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负载PAD4抑制剂的层状双氢氧化物纳米片作为用于光动力疗法介导的肿瘤转移治疗的多功能纳米平台

PAD4 Inhibitor-Loaded Layered Double Hydroxide Nanosheets as a Multifunctional Nanoplatform for Photodynamic Therapy-Mediated Tumor Metastasis Treatment.

作者信息

Chen Rong, Hu Tingting, Lu Yu, Yang Shuqing, Zhang Min, Tan Chaoliang, Liang Ruizheng, Wang Yuji

机构信息

Department of Medicinal Chemistry, College of Pharmaceutical Sciences of Capital Medical University, Beijing, 100069, P. R. China.

Department Electrical and Electronic Engineering, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, 999077, P. R. China.

出版信息

Small. 2024 Dec;20(50):e2404211. doi: 10.1002/smll.202404211. Epub 2024 Oct 2.

Abstract

Photodynamic therapy (PDT) is demonstrated to be effective in inducing antitumor immune responses for tumor metastasis treatment. However, tumor hypoxia, inferior tissue penetration of light, and low singlet oxygen (O) quantum yield significantly hamper the efficacy of PDT, thus weakening its immune function. Moreover, PDT-mediated neutrophil extracellular traps (NETs) formation can further reduce the therapeutic effectiveness. Herein, the use of defect-rich CoMo-layered double hydroxide (DR-CoMo-LDH) nanosheets as a carrier to load a typical peptidyl arginine deiminase 4 inhibitor, i.e., YW4-03, to construct a multifunctional nanoagent (403@DR-LDH) for PDT/immunotherapy, is reported. Specifically, 403@DR-LDH inherits excellent O generation activity under 1550 nm laser irradiation and improves the half-life of YW4-03. Meanwhile, 403@DR-LDH plus 1550 nm laser irradiation can stimulate immunogenic cell death to promote the maturation of dendric cells and activation/infiltration of T cells and significantly downregulate H3cit protein expression to inhibit NETs formation, synergistically promoting the antitumor metastasis effect. Taken together, 403@DR-LDH can kill cancer cells and inhibit tumor growth/metastasis under 1550 nm laser irradiation. Single-cell analysis indicates that 403@DR-LDH can regulate the ratio of immune cells and immune-related proteins to improve the tumor immune microenvironment, showing strong efficacy to inhibit the tumor growth, metastasis, and recurrence.

摘要

光动力疗法(PDT)已被证明在诱导抗肿瘤免疫反应以治疗肿瘤转移方面是有效的。然而,肿瘤缺氧、光的组织穿透性差以及单线态氧(O)量子产率低显著阻碍了PDT的疗效,从而削弱了其免疫功能。此外,PDT介导的中性粒细胞胞外陷阱(NETs)形成会进一步降低治疗效果。在此,报道了使用富含缺陷的钴钼层状双氢氧化物(DR-CoMo-LDH)纳米片作为载体来负载一种典型的肽基精氨酸脱亚氨酶4抑制剂,即YW4-03,以构建用于PDT/免疫治疗的多功能纳米剂(403@DR-LDH)。具体而言,403@DR-LDH在1550 nm激光照射下继承了优异的产氧活性,并提高了YW4-03的半衰期。同时,403@DR-LDH加1550 nm激光照射可刺激免疫原性细胞死亡,促进树突状细胞成熟以及T细胞的激活/浸润,并显著下调H3cit蛋白表达以抑制NETs形成,协同促进抗肿瘤转移效果。综上所述,403@DR-LDH在1550 nm激光照射下可杀死癌细胞并抑制肿瘤生长/转移。单细胞分析表明,403@DR-LDH可调节免疫细胞和免疫相关蛋白的比例,改善肿瘤免疫微环境,显示出强大的抑制肿瘤生长、转移和复发的功效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9414/11636073/b72b45921727/SMLL-20-2404211-g007.jpg

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