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:Reversing NK cell exhaustion: a novel strategy combining immune checkpoint blockade with drug sensitivity enhancement in the treatment of hepatocellular carcinoma.
Reversing NK cell exhaustion: a novel strategy combining immune checkpoint blockade with drug sensitivity enhancement in the treatment of hepatocellular carcinoma.
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肝细胞癌(HCC)是全球最常见的致死性癌症之一。NK 细胞(NK细胞)在肝脏免疫监视中发挥关键作用,但在肿瘤微环境中,NK细胞容易发生耗竭,表现为活化受体下调、细胞因子分泌减少和杀伤功能减弱。抑制性受体如PD-1、TIM-3和LAG-3的上调进一步加剧了NK细胞的耗竭。针对这些免疫抑制机制的联合阻断策略,如PD-1抑制剂与其他抑制性通路(如TIM-3和LAG-3)的联合,已在临床前研究中显示出逆转NK细胞耗竭的潜力。本文探讨了这些创新策略在HCC免疫治疗中的前景,为优化NK细胞功能和改善药物敏感性提供了新的治疗方向。
Hepatocellular carcinoma (HCC) is one of the most common lethal cancers worldwide. Natural killer cells (NK cells) play a key role in liver immunosurveillance, but in the tumor microenvironment, NK cells are readily depleted, as evidenced by down-regulation of activating receptors, reduced cytokine secretion, and attenuated killing function. The up-regulation of inhibitory receptors, such as PD-1, TIM-3, and LAG-3, further exacerbates the depletion of NK cells.
Combined blockade strategies targeting these immunosuppressive mechanisms, such as the combination of PD-1 inhibitors with other inhibitory pathways (eg. TIM-3 and LAG-3), have shown potential to reverse NK cell exhaustion in preclinical studies. This article explores the promise of these innovative strategies in HCC immunotherapy, providing new therapeutic directions for optimizing NK cell function and improving drug sensitivity.
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