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-responsive manganese-based nano-modulator activate the cGAS-STING pathway to enhance innate immune system response.
Tumor microenvironment-responsive manganese-based nano-modulator activate the cGAS-STING pathway to enhance innate immune system response.
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这种 HA 修饰的锰基混合纳米调节剂可通过增强先天免疫活性来增强抗肿瘤治疗,并可能为癌症的免疫治疗和临床转化提供新方向。
锰离子(Mn2+)与能够损伤和裂解肿瘤细胞的佐剂结合,形成一种抗肿瘤纳米调节剂,通过环鸟苷酸-腺苷酸干扰素基因合成酶-刺激因子(cGAS-STING)通路的级联激活,增强癌症治疗的免疫疗效,这凸显了开发抗肿瘤纳米调节剂的重要性,此类调节剂可诱导DNA损伤并增强cGAS-STING活性,是未来关键的研究方向。
我们成功合成了一种抗肿瘤纳米调节剂,其具有良好的分散性和生物安全性。该纳米调节剂通过将二氧化锰纳米片(M-NS)负载已知具有免疫原性增强作用的zebularine(Zeb),并使用透明质酸(HA)进行靶向表面修饰而构建。经体循环到达肿瘤部位后,Mn2+、Zeb和活性氧(ROS)在肿瘤微环境中由H+和H2O2催化释放。这些组分可直接或间接损伤肿瘤细胞的DNA或线粒体,从而诱导程序性细胞死亡。此外,它们促进双链DNA(dsDNA)在细胞质中的积累,增强cGAS-STING信号通路的激活,并促进I型干扰素的产生和促炎细胞因子的分泌。另外,Zeb@MH-NS增强树突状细胞的成熟、细胞毒性T淋巴细胞的浸润以及肿瘤部位NK 细胞的募集。
Manganese ions (Mn 2+ ) combined with adjuvants capable of damaging and lysing tumor cells form an antitumor nano-modulator that enhances the immune efficacy of cancer therapy through the cascade activation of the cyclic GMP-AMP interferon gene synthase-stimulator (cGAS-STING) pathway, which underscores the importance of developing antitumor nano-modulators, which induce DNA damage and augment cGAS-STING activity, as a critical future research direction. METHODS AND RESULTS: We have successfully synthesized an antitumor nano-modulator, which exhibits good dispersibility and biosafety. This nano-modulator is engineered by loading manganese dioxide nanosheets (M-NS) with zebularine (Zeb), known for its immunogenicity-enhancing effects, and conducting targeted surface modification using hyaluronic acid (HA). After systemic circulation to the tumor site, Mn 2+ , Zeb, and reactive oxygen species (ROS) are catalytically released in the tumor microenvironment by H + and H 2 O 2. These components can directly or indirectly damage the DNA or mitochondria of tumor cells, thereby inducing programmed cell death. Furthermore, they promote the accumulation of double-stranded DNA (dsDNA) in the cytoplasm, enhancing the activation of the cGAS-STING signalling pathway and boosting the production of type I interferon and the secretion of pro-inflammatory cytokines. Additionally, Zeb@MH-NS enhances the maturation of dendritic cells, the infiltration of cytotoxic T lymphocytes, and the recruitment of natural killer cells at the tumor site.
This HA-modified manganese-based hybrid nano-regulator can enhance antitumor therapy by boosting innate immune activity and may provide new directions for immunotherapy and clinical translation in cancer.
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