Biomaterials, Journal Year: 2024, Volume and Issue: 316, P. 123027 - 123027
Published: Dec. 15, 2024
Language: Английский
Biomaterials, Journal Year: 2024, Volume and Issue: 316, P. 123027 - 123027
Published: Dec. 15, 2024
Language: Английский
ACS Nano, Journal Year: 2025, Volume and Issue: 19(1), P. 488 - 503
Published: Jan. 4, 2025
The concept of immunogenic cell death (ICD) induced by chemotherapy as a potential synergistic modality for cancer immunotherapy has been widely discussed. Unfortunately, most chemotherapeutic agents failed to dictate effective ICD responses due their defects in inducing potent signaling. Here, we report dual-enzyme-instructed peptide self-assembly platform CPMC (CPT-GFFpY-PLGVRK-Caps) that cooperatively utilizes camptothecin (CPT) and capsaicin (Caps) promote engage systemic adaptive immunity tumor rejection. Although CPT Caps respectively prevent progression inhibiting type-I DNA topoisomerase activating transient receptor cation channel subfamily V member 1 (TRPV1) intracellular calcium overload, neither alone effectively stimulates sufficient signaling meet immunotherapeutic needs. CPMC, sequentially allowing an active derivative VRK-Caps release extracellularly intracellularly, can synergize two distinct apoptosis pathways stimulated increase immunogenicity elicit T-cell-based immunity. Consequently, facilitates the generation improved tumor-specific cytotoxic T-cell sustained immunological memory, successfully suppressing both primary distant tumors. Moreover, render tumors susceptible PD-L1 blockade with antiprogrammed death-ligand (aPDL1) antibody inhibition. Combining drugs low ICD-stimulating capacity using strategy was demonstrated boost potentiate immunotherapy.
Language: Английский
Citations
1International Journal of Biological Macromolecules, Journal Year: 2025, Volume and Issue: 299, P. 140116 - 140116
Published: Jan. 20, 2025
Language: Английский
Citations
0Journal of Colloid and Interface Science, Journal Year: 2025, Volume and Issue: 688, P. 688 - 702
Published: Feb. 27, 2025
Language: Английский
Citations
0Journal of Colloid and Interface Science, Journal Year: 2025, Volume and Issue: 690, P. 137332 - 137332
Published: March 14, 2025
Language: Английский
Citations
0Advanced Healthcare Materials, Journal Year: 2024, Volume and Issue: 13(20)
Published: May 5, 2024
Abstract Phototherapy promotes anti‐tumor immunity by inducing immunogenic cell death (ICD), However, the accompanying inflammatory responses also trigger immunosuppression, attenuating efficacy of photo‐immunotherapy. Herein, they co‐assembled a cell‐membrane targeting chimeric peptide C16‐Cypate‐RRKK‐PEG 8 ‐COOH (CCP) and anti‐inflammatory diclofenac (DA) to develop nanodrug (CCP@DA) that both enhances immune effect phototherapy weakens inflammation‐mediated immunosuppression. CCP@DA achieves membrane‐targeting photodynamic photothermal synergistic therapies damage programmed ligand 1 (PD‐L1) induce strong ICD activate response. Simultaneously, released DA inhibits cycoperoxidase‐2 (COX‐2)/prostaglandin E2 (PGE 2 ) pathway in tumor cells inhibit pro‐tumor inflammation further down‐regulate PD‐L1 expression relieve immunosuppressive microenvironment. significantly inhibited growth vitro vivo, while maintaining potent Additionally, it exhibits excellent anti‐metastatic capabilities prolongs mouse survival time with single dose low levels near‐infrared (NIR) light exposure. This work provides valuable strategy control therapy‐induced for high‐efficiency photoimmunotherapy.
Language: Английский
Citations
3ACS Applied Materials & Interfaces, Journal Year: 2024, Volume and Issue: 16(33), P. 43364 - 43373
Published: Aug. 6, 2024
Calcium-overload-mediated tumor therapy has received considerable interest in oncology. However, its efficacy been proven to be inadequate due insufficient calcium ion concentration at the site coupled with challenges facilitating efficient uptake by tumors, leading unsatisfactory therapeutic outcomes. In present study, carbonate nanoshell mineralized ferric polydopamine nanoparticles (Fe-PDA@CaCO
Language: Английский
Citations
2Journal of Colloid and Interface Science, Journal Year: 2024, Volume and Issue: 678, P. 897 - 912
Published: Sept. 20, 2024
Language: Английский
Citations
2Acta Pharmaceutica Sinica B, Journal Year: 2024, Volume and Issue: 14(12), P. 5407 - 5417
Published: Sept. 21, 2024
Tumor microenvironment activatable therapeutic agents and their effective tumor accumulation are significant for selective treatment. Herein, we provide an unadulterated nanomaterial combining the above advantages. We synthesize a perylene diimide (PDI) molecule substituted by glutamic acid (Glu), which can self-assemble into small spherical nanoparticles (PDI-SG) in aqueous solution. PDI-SG not only be transformed nanofibers at low pH conditions but also reduced to PDI radical anion (PDI·‒), exhibits strong near-infrared absorption excellent photothermal performance. More importantly, PDI·‒ hypoxic tumors ablate minimize damage normal tissues. The morphological transformation from makes better retention. This work sheds light on design of therapeutics with precise structures high-performance therapy.
Language: Английский
Citations
1International Journal of Biological Macromolecules, Journal Year: 2024, Volume and Issue: 282, P. 137192 - 137192
Published: Nov. 1, 2024
Language: Английский
Citations
1Chemical Engineering Journal, Journal Year: 2024, Volume and Issue: 501, P. 157747 - 157747
Published: Nov. 17, 2024
Language: Английский
Citations
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