Zou Yutao, Wu Junjie, Zhang Qiuyun, Chen Jiayi, Luo Xuanxuan, Qu Yijie, Xia Rui, Wang Weiqi, Zheng Xiaohua
The People's Hospital of Danyang, Affiliated Danyang Hospital of Nantong University, Danyang, Jiangsu, China.
School of Pharmacy, Nantong University, Nantong, Jiangsu, China.
Front Pharmacol. 2024 Dec 4;15:1505212. doi: 10.3389/fphar.2024.1505212. eCollection 2024.
Porphyrins-based nanoscale metal-organic frameworks (nMOFs) has been widely utilized to kills tumor cells by generating cytotoxic reactive oxygen species (ROS). However, porphyrin based nMOFs (por-nMOFs) still face challenges such as rapid immune clearance and weak tumor targeting. Researchers have discovered that using a top-down biomimetic strategy, where nMOFs are coated with cell membranes, can promote long blood circulation, evade the reticuloendothelial system, and improve cancer cell targeting, thereby significantly enhancing the photodynamic therapy (PDT) effect of nMOFs. This review summarizes the recent work on different cell membranes-coated por-nMOFs for enhanced tumor PDT. This review details the changes in physicochemical properties, enhanced homotypic cancer cell-selective endocytosis, improved tumor tissue targeting, and increased cytotoxicity and effective tumor suppression after the nMOFs are wrapped with cell membranes. Additionally, this review compares the biological functions of various types of cell membranes, including cancer cell membranes, red blood cell membranes, aptamer-modified red blood cell membranes, and hybrid membranes from the fusion of cancer and immune cells. The review highlights the enhanced immunogenic cell death function when using hybrid membranes derived from the fusion of cancer and immune cell membranes. By summarizing the augmented PDT effects and the combined antitumor outcomes with other therapeutic modalities, this review aims to provide new insights into the biomedical applications of por-nMOFs and offer more references for the preclinical application of porphyrin-based photosensitizers.
基于卟啉的纳米级金属有机框架(nMOF)已被广泛用于通过产生活性细胞毒性氧物种(ROS)来杀死肿瘤细胞。然而,基于卟啉的nMOF(por-nMOF)仍然面临诸如快速免疫清除和弱肿瘤靶向性等挑战。研究人员发现,采用自上而下的仿生策略,即nMOF用细胞膜包覆,可以促进血液循环时间延长、避开网状内皮系统并改善癌细胞靶向性,从而显著增强nMOF的光动力疗法(PDT)效果。本综述总结了近期关于不同细胞膜包覆的por-nMOF用于增强肿瘤PDT的研究工作。本综述详细介绍了nMOF被细胞膜包裹后其物理化学性质的变化、增强的同型癌细胞选择性内吞作用、改善的肿瘤组织靶向性以及增加的细胞毒性和有效的肿瘤抑制作用。此外,本综述比较了各种类型细胞膜的生物学功能,包括癌细胞膜、红细胞膜、适配体修饰的红细胞膜以及癌细胞与免疫细胞融合产生的杂交膜。该综述强调了使用癌细胞与免疫细胞膜融合产生的杂交膜时增强的免疫原性细胞死亡功能。通过总结增强的PDT效果以及与其他治疗方式联合的抗肿瘤结果,本综述旨在为por-nMOF的生物医学应用提供新见解,并为基于卟啉的光敏剂的临床前应用提供更多参考。