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:Tumor microenvironment-driven natural killer cell diversity: mechanisms and therapeutic opportunities.
Tumor microenvironment-driven natural killer cell diversity: mechanisms and therapeutic opportunities.
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自然杀伤(NK)细胞是参与肿瘤免疫监视的关键效应细胞,然而其在肿瘤微环境(TME)中的功能表现出相当大的复杂性和可塑性,无法用经典的CD56/CD16二分法充分解释。这种功能多样性源于受TME塑造的不同NK细胞亚群的表型适应性和动态分化。在本综述中,我们系统性地探讨了TME中新近发现的NK细胞亚群的定义特征和功能作用;阐明了调控它们的分子机制;并强调了这些亚群之间的功能转变和协同相互作用。此外,基于当前证据,我们总结了靶向特定NK细胞亚群的新兴免疫治疗方法。总之,这些观点为解析NK细胞在抗肿瘤免疫中的多方面作用以及推进亚群靶向疗法的开发提供了新见解和战略方向。
Natural killer (NK) cells are key effector cells involved in tumor immune surveillance, yet their function within the tumor microenvironment (TME) exhibits considerable complexity and plasticity that cannot be adequately explained by the classical CD56/CD16 dichotomy. This functional diversity arises from the phenotypic adaptability and dynamic differentiation of distinct NK cell subsets shaped by the TME.
In this review, we systematically examine the defining characteristics and functional roles of recently identified NK cell subsets in the TME; elucidate the molecular mechanisms governing their regulation; and highlight the functional transitions and cooperative interactions among these subsets.
Moreover, building on current evidence, we summarize emerging immunotherapeutic approaches targeting specific NK cell subsets.
Together, these perspectives offer new insights and strategic directions for deciphering the multifaceted roles of NK cells in antitumor immunity and advancing the development of subset-targeted therapies.
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