
0Nano Today, Год журнала: 2025, Номер 61, С. 102656 - 102656
Опубликована: Фев. 5, 2025
Язык: Английский
Процитировано
0Journal of Controlled Release, Год журнала: 2025, Номер unknown
Опубликована: Фев. 1, 2025
Язык: Английский
Процитировано
0Advanced Healthcare Materials, Год журнала: 2025, Номер unknown
Опубликована: Март 3, 2025
Abstract The efficacy of radiotherapy is often limited by insufficient radiosensitization and tumor radioresistance. This study reports a dual‐functional hafnium oxide nanoplatform that combines high‐Z with Bcl‐2 gene silencing for enhanced cancer radiotherapy. developed surface modification nanoparticles polyethyleneimine, enabling efficient siRNA delivery while maintaining inherent radiosensitizing properties. Comprehensive physicochemical characterization confirmed the successful stable complexation. Upon radiation exposure, reactive oxygen species generation DNA damage simultaneously delivering to suppress radioresistance mechanisms. In vitro studies revealed significant enhancement radiation‐induced cell death through synergistic effects silencing, evidenced increased γ‐H2AX expression apoptotic population. murine colon model, achieved remarkable growth inhibition (80%) when combined exhibiting favorable biocompatibility in major organs. Mechanistic effective downregulation tissues, validating this therapeutic approach. presents promising strategy improving outcomes simultaneous suppression radioresistance, potentially advancing field
Язык: Английский
Процитировано
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