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用于癌症免疫治疗的二价金纳米团簇的射频激活细胞焦亡

Radiofrequency-Activated Pyroptosis of Bi-Valent Gold Nanocluster for Cancer Immunotherapy.

作者信息

Zhang Qingqing, Shi Dingwen, Guo Mengqin, Zhao Hao, Zhao Yanbing, Yang Xiangliang

机构信息

National Engineering Research Center for Nanomedicine, Key Laboratory of Molecular Biophysics of Ministry of Education, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan430074, People's Republic of China.

Hubei Key Laboratory of Bioinorganic Chemistry and Materia Medica, Hubei Engineering Research Center for Biomaterials and Medical Protective Materials, Huazhong University of Science and Technology, Wuhan430074, People's Republic of China.

出版信息

ACS Nano. 2023 Jan 10;17(1):515-529. doi: 10.1021/acsnano.2c09242. Epub 2022 Dec 29.


DOI:10.1021/acsnano.2c09242
PMID:36580577
Abstract

Pyroptosis is gasdermin-mediated programmed necrosis that exhibits promising potential application in cancer immunotherapy, and the main challenge lies in how to provoke specific pyroptosis of tumor cells. Here, GC@PNA with a precisely stoichiometric ratio of Au(I) ion/Au(0) atom induced pyroptosis of tumor cells by its radiofrequency (RF)-heating effect. An / assay on 4T1 tumor cells indicates RF-activated pyroptosis of tumor cells elicits a robust ICD effect, enhancing the synergistic antitumor efficacy of GC@PNA with decitabine, significantly suppressing tumor metastasis and relapse by provoking systemic antitumor immune responses. Utilizing RF-activated pyroptotic immune responses, GC@PNA efficiently enhances the antitumor efficacy of αPD-1 immunotherapy under RF irradiation and provides a promising strategy for improving cancer immunotherapy by the noninvasive RF field with high clinical transformation potential.

摘要

细胞焦亡是由gasdermin介导的程序性坏死,在癌症免疫治疗中具有广阔的潜在应用前景,而主要挑战在于如何引发肿瘤细胞的特异性焦亡。在此,具有精确化学计量比的金(I)离子/金(0)原子的GC@PNA通过其射频(RF)加热效应诱导肿瘤细胞焦亡。对4T1肿瘤细胞的一项分析表明,射频激活的肿瘤细胞焦亡引发了强大的免疫原性细胞死亡(ICD)效应,增强了GC@PNA与地西他滨的协同抗肿瘤疗效,通过激发全身抗肿瘤免疫反应显著抑制肿瘤转移和复发。利用射频激活的焦亡免疫反应,GC@PNA在射频照射下有效增强了αPD-1免疫治疗的抗肿瘤疗效,并为通过具有高临床转化潜力的非侵入性射频场改善癌症免疫治疗提供了一种有前景的策略。

相似文献

[1]
Radiofrequency-Activated Pyroptosis of Bi-Valent Gold Nanocluster for Cancer Immunotherapy.

ACS Nano. 2023-1-10

[2]
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Adv Mater. 2023-6

[3]
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[4]
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J Mater Chem B. 2024-4-24

[5]
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ACS Nano. 2024-3-5

[6]
An acid-responsive MOF nanomedicine for augmented anti-tumor immunotherapy via a metal ion interference-mediated pyroptotic pathway.

Biomaterials. 2023-11

[7]
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J Control Release. 2024-9

[8]
Sonodynamic-immunomodulatory nanostimulators activate pyroptosis and remodel tumor microenvironment for enhanced tumor immunotherapy.

Theranostics. 2023

[9]
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Biomater Sci. 2023-3-14

[10]
Programming cell pyroptosis with biomimetic nanoparticles for solid tumor immunotherapy.

Biomaterials. 2020-9

引用本文的文献

[1]
A pyroptosis proportion tunable nano-modulator for cancer immunotherapy.

Theranostics. 2025-7-25

[2]
BioGoldNCDB: A Database of Gold Nanoclusters and Related Nanoparticles with Biomedical Activity.

Molecules. 2025-8-7

[3]
Multifunctional nanoagent for enhanced cancer radioimmunotherapy via pyroptosis and cGAS-STING activation.

J Nanobiotechnology. 2025-7-21

[4]
Zinc ions trigger PANoptosis-like cell death in magnetic hyperthermia therapy of magnesium based implant for hepatocellular carcinoma.

Apoptosis. 2025-6-19

[5]
Nanomaterials evoke pyroptosis boosting cancer immunotherapy.

Acta Pharm Sin B. 2025-2

[6]
Targeting pyroptosis reverses KIAA1199-mediated immunotherapy resistance in colorectal cancer.

J Immunother Cancer. 2025-2-25

[7]
Emerging strategies for nitric oxide production and their topical application as nanodressings to promote diabetic wound healing.

J Nanobiotechnology. 2025-1-29

[8]
Platinum nanoparticles in cancer therapy: chemotherapeutic enhancement and ROS generation.

Med Oncol. 2025-1-9

[9]
Nanomaterials Enhance Pyroptosis-Based Tumor Immunotherapy.

Int J Nanomedicine. 2024

[10]
Advancements in Stimulus-Responsive Co-Delivery Nanocarriers for Enhanced Cancer Immunotherapy.

Int J Nanomedicine. 2024-4-8

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