RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Macrophage barrier in the tumor microenvironment and potential clinical applications.
Macrophage barrier in the tumor microenvironment and potential clinical applications.
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肿瘤微环境(TME)构成了一个复杂的微环境,包含多种免疫细胞和基质成分。在这一复杂的背景下,肿瘤相关巨噬细胞(TAMs)表现出显著的空间异质性。这种异质性促成了肿瘤行为的多个方面,包括免疫反应调节、血管生成、组织重塑和转移潜能。本综述总结了巨噬细胞在生理环境和TME中的空间分布。此外,本文探讨了TAMs与TME中多种免疫细胞群(T细胞、树突状细胞、中性粒细胞、NK 细胞及其他免疫细胞)之间复杂的相互作用。这些双向交流形成了复杂的免疫相互作用网络,影响肿瘤免疫监视和免疫逃逸策略。研究TAM异质性及其与不同免疫细胞群的复杂相互作用,为治疗干预提供了潜在途径。此外,本文讨论了靶向巨噬细胞的治疗策略,旨在揭示免疫治疗的新方法。视频摘要。
The tumor microenvironment (TME) constitutes a complex microenvironment comprising a diverse array of immune cells and stromal components. Within this intricate context, tumor-associated macrophages (TAMs) exhibit notable spatial heterogeneity. This heterogeneity contributes to various facets of tumor behavior, including immune response modulation, angiogenesis, tissue remodeling, and metastatic potential. This review summarizes the spatial distribution of macrophages in both the physiological environment and the TME.
Moreover, this paper explores the intricate interactions between TAMs and diverse immune cell populations (T cells, dendritic cells, neutrophils, natural killer cells, and other immune cells) within the TME. These bidirectional exchanges form a complex network of immune interactions that influence tumor immune surveillance and evasion strategies. Investigating TAM heterogeneity and its intricate interactions with different immune cell populations offers potential avenues for therapeutic interventions.
Additionally, this paper discusses therapeutic strategies targeting macrophages, aiming to uncover novel approaches for immunotherapy. Video Abstract.
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