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:Aurantii Fructus Immaturus enhances natural killer cytolytic activity and anticancer efficacy in vitro and in vivo.
Aurantii Fructus Immaturus enhances natural killer cytolytic activity and anticancer efficacy in vitro and in vivo.
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枳实(AFI)在传统草药中被广泛使用,已知对多种疾病具有多样的生理效应,包括肥胖、糖尿病和心血管疾病。然而,AFI对免疫系统,尤其是自然杀伤(NK)细胞的影响,仍很大程度上未知。
我们旨在研究AFI在体外和体内对NK细胞活性的影响,并阐明其潜在机制。此外,我们在小鼠肺转移模型中验证了AFI的抗癌疗效,强调了AFI在癌症治疗中的治疗潜力。
我们的结果显示,AFI以剂量依赖性方式显著增强NK细胞的细胞溶解活性,伴随NK细胞活化受体表达增加,尤其是NKp30和NKp46。AFI处理还增加了细胞溶解颗粒的表达,包括颗粒酶B和穿孔素。
此外,脱颗粒标志物CD107a的表达在AFI处理后增加。使用western blot分析的信号传导研究表明,细胞外信号调节激酶(ERK)的磷酸化参与了AFI处理后NK细胞活性的增加。在小鼠体内研究中,口服给予AFI显著增强了脾单核细胞对YAC-1细胞的细胞毒性活性,伴随NKp46上调。
此外,我们证实,在使用小鼠黑色素瘤B16F10细胞系建立的小鼠癌症转移模型中,通过体内给予AFI,癌症转移受到抑制。总之,这些结果表明AFI通过激活ERK信号通路在体外和体内增强NK细胞介导的细胞毒性,并提示AFI可能成为癌症免疫治疗的潜在补充剂。
Aurantii Fructus Immaturus (AFI), extensively used in traditional herbal medicine, is known to have diverse physiological effects against various diseases, including obesity, diabetes, and cardiovascular disease.
However, the effects of AFI on the immune system, especially natural killer (NK) cells, remain largely unknown.
We aimed to investigate the effect of AFI on NK cell activity in vitro and in vivo and to elucidate the underlying mechanisms.
Further, we verified the anticancer efficacy of AFI in a mouse lung metastasis model, underscoring the therapeutic potential of AFI in cancer therapy.
Our results revealed that AFI significantly enhanced the cytolytic activity of NK cells in a dose-dependent manner, accompanied by an increase in the expression of NK cell-activating receptors, especially NKp30 and NKp46. AFI treatment also increased the expression of cytolytic granules, including granzyme B and perforin.
Furthermore, the expression of CD107a, a degranulation marker, was increased upon treatment with AFI. A signaling study using western blot analysis demonstrated that the phosphorylation of extracellular signal-regulated kinase (ERK) was involved in increasing the NK cell activity following AFI treatment. In the in vivo study performed in mice, oral administration of AFI markedly enhanced the cytotoxic activity of spleen mononuclear cells against YAC-1 cells, which was accompanied by NKp46 upregulation.
In addition, we confirmed that cancer metastasis was inhibited in a mouse cancer metastasis model, established using the mouse melanoma B16F10 cell line, by the administration of AFI in vivo. Collectively, these results indicate that AFI enhances NK cell-mediated cytotoxicity in vitro and in vivo via activation of the ERK signaling pathway and suggest that AFI could be a potential supplement for cancer immunotherapy.
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