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一种用于增强肿瘤清除和联合免疫治疗的氧化应激纳米放大器

An Oxidative Stress Nano-Amplifier for Improved Tumor Elimination and Combined Immunotherapy.

作者信息

Zhang Wei, Ran Yijun, Yang Mi, Hu Yaqin, Wang Zhigang, Cao Yang, Ran Haitao

机构信息

Department of Ultrasound, Second Affiliated Hospital of Chongqing Medical University & Chongqing Key Laboratory of Ultrasound Molecular Imaging, Chongqing, 400010, China.

Department of Radiology, Second Affiliated Hospital of Chongqing Medical University, Chongqing, 400010, China.

出版信息

Adv Healthc Mater. 2024 Dec;13(31):e2402349. doi: 10.1002/adhm.202402349. Epub 2024 Sep 2.

DOI:10.1002/adhm.202402349
PMID:39221686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11650535/
Abstract

Amplifying oxidative stress to disrupt intracellular redox homeostasis can accelerate tumor cell death. In this work, an oxidative stress amplifier (PP@T) is prepared for enhanced tumor oxidation therapy to reduce tumor growth and metastases. The nano-amplifier has been successfully constructed by embedding MTH1 inhibitor (TH588) in the PDA-coated porphyrin metal-organic framework PCN-224. The controllable-released TH588 is demonstrated from pores can hinder MTH1-mediated damage-repairing process by preventing the hydrolysis of 8-oxo-dG, thereby amplifying oxidative stress and exacerbating the oxidative DNA damage induced by the sonodynamic therapy of PP@T under ultrasound irradiation. Furthermore, PP@T can effectively induce immunogenic cell death to trigger systemic anti-tumor immune response. When administered in combination with immune checkpoint blockade, PP@T not only impedes the progression of the primary tumor but also achieves obvious antimetastasis in breast cancer murine models, including orthotopic and artificial whole-body metastasis models. Furthermore, the nanoplatform also provides photoacoustic imaging for in vivo treatment guidance. In conclusion, by amplifying oxidative stress and reactive oxygen species sensitized immunotherapy, this image-guided nanosystem shows potential for highly specific, effective combined therapy against tumor cells with negligible side-effects to normal cells which will provide a new insight for precise tumor treatment.

摘要

增强氧化应激以破坏细胞内氧化还原稳态可加速肿瘤细胞死亡。在这项工作中,制备了一种氧化应激放大器(PP@T)用于增强肿瘤氧化治疗,以减少肿瘤生长和转移。通过将MTH1抑制剂(TH588)嵌入聚多巴胺包覆的卟啉金属有机框架PCN - 224中,成功构建了这种纳米放大器。从孔中释放的可控TH588可通过阻止8 - 氧代脱氧鸟苷的水解来阻碍MTH1介导的损伤修复过程,从而增强氧化应激并加剧PP@T在超声照射下的声动力疗法诱导的氧化性DNA损伤。此外,PP@T可有效诱导免疫原性细胞死亡以触发全身抗肿瘤免疫反应。当与免疫检查点阻断联合使用时,PP@T不仅能阻碍原发性肿瘤的进展,还能在乳腺癌小鼠模型(包括原位和人工全身转移模型)中实现明显的抗转移作用。此外,该纳米平台还提供光声成像用于体内治疗指导。总之,通过增强氧化应激和活性氧致敏免疫疗法,这种图像引导的纳米系统显示出对肿瘤细胞进行高度特异性、有效联合治疗的潜力,对正常细胞的副作用可忽略不计,这将为精确肿瘤治疗提供新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f1/11650535/c816df496180/ADHM-13-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f1/11650535/eabeee13a657/ADHM-13-0-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f1/11650535/27e5b92f2228/ADHM-13-0-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f1/11650535/6544b0de4d42/ADHM-13-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f1/11650535/46b854f19f64/ADHM-13-0-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f1/11650535/ed8cb070fd5d/ADHM-13-0-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f1/11650535/5b633ac1e505/ADHM-13-0-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f1/11650535/c816df496180/ADHM-13-0-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f1/11650535/eabeee13a657/ADHM-13-0-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f1/11650535/27e5b92f2228/ADHM-13-0-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f1/11650535/6544b0de4d42/ADHM-13-0-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f1/11650535/46b854f19f64/ADHM-13-0-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f1/11650535/ed8cb070fd5d/ADHM-13-0-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f1/11650535/5b633ac1e505/ADHM-13-0-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63f1/11650535/c816df496180/ADHM-13-0-g001.jpg

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