通过纳米材料诱导铁变态反应:癌症治疗的有效新途径

M. Ensoy, İlayda Öztürk, D. Cansaran-Duman, Açelya Yilmazer
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摘要

利用纳米材料诱导癌症铁变态反应为研究和临床应用提供了一条前景广阔的途径。纳米材料的独特性能,如体积小、比表面积大、可针对特定任务进行设计等,使其成为诱导癌症铁突变疗法的理想候选材料。铁突变是一种新型的细胞死亡机制,有别于细胞凋亡和坏死。它已被证明在治疗各种肿瘤中至关重要。铁凋亡机制主要与细胞的铁、氨基酸、谷胱甘肽和脂质代谢调节有关。近年来,铁突变机制与癌症纳米药物之间的关系引起了人们的极大兴趣。据报道,纳米药物与铁突变的结合可在治疗不同类型的癌症方面取得很高的疗效。本综述将概述近年来与铁突变相关的癌症纳米医学研究工作。首先,概述了铁凋亡的定义及其与其他细胞死亡机制的区别。随后,将详细讨论在癌症纳米医学领域探索铁突变作用的研究。其中特别强调了组合治疗策略的使用,这些策略将铁突变与化学动力疗法、光动力疗法、光热疗法、免疫疗法和声动力疗法相结合。考虑到诱导铁细胞减少症的纳米粒子已被引入临床研究,纳米科学家可以通过调整纳米材料的理化特性进一步加快临床转化。这篇综述为所有对铁变态反应与癌症导向纳米粒子之间的分子特征和关系感兴趣的研究人员提供了启发性信息。
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Inducing ferroptosis via nanomaterials: a novel and effective route in cancer therapy
The use of nanomaterials for cancer ferroptosis presents a promising avenue for research and clinical applications. The unique properties of nanomaterials, such as their small size, large surface area, and ability to be engineered for specific tasks, make them ideal candidates for ferroptosis inducing cancer therapies. Ferroptosis is a new type of cell death mechanism that is distinct from apoptosis and necrosis. It has been shown to be critical in the treatment of various tumors. The ferroptotic mechanism has been mainly linked with the regulation of iron, amino acid, glutathione, and lipid metabolism of cells. The relationship between ferroptosis mechanisms and cancer nanomedicine has attracted considerable interest in recent years. It has been reported that the combination of nanomedicine and ferroptosis can achieve high therapeutic efficacy for the treatment of different cancer types. This review will provide an overview of recent work in ferroptosis-related cancer nanomedicine. First, general information is given about the definition of ferroptosis and its differences from other cell death mechanisms. Later, studies exploring the role of ferroptosis in the cancer nanomedicine field are discussed in detail. Specific focus has been given to the use of combinatorial treatment strategies which combine ferroptosis with chemodynamic therapy, photodynamic therapy, photothermal therapy, immunotherapy and sonodynamic therapy. Considering the fact that ferroptosis inducing nanoparticles have already been introduced into clinical studies, nanoscientists can further accelerate this clinical translation as they tailor the physicochemical characteristics of nanomaterials. This review provides enlightening information for all researchers interested in the molecular characterization and relationship between ferroptosis and cancer-directed nanoparticles.
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