Targeting Ferroptosis for Cancer Immunotherapy: Molecular Mechanisms, Immune Microenvironment Crosstalk, and Clinical Translation Prospects

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Jiamin Shi, Guoren Zhou
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引用次数: 0

Abstract

Ferroptosis, a novel form of iron-dependent programmed cell death (PCD), has garnered extensive attention in the cancer research field in recent years. Through its unique iron-dependent regulatory mechanisms and dynamic crosstalk with the cancer immune microenvironment (CIME), ferroptosis has established a new research paradigm for cancer therapy. This review systematically clarifies the molecular mechanisms underlying ferroptosis, thoroughly explores its dual regulatory roles within the CIME, and elaborates on the reciprocal interactions between ferroptosis and immune cell functions. It also comprehensively discusses ferroptosis-based cancer immunotherapy strategies and their clinical translation prospects. By integrating the latest research advances, this work provides a theoretical foundation and practical guidance for the clinical application of ferroptosis in cancer immunotherapy.

针对铁下垂的癌症免疫治疗:分子机制、免疫微环境串扰和临床转化前景
铁凋亡是一种新型的铁依赖性程序性细胞死亡(PCD),近年来引起了癌症研究领域的广泛关注。通过其独特的铁依赖性调节机制和与癌症免疫微环境(CIME)的动态串扰,铁上垂症为癌症治疗建立了新的研究范式。本文系统阐明了铁下垂的分子机制,深入探讨了铁下垂在CIME中的双重调控作用,并阐述了铁下垂与免疫细胞功能之间的相互作用。本文还全面讨论了基于铁中毒的癌症免疫治疗策略及其临床应用前景。通过整合最新的研究进展,本工作为铁下垂在肿瘤免疫治疗中的临床应用提供了理论基础和实践指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advanced Therapeutics
Advanced Therapeutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.10
自引率
2.20%
发文量
130
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