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:The stress response regulator HSF1 modulates natural killer cell anti-tumour immunity.
The stress response regulator HSF1 modulates natural killer cell anti-tumour immunity.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
多种细胞损伤均汇聚于热休克因子1(HSF1)的激活,HSF1调控蛋白质毒性应激反应以维持蛋白质稳态。HSF1以细胞类型和情境特异性的方式调控蛋白质毒性应激反应之外的众多基因程序,从而促进恶性肿瘤。然而,HSF1在肿瘤微环境免疫群体中的作用仍不明确。在此,我们利用HSF1激活的体内模型和单细胞转录组肿瘤分析,证明自然杀伤(NK)细胞中HSF1活性增强会损害细胞毒性、细胞因子产生及随后的抗肿瘤免疫。在机制上,HSF1直接结合并调控NK细胞效应功能关键介质的表达。这项工作表明,HSF1在肿瘤微环境的应激条件下调控免疫反应。这些发现对于提高过继性NK细胞疗法的疗效以及设计包括NK细胞介导肿瘤杀伤调节剂在内的联合策略具有重要意义。
Diverse cellular insults converge on activation of the heat shock factor 1 (HSF1), which regulates the proteotoxic stress response to maintain protein homoeostasis. HSF1 regulates numerous gene programmes beyond the proteotoxic stress response in a cell-type- and context-specific manner to promote malignancy.
However, the role(s) of HSF1 in immune populations of the tumour microenvironment remain elusive.
Here, we leverage an in vivo model of HSF1 activation and single-cell transcriptomic tumour profiling to show that augmented HSF1 activity in natural killer (NK) cells impairs cytotoxicity, cytokine production and subsequent anti-tumour immunity.
Mechanistically, HSF1 directly binds and regulates the expression of key mediators of NK cell effector function. This work demonstrates that HSF1 regulates the immune response under the stress conditions of the tumour microenvironment.
These findings have important implications for enhancing the efficacy of adoptive NK cell therapies and for designing combinatorial strategies including modulators of NK cell-mediated tumour killing.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。