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 stage-driven disruption of NK cell maturation in human and murine tumors.
Tumor stage-driven disruption of NK cell maturation in human and murine tumors.
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自然杀伤(NK)细胞在对抗癌症中发挥关键作用,既通过直接杀伤恶性细胞,也通过分泌细胞因子和趋化因子促进适应性免疫应答。在肺部肿瘤微环境(TME)中,NK细胞稀少且功能失调。通过对肺部肿瘤进行单细胞转录组分析,并探索拟时序,我们发现NK细胞的瘤内成熟轨迹以肿瘤分期依赖的方式受到破坏,最终导致细胞毒性亚群的选择性排除。利用功能实验,我们观察到瘤内NK细胞死亡以及细胞毒性能力的降低取决于肿瘤分期。最后,我们对人类肺癌公共数据集的分析证实了这些发现,揭示了肿瘤进展过程中NK细胞存在类似的成熟功能障碍过程。这些结果突出了肿瘤细胞逃逸NK细胞细胞毒性的额外机制,从而为定制治疗策略铺平了道路。
Natural killer (NK) cells play a pivotal role against cancer, both by direct killing of malignant cells and by promoting adaptive immune response though cytokine and chemokine secretion. In the lung tumor microenvironment (TME), NK cells are scarce and dysfunctional.
By conducting single-cell transcriptomic analysis of lung tumors, and exploring pseudotime, we uncovered that the intratumoral maturation trajectory of NK cells is disrupted in a tumor stage-dependent manner, ultimately resulting in the selective exclusion of the cytotoxic subset. Using functional assays, we observed intratumoral NK cell death and a reduction in cytotoxic capacities depending on the tumor stage.
Finally, our analyses of human public dataset on lung cancer corroborate these findings, revealing a parallel dysfunctional maturation process of NK cells during tumor progression. These results highlight additional mechanisms by which tumor cells escape from NK cell cytotoxicity, therefore paving the way for tailored therapeutic strategies.
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