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谷胱甘肽/ pH响应性铜基级联纳米复合物通过铜死亡/铁死亡/坏死性凋亡诱导口腔鳞状细胞癌发生免疫原性细胞死亡

GSH/pH-responsive copper-based cascade nanocomplexes inducing immunogenic cell death through cuproptosis/ferroptosis/necroptosis in oral squamous cell carcinoma.

作者信息

Sun Yi, Li Enze, Zhong Wenzhao, Deng Zhaoming, Zhou Ziyao, Wong Ka Hong, Li Xiangwei

机构信息

Stomatology Department, The Fifth Affiliated Hospital, Sun Yat-sen University, Zhuhai, Guangdong, China.

State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macau.

出版信息

Mater Today Bio. 2024 Dec 28;30:101434. doi: 10.1016/j.mtbio.2024.101434. eCollection 2025 Feb.

Abstract

Oral squamous cell carcinoma (OSCC) remains a formidable challenge due to high recurrence rates and limited efficacy of conventional treatments. Immunotherapy holds potential, but its effectiveness is often restricted by low patient responsiveness. This study presents a novel therapeutic strategy using GSH/pH-responsive copper-based cascade nanocomplexes to induce immunogenic cell death (ICD) in OSCC. The fabricated nanocomplex, PC@B-H, leverages the acidic and reducing tumor microenvironment to release copper ions and plumbagin, triggering a cascade of cell death mechanisms including cuproptosis, ferroptosis, and necroptosis. This multifunctional system not only enhances oxidative stress but also depletes glutathione, promotes lipid peroxidation, and disrupts mitochondrial function, leading to robust tumor inhibition. Additionally, the induction of ICD facilitates dendritic cell maturation and cytotoxic T lymphocyte infiltration, providing durable anti-tumor immunity. The study demonstrates that PC@B-H achieves a 92.3 % tumor growth inhibition rate with minimal systemic toxicity, offering a promising avenue for enhancing the efficacy of OSCC treatment through combined cell death pathways and immune activation.

摘要

由于高复发率和传统治疗方法疗效有限,口腔鳞状细胞癌(OSCC)仍然是一个严峻的挑战。免疫疗法具有潜力,但其有效性常常受到患者低反应性的限制。本研究提出了一种使用谷胱甘肽/ pH响应性铜基级联纳米复合物在OSCC中诱导免疫原性细胞死亡(ICD)的新型治疗策略。制备的纳米复合物PC@B-H利用酸性和还原性肿瘤微环境释放铜离子和白花丹醌,引发包括铜死亡、铁死亡和坏死性凋亡在内的一系列细胞死亡机制。这种多功能系统不仅增强氧化应激,还消耗谷胱甘肽,促进脂质过氧化,并破坏线粒体功能,从而实现强大的肿瘤抑制作用。此外,ICD的诱导促进树突状细胞成熟和细胞毒性T淋巴细胞浸润,提供持久的抗肿瘤免疫力。该研究表明,PC@B-H实现了92.3%的肿瘤生长抑制率,且全身毒性最小,为通过联合细胞死亡途径和免疫激活提高OSCC治疗效果提供了一条有前景的途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b02/11750277/930a84fa5d2d/ga1.jpg

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