纳米药物靶向缺氧信号通路逆转免疫治疗耐药。

IF 4.6 Q1 ONCOLOGY
癌症耐药(英文) Pub Date : 2025-09-02 eCollection Date: 2025-01-01 DOI:10.20517/cdr.2025.132
Xiaoliang Cheng, Peixing Wang, Hongqiang Lyu, Yonghyun Lee, Juyoung Yoon, Haiyan Dong
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引用次数: 0

摘要

免疫疗法已成为癌症的主要治疗策略;然而,免疫治疗耐药性仍然是一个重大挑战。缺氧是肿瘤微环境的一个关键标志,它是由快速增殖的癌细胞的高氧需求与异常血管的有限供应之间的不平衡造成的,在驱动免疫治疗抵抗中起着核心作用。缺氧诱导因子-1α (HIF-1α)及其下游信号通路通过促进巨噬细胞向致瘤性M2表型极化、诱导T细胞衰竭、促进免疫逃避、增强血管生成和激活其他抵抗机制参与这种抵抗。这篇综述强调了缺氧调节免疫治疗抵抗的机制,并提供了基于纳米技术的策略的全面概述,旨在对抗缺氧诱导的抵抗。最后,概述了将基于纳米药物的药物输送系统转化为克服免疫治疗耐药性的临床实践的前景和挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting the hypoxia signaling pathway with nanomedicine to reverse immunotherapy resistance.

Immunotherapy has emerged as a major therapeutic strategy for cancer; however, immunotherapy resistance remains a significant challenge. Hypoxia, a key hallmark of the tumor microenvironment resulting from the imbalance between the high oxygen demand of rapidly proliferating cancer cells and the limited supply from abnormal blood vessels, plays a central role in driving immunotherapy resistance. Hypoxia-inducible factor-1α (HIF-1α) and its downstream signaling pathways contribute to this resistance by promoting macrophage polarization toward the protumorigenic M2 phenotype, inducing T cell exhaustion, facilitating immune evasion, enhancing angiogenesis, and activating other resistance mechanisms. The review highlights the mechanisms by which hypoxia regulates resistance to immunotherapy and provides a comprehensive overview of nanotechnology-based strategies designed to counteract hypoxia-induced resistance. Finally, the prospects and challenges of translating nanomedicine-based drug delivery systems into clinical practice for overcoming immunotherapy resistance are outlined.

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